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Daily Archives: November 10, 2016
Voices for Reason Blog | The Ayn Rand Institute
Posted: November 10, 2016 at 5:42 pm
POST by The Editors| View all Posts November 09, 2016
Thanks to our contributors, ARI is able to show students how Ayn Rands ideas can empower them to live free and thrive in a big way.
In this episode of The Yaron Brook Show, Yaron Brook comments on the unusually intellectual response to his talks in Europe and illustrates how philosophy shapes history, particularly the positive impact of Aristotles ideas. Also, Brook discusses why he wont debate Stefan Molyneux, the political and economical state of Greece, race realism and free will.
The rich are getting richer in a system rigged in their favor. True or false? Hear two sides of the economic inequality story in the upcoming debate between Yaron Brook, ARI executive chairman, and Jonathan Haughton, Beacon Hill Institute senior economist.
The 2016 Ayn Rand Student Conference in Atlanta, Georgia, is about to begin.
Why is voter rage so rampant? What has brought out this ugliness and hate? How can you exercise your rights and keep out of the emotionalism plaguing America?
Join Tara Smith, ARI board member and professor of philosophy at the University of Texas at Austin, for a panel discussion of her latest book Judicial Review in an Objective Legal System.
This talk examines the development, operation and performance of monetary systems in the absence of government intervention. Topics covered include the spontaneous evolution of money, the rise of banks, bank self-regulation under competition and crisis management in the absence of a central bank.
What exactly is globalism? Are trade deals like NAFTA desirable? Should one go into politics? Is tuition-free college education a good idea?
What do you call a payment of money for the release of a prisoner? Yes, its a ransom. But not if the recipient is Iran. That, the Obama administration calls a triumph of diplomacy.
It looks like the upcoming 2016 Ayn Rand Student Conference is going to be the largest student Objectivist conference ever. The conferences theme is free will. But what exactly is free will? Does it even exist? How do you know? Whats the Objectivist perspective? And what implications, if any, does it have for how you live your life?
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13 Nootropics to Unlock Your True Brain – blog.bulletproof.com
Posted: at 5:37 pm
Nootropics sometimes calledsmart drugs are compounds that enhance brain function. Theyre becoming a popular way to give your mind an extra boost. According to one Telegraph report, up to 25% of students at leading UK universities have taken the prescription smart drug modafinil [1], and California tech startup employees are trying everything from Adderall to LSD to push their brains into a higher gear [2].
Ive been actively benefitting from nootropics since 1997, when I was struggling with cognitive performance and ordered almost $1000 worth of smart drugs from Europe (the only place where you could get them at the time). I remember opening the unmarked brown package and wondering whether the pharmaceuticals and natural substances would really enhance my brain.
They did, and Ive been a big fan of certain cognitive enhancers ever since.
Im wary of others, though. The trouble with using a blanket term like nootropics is that you lump all kinds of substances in together. Technically, you could argue that caffeine and cocaine are both nootropics, but theyre hardly equal. With so many ways to enhance your brain function, many of which have significant risks, its most valuable to look at nootropics on a case-by-case basis. Heres a list of 13 nootropics, along with my thoughts on each.
I started taking modafinil while getting my MBA at Wharton. I was also working at a start-up that later sold for $600 million in value, so you can imagine how busy I was. I wanted a way to keep my brain running.
When I first started taking modafinil, I felt more like myself than I had in years. I took it just about every day in varying doses for 8 years (with a physicians prescription). It gave me energy and changed my life. I would not be the biohacker I am today without modafinil.
When I worked on the Bulletproof Diet book, I wanted to verify that the effects I was getting from Bulletproof Coffee were not coming from modafinil, so I stopped using it and measured my cognitive performance while I was off of it. What I found was that on Bulletproof Coffee and the Bulletproof Diet, my mental performance was almost identical to my performance on modafinil. I still travel with modafinil, and Ill take it on occasion, but while living a Bulletproof lifestyle I rarely feel the need.
Theres a slight risk (about 5 in a million people) of having a life-threatening immune reaction to modafinil. Its the same reaction that happens with ibuprofen and other NSAIDs (non-steroidal anti-inflammatory drugs), so if you know you dont react well to NSAIDs, talk to your doctor before taking modafinil.
One reason I like modafinil is that it enhances dopamine release, but it binds to your dopamine receptors differently than addictive substances like cocaine and amphetamines do, which may be part of the reason modafinil shares many of the benefits of other stimulants but doesnt cause addiction or withdrawal symptoms [3,4]. It does increase focus, problem-solving abilities, and wakefulness, but it is not in the same class of drugs as Adderall, and it is not a classical stimulant. Modafinil is off of patent, so you can get it generically, or order it from India. Its a prescription drug, so you need to talk to a physician.
You can also try armodafinil, which is a more purified form of modafinil with only biologically identical molecules in it. It has nearly identical and sometimes stronger effects. Its very expensive without insurance.
If you dont want to get a prescription, theresadrafinil, which your liver converts to modafinil in about 45-60 minutes. You can buy adrafinil without a prescription, and in my experience it feels very similar to modafinil, but I wouldnt recommend taking it regularly because it stresses your liver a lot.
Normally prescribed modafinil dose: 50-200 mg, taken in the morning (unless you want to be awake all night)
Normally prescribed arrmodafinil dose: 100-200 mg, taken in the morning
Adrafinil dose: 300 mg, taken in the morning
The racetam family contains dozens of related compounds, includinga few well-known nootropics. The best studied one is piracetam, but the most effective nootropics are aniracetam and phenylpiracetam, so youll read about those here.
There was an explosion of racetam research between 1968 and 1972, but many of the racetams are off patents, so pharmaceutical companies are studying racetam analogs that they can patent and sell. We still dont fully understand how racetams work, but theres plenty of anecdotal evidence that theyre excellent nootropics. The best studied racetam is piracetam, and its analogs work well too.
I like aniracetam more than piracetam because its the only member of the racetam that has a stress-lowering effect and also increase memory IO (getting memories in and out of your mind). I take aniracetam every day, as well as for public speaking. I find I speak more fluently (no ums or ahs) and I dont have to grasp for words. I find that phenylpiracetam improves my learning, memory, and energy, too.
I dont use piracetam or oxiracetam because theyre weaker forms of phenylpiracetam and aniracetam. I suggest you try racetams alone at first not in a pre-made stack because ones that work for other people may not work for you. For example, I feel nothing from noopept (a very strong derivative of piracetam), but I know plenty of people for whom it works very well.
Racetams are very bitter, so its best to get them in capsules. In some people they deplete acetylcholine [10], which can cause headaches. If that happens, try adding in Choline Force or a raw pastured egg yolk to give your body the materials to make more acetylcholine. You can also try lowering doses; too much can make you irritable.
These nootropics sound a little unusual, but Ive been on them every day since 1997 and theyre a core part of my nootropic stack. It irritates me that theyre in a regulatory gray zone.
One last thing: these phenylpiracetam, aniracetam, and noopept are all fat soluble, so take them with a meal or a fat source (like your morning Bulletproof Coffee) to increase their absorption.
Phenylpiracetam dose: 100 mg, 1-4 times daily
Aniracetam dose: 650 mg, 1-2 times daily
Noopept dose: 10 mg, 1-2 times daily
Nicotine can be a powerful nootropic if you take it carefully and sparingly. Heres a full guide to using nicotine as a nootropic, complete with pros and cons, risks, dose recommendations, and advice about what form of nicotine to use.
I do NOT recommend smoking cigarettes or using tobacco to get your nicotine. Im talking about very small doses that are far lower than youd get from smoking. Nicotine has a direct effect on your mitochondrial energy, and just about anything that increases mitochondrial function is going to make your brain work better.
Big Pharma has recommended amphetamine (Adderall) for ADHD sufferers for years now. Its also popular on college campuses around exam time. Too bad, because there are much better choices.
Amphetamine has substantial risks. In healthy adults, itimproves attention, focus, motivation to work, and short-term memory, all by increasing dopamine and norepinephrine release in your prefrontal cortex [11,12]. Amphetamine also decreases fatigue, but it makes you jittery and can increase anxiety.
What worries me about amphetamine is its addictive potential, and the fact that it can cause stress and anxiety. Research says its only slightly likely to cause addiction in people with ADHD [13], but we dont know much about its addictive potential in healthy adults. We all know the addictive potential of methamphetamine, and amphetamine is closely related enough to make me nervous about so many people giving it to their children. Amphetamines cause withdrawal symptoms, so the potential for addiction is there.
If you want a stimulant, drink coffee. If you want something stronger, try a racetam or talk to your doctor about modafinil. If you do decide to take Adderall, youll need a prescription but I really recommend avoiding it. There are many better options out there.
L-theanine is a major component of black and green tea. On its own, theanine promotes relaxation [14], alertness, and arousal [15].
Theanine also works synergistically with caffeine. Together, the two increase reaction time, memory, and mental endurance [16].
You can get your theanine from a capsule, or you can drink a cup or two of green tea. If you decide to do the green tea, look for tea thats grown in the shade, because shade-grown green tea typically has much higher levels of theanine.
L-theanine dose: 50-200 mg. You can take it with your morning coffee, or you can take it at night, like me.
Bacopa monnieri is a small water plant native to India. Bacopais an adaptogen it helps your body adapt to stress. It also improves memory in healthy adults [17] and enhances attention and mood in people over 65 [18]. Scientists still dont fully understand how Bacopa works, but they do know it takes time to work; study participants didnt feel its memory-enhancing effects until theyd been supplementing with it daily for 4 weeks, so if you try Bacopa, stick with it for a month before you give up on it.
Bacopa suppresses sperm production in male mice, so you may want to skip it if youre trying to conceive [19]. It didnt affect the mices testosterone or sex drive, though.
A lot of nootropic companies include Bacopa in their stacks, but they often dont use enough to give you real benefits. You want at least 750 mg daily. Take Bacopa with a fat source to increase its absorption.
Bacopa monnieri dose: At least 750 mg daily, taken with a source of fat
Yes, were talking 1960s, Jimi Hendrix, psychedelic LSD. Dr. Rick Doblin and I have discussed the use of psychedelic medicine on Bulletproof Radio before. Now, Silicon Valley tech employees are reporting benefits from using LSD as a nootropic, but it has a history of being misused by both governments and partiers. (In fact, Bulletproof Radio guest Jan Irwin has published lots of research showing that much of the psychedelic movement is at least partly the result of government initiatives.)
The key to using LSD as a nootropic, according to the Silicon Valley techies, is getting the right dose. They say that when they take microdoses about 1/10th of a recreational dose they experience increased positivity, creativity, focus, and empathy.
LSD as a nootropic may not be as crazy as it sounds. Its certainly a mind-expanding drug, and studies suggest that its less risky than its reputation suggests. Even at a full dose (again, 10 times a microdose), researchers ranked LSD the 4th least dangerous common recreational drug far below alcohol and nicotine [20] and historically not a single person has died from LSD overdose [21]. Its possible to react poorly to LSDs psychological effects, but microdoses are below the dose that usually causes hallucinations [22]. LSD does increase your suggestibility, so you should be extra aware of making big decisions if you are using it as a nootropic.
LSD dose: 10 micrograms, taken in the morning, every 3 days. (This is probably illegal where you live. Its experimental but shows great promise from anecdotal reports. I look forward to the day when its legal for researchers to actually determine how impactful this is. Until the government allows this kind of research in your country, the only option is to wait, or to be your own guinea pig. Be safe if you experiment with anything.)
Unfair Advantage supports your mitochondria, the power plants of your cells, with two different ingredients:
You have the highest density of mitochondria in your brains prefrontal cortex, which helps to explain why I feel Unfair Advantage in my head first. You have the second highest density in your heart, which is probably why I feel it in the center of my chest next. Mitochondrial energizers can have profound nootropic effects! At higher doses mitochondrial energizers also make for an excellent pre-workout supplements.
Unfair Advantage dose: 1-4 ampules, taken any time
Bulletproof Upgraded Aging Formula is another powerful nootropic. It contains oxaloacetate, a neuroprotective agent that can shield your brain from environmental toxins. Oxaloacetate also decreases brain inflammation [25].
Common environmental toxins pesticides, for example cause your brain to release glutamate (a neurotransmitter). Your brain needs glutamate to function, but when you create too much of it it becomes toxic and starts killing neurons. The oxaloacetate in Upgraded Aging protects rodents from glutamate-induced brain damage [26]. Oxaloacetate also promotes brain recovery after stress or trauma [27, 28].
Upgraded Aging is a great way to give your brain a little extra protection from stress and toxins. In animal studies, it also modifies the Krebs Cycle, shifting the ratio of NADH to NAD+, which makes mitochondrial energy production more efficient.
Upgraded Aging dose: 1 capsule, taken in the morning
Forskolin has been a part of Indian Ayurvedic medicine for thousands of years. In addition to being fun to say, forskolin increases cyclic adenosine monophosphate (cAMP), a molecule essential to learning and memory formation [29].
I have used forskolin for more than a decade.
Forskolin is especially effective if you combine it with artichoke extract. Artichoke extract inhibits PDE4, an enzyme that breaks down cAMP. PDE4 inhibitors make cAMP more available, and when you add in artichoke extracts cAMP-enhancing effects, you get a significant boost to learning, memory, and motivation.
Or you get a headache and an energy crash when you come down.
That may be because upping cAMP uses more dopamine than your brain usually would. It affects different people differently. You only know if you tryit.
Bulletproof carries CILTEP, the first commercial combination of artichoke extract and forskolin. CILTEP also uses up acetylcholine, so I recommend adding in Choline Force to keep your brain well stocked.
CILTEP dose: 1-3 capsules, taken in the morning on an empty stomach
When you first start taking nootropics, sometimes youll feel like nothing is happening. Thats what I experienced. Then, a week later, I quit taking them, and noticed their absence immediately. This is because when your brain works better, it feels so natural that its hard to notice unless you have a great degree of self-awareness. On the other hand, sometimes youll feel a great cognitive boost as soon as you take a pill. That can be a good thing or a bad thing. I find, for example, that modafinil makes you more of what you already are. That means if you are already kind of a dick and you take modafinil, you might act like a really big dick and regret it. It certainly happened to me! I like to think that Ive done enough hacking of my brain that Ive gotten over that programming and that when I use nootropics they help me help people.
You can also get profoundly depressed. One of the nootropics I did not write about here, Lucidril, has superb anti-aging and cognitive benefits for some people, but others get deeply sad after taking it. After three days on Lucidril I felt entirely hopeless about my life. Fortunately, Id done my research and I stopped taking it immediately.
There is inherent risk in experimenting with pharmaceuticals, or illegal drugs like LSD. The risk is greater than it is with most natural substances. You can have a psychotic experience if you take too much LSD; youre more likely to get a big headache if you take too much of a choline stimulating herbal substance.
It also pays to check the purity of your nootropics. Ive seen some companies promoting pre-made nootropic stacks that contain ingredients like blue agave (fructose!), food coloring even pieces of metal. Read your labels!
I have great hope that medicine will wake up to the amazing benefits of nootropics and begin to incorporate them into society. Many of them not only increase your quality of life, they make your brain more resilient to the environment around you. We could all use a little more that.
Before you try nootropics, I suggest you start with the basics: get rid of the things in your diet and life that reduce cognitive performance first. That is easiest. Then, add in energizers like Brain Octane and clean up your diet. Then, go for the herbals and the natural nootropics. Use the pharmaceuticals selectively only after youve figured out your basics.
The truth is that, almost 20 years ago when my brain was failing and I was fat and tired, I did not know to follow this advice. I bought $1000 worth of smart drugs from Europe, took them all at once out of desperation, and got enough cognitive function to save my career and tackle my metabolic problems. With the information we have now, you dont need to do that. Please learn from my mistakes!
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13 Nootropics to Unlock Your True Brain - blog.bulletproof.com
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Life extension – Wikipedia
Posted: at 5:35 pm
Life extension science, also known as anti-aging medicine, indefinite life extension, experimental gerontology, and biomedical gerontology, is the study of slowing down or reversing the processes of aging to extend both the maximum and average lifespan. Some researchers in this area, and "life extensionists", "immortalists" or "longevists" (those who wish to achieve longer lives themselves), believe that future breakthroughs in tissue rejuvenation, stem cells, regenerative medicine, molecular repair, gene therapy, pharmaceuticals, and organ replacement (such as with artificial organs or xenotransplantations) will eventually enable humans to have indefinite lifespans (agerasia[1]) through complete rejuvenation to a healthy youthful condition.
The sale of purported anti-aging products such as nutrition, physical fitness, skin care, hormone replacements, vitamins, supplements and herbs is a lucrative global industry, with the US market generating about $50billion of revenue each year.[2] Some medical experts state that the use of such products has not been proven to affect the aging process and many claims regarding the efficacy of these marketed products have been roundly criticized by medical experts, including the American Medical Association.[2][3][4][5][6]
The ethical ramifications of life extension are debated by bioethicists.
During the process of aging, an organism accumulates damage to its macromolecules, cells, tissues, and organs. Specifically, aging is characterized as and thought to be caused by "genomic instability, telomere attrition, epigenetic alterations, loss of proteostasis, deregulated nutrient sensing, mitochondrial dysfunction, cellular senescence, stem cell exhaustion, and altered intercellular communication."[7]Oxidation damage to cellular contents caused by free radicals is believed to contribute to aging as well.[8][8][9]
The longest a human has ever been proven to live is 122 years, the case of Jeanne Calment who was born in 1875 and died in 1997, whereas the maximum lifespan of a wildtype mouse, commonly used as a model in research on aging, is about three years.[10] Genetic differences between humans and mice that may account for these different aging rates include differences in efficiency of DNA repair, antioxidant defenses, energy metabolism, proteostasis maintenance, and recycling mechanisms such as autophagy.[11]
Average lifespan in a population is lowered by infant and child mortality, which are frequently linked to infectious diseases or nutrition problems. Later in life, vulnerability to accidents and age-related chronic disease such as cancer or cardiovascular disease play an increasing role in mortality. Extension of expected lifespan can often be achieved by access to improved medical care, vaccinations, good diet, exercise and avoidance of hazards such as smoking.
Maximum lifespan is determined by the rate of aging for a species inherent in its genes and by environmental factors. Widely recognized methods of extending maximum lifespan in model organisms such as nematodes, fruit flies, and mice include caloric restriction, gene manipulation, and administration of pharmaceuticals.[12] Another technique uses evolutionary pressures such as breeding from only older members or altering levels of extrinsic mortality.[13][14] Some animals such as hydra, planarian flatworms, and certain sponges, corals, and jellyfish do not die of old age and exhibit potential immortality.[15][16][17][18]
Theoretically, extension of maximum lifespan in humans could be achieved by reducing the rate of aging damage by periodic replacement of damaged tissues, molecular repair or rejuvenation of deteriorated cells and tissues, reversal of harmful epigenetic changes, or the enhancement of telomerase enzyme activity.[19][20]
Research geared towards life extension strategies in various organisms is currently under way at a number of academic and private institutions. Since 2009, investigators have found ways to increase the lifespan of nematode worms and yeast by 10-fold; the record in nematodes was achieved through genetic engineering and the extension in yeast by a combination of genetic engineering and caloric restriction.[21] A 2009 review of longevity research noted: "Extrapolation from worms to mammals is risky at best, and it cannot be assumed that interventions will result in comparable life extension factors. Longevity gains from dietary restriction, or from mutations studied previously, yield smaller benefits to Drosophila than to nematodes, and smaller still to mammals. This is not unexpected, since mammals have evolved to live many times the worm's lifespan, and humans live nearly twice as long as the next longest-lived primate. From an evolutionary perspective, mammals and their ancestors have already undergone several hundred million years of natural selection favoring traits that could directly or indirectly favor increased longevity, and may thus have already settled on gene sequences that promote lifespan. Moreover, the very notion of a "life-extension factor" that could apply across taxa presumes a linear response rarely seen in biology."[21]
Much life extension research focuses on nutritiondiets or supplementsas a means to extend lifespan, although few of these have been systematically tested for significant longevity effects. The many diets promoted by anti-aging advocates are often contradictory.[original research?] A dietary pattern with some support from scientific research is caloric restriction.[22][23]
Preliminary studies of caloric restriction on humans using surrogate measurements have provided evidence that caloric restriction may have powerful protective effect against secondary aging in humans. Caloric restriction in humans may reduce the risk of developing Type 2 diabetes and atherosclerosis.[24]
The free-radical theory of aging suggests that antioxidant supplements, such as vitaminC, vitaminE, Q10, lipoic acid, carnosine, and N-acetylcysteine, might extend human life. However, combined evidence from several clinical trials suggest that -carotene supplements and high doses of vitaminE increase mortality rates.[25]Resveratrol is a sirtuin stimulant that has been shown to extend life in animal models, but the effect of resveratrol on lifespan in humans is unclear as of 2011.[26]
There are many traditional herbs purportedly used to extend the health-span, including a Chinese tea called Jiaogulan (Gynostemma pentaphyllum), dubbed "China's Immortality Herb."[27]Ayurveda, the traditional Indian system of medicine, describes a class of longevity herbs called rasayanas, including Bacopa monnieri, Ocimum sanctum, Curcuma longa, Centella asiatica, Phyllanthus emblica, Withania somnifera and many others.[27]
The anti-aging industry offers several hormone therapies. Some of these have been criticized for possible dangers to the patient and a lack of proven effect. For example, the American Medical Association has been critical of some anti-aging hormone therapies.[2]
Although some recent clinical studies have shown that low-dose growth hormone (GH) treatment for adults with GH deficiency changes the body composition by increasing muscle mass, decreasing fat mass, increasing bone density and muscle strength, improves cardiovascular parameters (i.e. decrease of LDL cholesterol), and affects the quality of life without significant side effects,[28][29][30] the evidence for use of growth hormone as an anti-aging therapy is mixed and based on animal studies. There are mixed reports that GH or IGF-1 signaling modulates the aging process in humans and about whether the direction of its effect is positive or negative.[31]
Some critics dispute the portrayal of aging as a disease. For example, Leonard Hayflick, who determined that fibroblasts are limited to around 50cell divisions, reasons that aging is an unavoidable consequence of entropy. Hayflick and fellow biogerontologists Jay Olshansky and Bruce Carnes have strongly criticized the anti-aging industry in response to what they see as unscrupulous profiteering from the sale of unproven anti-aging supplements.[4]
Politics relevant to the substances of life extension pertain mostly to communications and availability.[citation needed]
In the United States, product claims on food and drug labels are strictly regulated. The First Amendment (freedom of speech) protects third-party publishers' rights to distribute fact, opinion and speculation on life extension practices. Manufacturers and suppliers also provide informational publications, but because they market the substances, they are subject to monitoring and enforcement by the Federal Trade Commission (FTC), which polices claims by marketers. What constitutes the difference between truthful and false claims is hotly debated and is a central controversy in this arena.[citation needed]
Research by Sobh and Martin (2011) suggests that people buy anti-aging products to obtain a hoped-for self (e.g., keeping a youthful skin) or to avoid a feared-self (e.g., looking old). The research shows that when consumers pursue a hoped-for self, it is expectations of success that most strongly drive their motivation to use the product. The research also shows why doing badly when trying to avoid a feared self is more motivating than doing well. Interestingly, when product use is seen to fail it is more motivating than success when consumers seek to avoid a feared-self.[32]
The best-characterized anti-aging therapy was, and still is, CR. In some studies calorie restriction has been shown to extend the life of mice, yeast, and rhesus monkeys significantly.[33][34] However, a more recent study has shown that in contrast, calorie restriction has not improved the survival rate in rhesus monkeys.[35] Long-term human trials of CR are now being done. It is the hope of the anti-aging researchers that resveratrol, found in grapes, or pterostilbene, a more bio-available substance, found in blueberries, as well as rapamycin, a biotic substance discovered on Easter Island, may act as CR mimetics to increase the life span of humans.[36]
More recent work reveals that the effects long attributed to caloric restriction may be obtained by restriction of protein alone, and specifically of just the sulfur-containing amino acids cysteine and methionine.[37][38] Current research is into the metabolic pathways affected by variation in availability of products of these amino acids.
There are a number of chemicals intended to slow the aging process currently being studied in animal models.[39] One type of research is related to the observed effects a calorie restriction (CR) diet, which has been shown to extend lifespan in some animals[40] Based on that research, there have been attempts to develop drugs that will have the same effect on the aging process as a caloric restriction diet, which are known as Caloric restriction mimetic drugs. Some drugs that are already approved for other uses have been studied for possible longevity effects on laboratory animals because of a possible CR-mimic effect; they include rapamycin,[41]metformin and other geroprotectors.[42]MitoQ, Resveratrol and pterostilbene are dietary supplements that have also been studied in this context.[36][43][44]
Other attempts to create anti-aging drugs have taken different research paths. One notable direction of research has been research into the possibility of using the enzyme telomerase in order to counter the process of telomere shortening.[45] However, there are potential dangers in this, since some research has also linked telomerase to cancer and to tumor growth and formation.[46] In addition, some preparations, called senolytics are designed to effectively deplete senescent cells which poison an organism by their secretions.[47]
Future advances in nanomedicine could give rise to life extension through the repair of many processes thought to be responsible for aging. K. Eric Drexler, one of the founders of nanotechnology, postulated cell repair machines, including ones operating within cells and utilizing as yet hypothetical molecular computers, in his 1986 book Engines of Creation. Raymond Kurzweil, a futurist and transhumanist, stated in his book The Singularity Is Near that he believes that advanced medical nanorobotics could completely remedy the effects of aging by 2030.[48] According to Richard Feynman, it was his former graduate student and collaborator Albert Hibbs who originally suggested to him (circa 1959) the idea of a medical use for Feynman's theoretical micromachines (see nanotechnology). Hibbs suggested that certain repair machines might one day be reduced in size to the point that it would, in theory, be possible to (as Feynman put it) "swallow the doctor". The idea was incorporated into Feynman's 1959 essay There's Plenty of Room at the Bottom.[49]
Some life extensionists suggest that therapeutic cloning and stem cell research could one day provide a way to generate cells, body parts, or even entire bodies (generally referred to as reproductive cloning) that would be genetically identical to a prospective patient. Recently, the US Department of Defense initiated a program to research the possibility of growing human body parts on mice.[50] Complex biological structures, such as mammalian joints and limbs, have not yet been replicated. Dog and primate brain transplantation experiments were conducted in the mid-20th century but failed due to rejection and the inability to restore nerve connections. As of 2006, the implantation of bio-engineered bladders grown from patients' own cells has proven to be a viable treatment for bladder disease.[51] Proponents of body part replacement and cloning contend that the required biotechnologies are likely to appear earlier than other life-extension technologies.
The use of human stem cells, particularly embryonic stem cells, is controversial. Opponents' objections generally are based on interpretations of religious teachings or ethical considerations. Proponents of stem cell research point out that cells are routinely formed and destroyed in a variety of contexts. Use of stem cells taken from the umbilical cord or parts of the adult body may not provoke controversy.[52]
The controversies over cloning are similar, except general public opinion in most countries stands in opposition to reproductive cloning. Some proponents of therapeutic cloning predict the production of whole bodies, lacking consciousness, for eventual brain transplantation.
Replacement of biological (susceptible to diseases) organs with mechanical ones could extend life. This is the goal of 2045 Initiative.[53]
For cryonicists (advocates of cryopreservation), storing the body at low temperatures after death may provide an "ambulance" into a future in which advanced medical technologies may allow resuscitation and repair. They speculate cryogenic temperatures will minimize changes in biological tissue for many years, giving the medical community ample time to cure all disease, rejuvenate the aged and repair any damage that is caused by the cryopreservation process.
Many cryonicists do not believe that legal death is "real death" because stoppage of heartbeat and breathingthe usual medical criteria for legal deathoccur before biological death of cells and tissues of the body. Even at room temperature, cells may take hours to die and days to decompose. Although neurological damage occurs within 46 minutes of cardiac arrest, the irreversible neurodegenerative processes do not manifest for hours.[54] Cryonicists state that rapid cooling and cardio-pulmonary support applied immediately after certification of death can preserve cells and tissues for long-term preservation at cryogenic temperatures. People, particularly children, have survived up to an hour without heartbeat after submersion in ice water. In one case, full recovery was reported after 45 minutes underwater.[55] To facilitate rapid preservation of cells and tissue, cryonics "standby teams" are available to wait by the bedside of patients who are to be cryopreserved to apply cooling and cardio-pulmonary support as soon as possible after declaration of death.[56]
No mammal has been successfully cryopreserved and brought back to life, with the exception of frozen human embryos. Resuscitation of a postembryonic human from cryonics is not possible with current science. Some scientists still support the idea based on their expectations of the capabilities of future science.[57][58]
Another proposed life extension technology would combine existing and predicted future biochemical and genetic techniques. SENS proposes that rejuvenation may be obtained by removing aging damage via the use of stem cells and tissue engineering, telomere-lengthening machinery, allotopic expression of mitochondrial proteins, targeted ablation of cells, immunotherapeutic clearance, and novel lysosomal hydrolases.[59]
While many biogerontologists find these ideas "worthy of discussion"[60][61] and SENS conferences feature important research in the field,[62][63] some contend that the alleged benefits are too speculative given the current state of technology, referring to it as "fantasy rather than science".[3][5]
Gene therapy, in which nucleic acid polymers are delivered as a drug and are either expressed as proteins, interfere with the expression of proteins, or correct genetic mutations, has been proposed as a future strategy to prevent aging.[64][65]
A large array of genetic modifications have been found to increase lifespan in model organisms such as yeast, nematode worms, fruit flies, and mice. As of 2013, the longest extension of life caused by a single gene manipulation was roughly 150% in mice and 10-fold in nematode worms.[66]
In The Selfish Gene, Richard Dawkins describes an approach to life-extension that involves "fooling genes" into thinking the body is young.[67] Dawkins attributes inspiration for this idea to Peter Medawar. The basic idea is that our bodies are composed of genes that activate throughout our lifetimes, some when we are young and others when we are older. Presumably, these genes are activated by environmental factors, and the changes caused by these genes activating can be lethal. It is a statistical certainty that we possess more lethal genes that activate in later life than in early life. Therefore, to extend life, we should be able to prevent these genes from switching on, and we should be able to do so by "identifying changes in the internal chemical environment of a body that take place during aging... and by simulating the superficial chemical properties of a young body".[68]
According to some lines of thinking, the ageing process is routed into a basic reduction of biological complexity,[69] and thus loss of information. In order to reverse this loss, gerontologist Marios Kyriazis suggested that it is necessary to increase input of actionable and meaningful information both individually (into individual brains),[70] and collectively (into societal systems).[71] This technique enhances overall biological function through up-regulation of immune, hormonal, antioxidant and other parameters, resulting in improved age-repair mechanisms. Working in parallel with natural evolutionary mechanisms that can facilitate survival through increased fitness, Kryiazis claims that the technique may lead to a reduction of the rate of death as a function of age, i.e. indefinite lifespan.[72]
One hypothetical future strategy that, as some suggest, "eliminates" the complications related to a physical body, involves the copying or transferring (e.g. by progressively replacing neurons with transistors) of a conscious mind from a biological brain to a non-biological computer system or computational device. The basic idea is to scan the structure of a particular brain in detail, and then construct a software model of it that is so faithful to the original that, when run on appropriate hardware, it will behave in essentially the same way as the original brain.[73] Whether or not an exact copy of one's mind constitutes actual life extension is matter of debate.
The extension of life has been a desire of humanity and a mainstay motif in the history of scientific pursuits and ideas throughout history, from the Sumerian Epic of Gilgamesh and the Egyptian Smith medical papyrus, all the way through the Taoists, Ayurveda practitioners, alchemists, hygienists such as Luigi Cornaro, Johann Cohausen and Christoph Wilhelm Hufeland, and philosophers such as Francis Bacon, Ren Descartes, Benjamin Franklin and Nicolas Condorcet. However, the beginning of the modern period in this endeavor can be traced to the end of the 19th beginning of the 20th century, to the so-called fin-de-sicle (end of the century) period, denoted as an end of an epoch and characterized by the rise of scientific optimism and therapeutic activism, entailing the pursuit of life extension (or life-extensionism). Among the foremost researchers of life extension at this period were the Nobel Prize winning biologist Elie Metchnikoff (1845-1916) -- the author of the cell theory of immunity and vice director of Institut Pasteur in Paris, and Charles-douard Brown-Squard (1817-1894) -- the president of the French Biological Society and one of the founders of modern endocrinology.[74]
Sociologist James Hughes claims that science has been tied to a cultural narrative of conquering death since the Age of Enlightenment. He cites Francis Bacon (15611626) as an advocate of using science and reason to extend human life, noting Bacon's novel New Atlantis, wherein scientists worked toward delaying aging and prolonging life. Robert Boyle (16271691), founding member of the Royal Society, also hoped that science would make substantial progress with life extension, according to Hughes, and proposed such experiments as "to replace the blood of the old with the blood of the young". Biologist Alexis Carrel (18731944) was inspired by a belief in indefinite human lifespan that he developed after experimenting with cells, says Hughes.[75]
In 1970, the American Aging Association was formed under the impetus of Denham Harman, originator of the free radical theory of aging. Harman wanted an organization of biogerontologists that was devoted to research and to the sharing of information among scientists interested in extending human lifespan.
In 1976, futurists Joel Kurtzman and Philip Gordon wrote No More Dying. The Conquest Of Aging And The Extension Of Human Life, (ISBN 0-440-36247-4) the first popular book on research to extend human lifespan. Subsequently, Kurtzman was invited to testify before the House Select Committee on Aging, chaired by Claude Pepper of Florida, to discuss the impact of life extension on the Social Security system.
Saul Kent published The Life Extension Revolution (ISBN 0-688-03580-9) in 1980 and created a nutraceutical firm called the Life Extension Foundation, a non-profit organization that promotes dietary supplements. The Life Extension Foundation publishes a periodical called Life Extension Magazine. The 1982 bestselling book Life Extension: A Practical Scientific Approach (ISBN 0-446-51229-X) by Durk Pearson and Sandy Shaw further popularized the phrase "life extension".
In 1983, Roy Walford, a life-extensionist and gerontologist, published a popular book called Maximum Lifespan. In 1988, Walford and his student Richard Weindruch summarized their research into the ability of calorie restriction to extend the lifespan of rodents in The Retardation of Aging and Disease by Dietary Restriction (ISBN 0-398-05496-7). It had been known since the work of Clive McCay in the 1930s that calorie restriction can extend the maximum lifespan of rodents. But it was the work of Walford and Weindruch that gave detailed scientific grounding to that knowledge.[citation needed] Walford's personal interest in life extension motivated his scientific work and he practiced calorie restriction himself. Walford died at the age of 80 from complications caused by amyotrophic lateral sclerosis.
Money generated by the non-profit Life Extension Foundation allowed Saul Kent to finance the Alcor Life Extension Foundation, the world's largest cryonics organization. The cryonics movement had been launched in 1962 by Robert Ettinger's book, The Prospect of Immortality. In the 1960s, Saul Kent had been a co-founder of the Cryonics Society of New York. Alcor gained national prominence when baseball star Ted Williams was cryonically preserved by Alcor in 2002 and a family dispute arose as to whether Williams had really wanted to be cryopreserved.
Regulatory and legal struggles between the Food and Drug Administration (FDA) and the Life Extension Foundation included seizure of merchandise and court action. In 1991, Saul Kent and Bill Faloon, the principals of the Foundation, were jailed. The LEF accused the FDA of perpetrating a "Holocaust" and "seeking gestapo-like power" through its regulation of drugs and marketing claims.[76]
In 2003, Doubleday published "The Immortal Cell: One Scientist's Quest to Solve the Mystery of Human Aging," by Michael D. West. West emphasised the potential role of embryonic stem cells in life extension.[77]
Other modern life extensionists include writer Gennady Stolyarov, who insists that death is "the enemy of us all, to be fought with medicine, science, and technology";[78]transhumanist philosopher Zoltan Istvan, who proposes that the "transhumanist must safeguard one's own existence above all else";[79] futurist George Dvorsky, who considers aging to be a problem that desperately needs to be solved;[80] and recording artist Steve Aoki, who has been called "one of the most prolific campaigners for life extension".[81]
In 1991, the American Academy of Anti-Aging Medicine (A4M) was formed as a non-profit organization to create what it considered an anti-aging medical specialty distinct from geriatrics, and to hold trade shows for physicians interested in anti-aging medicine. The A4M trains doctors in anti-aging medicine and publicly promotes the field of anti-aging research. It has about 26,000 members, of whom about 97% are doctors and scientists.[82] The American Board of Medical Specialties recognizes neither anti-aging medicine nor the A4M's professional standing.[83]
In 2003, Aubrey de Grey and David Gobel formed the Methuselah Foundation, which gives financial grants to anti-aging research projects. In 2009, de Grey and several others founded the SENS Research Foundation, a California-based scientific research organization which conducts research into aging and funds other anti-aging research projects at various universities.[84] In 2013, Google announced Calico, a new company based in San Francisco that will harness new technologies to increase scientific understanding of the biology of aging.[85] It is led by Arthur D. Levinson,[86] and its research team includes scientists such as Hal V. Barron, David Botstein, and Cynthia Kenyon. In 2014, biologist Craig Venter founded Human Longevity Inc., a company dedicated to scientific research to end aging through genomics and cell therapy. They received funding with the goal of compiling a comprehensive human genotype, microbiome, and phenotype database.[87]
Aside from private initiatives, aging research is being conducted in university laboratories, and includes universities such as Harvard and UCLA. University researchers have made a number of breakthroughs in extending the lives of mice and insects by reversing certain aspects of aging.[88][89][90][91]
Though many scientists state[92] that life extension and radical life extension are possible, there are still no international or national programs focused on radical life extension. There are political forces staying for and against life extension. By 2012, in Russia, the United States, Israel, and the Netherlands, the Longevity political parties started. They aimed to provide political support to radical life extension research and technologies, and ensure the fastest possible and at the same time soft transition of society to the next step life without aging and with radical life extension, and to provide access to such technologies to most currently living people.[93]
Leon Kass (chairman of the US President's Council on Bioethics from 2001 to 2005) has questioned whether potential exacerbation of overpopulation problems would make life extension unethical.[94] He states his opposition to life extension with the words:
"simply to covet a prolonged life span for ourselves is both a sign and a cause of our failure to open ourselves to procreation and to any higher purpose ... [The] desire to prolong youthfulness is not only a childish desire to eat one's life and keep it; it is also an expression of a childish and narcissistic wish incompatible with devotion to posterity."[95]
John Harris, former editor-in-chief of the Journal of Medical Ethics, argues that as long as life is worth living, according to the person himself, we have a powerful moral imperative to save the life and thus to develop and offer life extension therapies to those who want them.[96]
Transhumanist philosopher Nick Bostrom has argued that any technological advances in life extension must be equitably distributed and not restricted to a privileged few.[97] In an extended metaphor entitled "The Fable of the Dragon-Tyrant", Bostrom envisions death as a monstrous dragon who demands human sacrifices. In the fable, after a lengthy debate between those who believe the dragon is a fact of life and those who believe the dragon can and should be destroyed, the dragon is finally killed. Bostrom argues that political inaction allowed many preventable human deaths to occur.[98]
Life extension is a controversial topic due to fear of overpopulation and possible effects on society.[99] Biogerontologist Aubrey De Grey counters the overpopulation critique by pointing out that the therapy could postpone or eliminate menopause, allowing women to space out their pregnancies over more years and thus decreasing the yearly population growth rate.[100] Moreover, the philosopher and futurist Max More argues that, given the fact the worldwide population growth rate is slowing down and is projected to eventually stabilize and begin falling, superlongevity would be unlikely to contribute to overpopulation.[99]
A Spring 2013 Pew Research poll in the United States found that 38% of Americans would want life extension treatments, and 56% would reject it. However, it also found that 68% believed most people would want it and that only 4% consider an "ideal lifespan" to be more than 120 years. The median "ideal lifespan" was 91 years of age and the majority of the public (63%) viewed medical advances aimed at prolonging life as generally good. 41% of Americans believed that radical life extension (RLE) would be good for society, while 51% said they believed it would be bad for society.[101] One possibility for why 56% of Americans claim they would reject life extension treatments may be due to the cultural perception that living longer would result in a longer period of decrepitude, and that the elderly in our current society are unhealthy.[102]
Religious people are no more likely to oppose life extension than the unaffiliated,[101] though some variation exists between religious denominations.
Most mainstream medical organizations and practitioners do not consider aging to be a disease. David Sinclair says: "Idon't see aging as a disease, but as a collection of quite predictable diseases caused by the deterioration of the body".[103] The two main arguments used are that aging is both inevitable and universal while diseases are not.[104] However, not everyone agrees. Harry R. Moody, Director of Academic Affairs for AARP, notes that what is normal and what is disease strongly depends on a historical context.[105] David Gems, Assistant Director of the Institute of Healthy Ageing, strongly argues that aging should be viewed as a disease.[106] In response to the universality of aging, David Gems notes that it is as misleading as arguing that Basenji are not dogs because they do not bark.[107] Because of the universality of aging he calls it a 'special sort of disease'. Robert M. Perlman, coined the terms aging syndrome and disease complex in 1954 to describe aging.[108]
The discussion whether aging should be viewed as a disease or not has important implications. It would stimulate pharmaceutical companies to develop life extension therapies and in the United States of America, it would also increase the regulation of the anti-aging market by the FDA. Anti-aging now falls under the regulations for cosmetic medicine which are less tight than those for drugs.[107][109]
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Zeitgeist (film series) – Wikipedia
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Zeitgeist: The Movie Directed by Peter Joseph Produced by Peter Joseph Written by Peter Joseph Music by Peter Joseph Edited by Peter Joseph Distributed by GMP LLC
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Zeitgeist: The Movie is a 2007 film by Peter Joseph presenting a number of conspiracy theories.[3] The film assembles archival footage, animations and narration.[4] Released online on June 18, 2007, it soon received tens of millions of views on Google Video, YouTube, and Vimeo.[5] According to Peter Joseph, the original Zeitgeist was not presented in a film format, but was a "performance piece consisting of a vaudevillian, multimedia style event using recorded music, live instruments, and video".[5]
The film's introduction features animations, footage of war, explosions, and the September 11 attacks and audio quotes from Chgyam Trungpa Rinpoche and George Carlin. The rest of the film is in three parts narrated by Peter Joseph.[6]
Part I asserts that the Christian religion is mainly derived from other religions, astronomical assertions, astrological myths, and other traditions. In furtherance of the Jesus myth hypothesis, this part disputes the historicity of Jesus, who, it claims, is a literary and astrological hybrid, nurtured by political forces and opportunists.[6]
Part II alleges that the 9/11 attacks were either orchestrated or allowed to happen by elements within the United States government in order to generate mass fear, justify the War on Terror, provide a pretext for the curtailment of civil liberties, and produce economic gain. It asserts that the U.S. government had advance knowledge of the attacks, that the military deliberately allowed the planes to reach their targets, and that World Trade Center buildings 1, 2, and 7 underwent a controlled demolition.[6]
Part III states that the Federal Reserve System is controlled by a small cabal of international bankers who conspire to create global calamities to enrich themselves.[4] Three wars involving the United States during the twentieth century are highlighted as part of this alleged agenda, started by specifically engineered events, including the sinking of the RMS Lusitania, the attack on Pearl Harbor, and the Gulf of Tonkin Incident. The film asserts that such wars serve to sustain conflict in general and force the U.S. government to borrow money, thereby increasing the profits of the international bankers. The film also claims that the Federal Income Tax is illegal.[6]
Part III also alleges a secret agreement to merge the United States, Canada and Mexico into a North American Union as a step toward the creation of a single world government. The film speculates that under such a government, every human could be implanted with an RFID chip to monitor individual activity and suppress dissent.
The first film received almost universal condemnation from the media, though it also "attracted massive interest" from the public.[5][7]
The newspaper The Arizona Republic described Zeitgeist: The Movie as "a bramble of conspiracy theories involving Sept. 11, the international monetary system, and Christianity" saying also that the movie trailer states that "there are people guiding your life and you don't even know it".[8]
A review in The Irish Times wrote that "these are surreal perversions of genuine issues and debates, and they tarnish all criticism of faith, the Bush administration, and globalizationthere are more than enough factual injustices in this world to be going around without having to invent fictional ones".[7]
Ivor Tossell in the Globe and Mail cited it as an example of how modern conspiracy theories are promulgated, though he praised its effectiveness:
"The film is an interesting object lesson on how conspiracy theories get to be so popular.... It's a driven, if uneven, piece of propaganda, a marvel of tight editing and fuzzy thinking. Its on-camera sources are mostly conspiracy theorists, co-mingled with selective eyewitness accounts, drawn from archival footage and often taken out of context. It derides the media as a pawn of the International Bankers, but produces media reports for credibility when convenient. The film ignores expert opinion, except the handful of experts who agree with it. And yet, it's compelling. It shamelessly ploughs forward, connecting dots with an earnest certainty that makes you want to give it an A for effort."[4]
Filipe Feio, reflecting upon the film's Internet popularity in Dirio de Notcias, stated that "[f]iction or not, Zeitgeist: The Movie threatens to become the champion of conspiracy theories of today".[9]
Michael Shermer, founder of the Skeptics Society, mentioned Zeitgeist in an article in Scientific American on skepticism in the age of mass media and the postmodern belief in the relativism of truth. He argues that this belief, coupled with a "clicker culture of mass media," results in a multitude of various truth claims packaged in "infotainment units", in the form of films such as Zeitgeist and Loose Change.[10]
Jane Chapman, a film producer and reader in media studies at the University of Lincoln, called Zeitgeist "a fast-paced assemblage of agitprop," an example of "unethical film-making".[11] She accused Peter Joseph of "implicit deception" through the use of standard film-making propaganda techniques. While parts of the film are, she says, "comically" self-defeating, the nature of "twisted evidence" and use of Madrid bomb footage to imply it is of the London bombings amount to "ethical abuse in sourcing". She finishes her analysis with the comment: "Thus, legitimate questions about what happened on 9/11, and about corruption in religious and financial organizations, are all undermined by the film's determined effort to maximize an emotional response at the expense of reasoned argument."
Alex Jones, American radio host, conspiracy theorist and executive producer of Loose Change, stated that film segments of Zeitgeist are taken directly from his documentary Terrorstorm, and that he supports "90 percent" of the film.[12]
Skeptic magazine's Tim Callahan, criticizing the parts of the film on the origins of Christianity, wrote that "some of what it asserts is true. Unfortunately, this material is liberallyand sloppilymixed with material that is only partially true and much that is plainly and simply bogus."[13]
Chris Forbes, Senior lecturer in Ancient History of Macquarie University and member of the Synod of the Diocese of Sydney, severely criticized Part I of the film, stating that it has no basis in serious scholarship or ancient sources, and that it relies on amateur sources that recycle frivolous ideas from one another, commenting that "[i]t is extraordinary how many claims it makes which are simply not true".[14] Similar conclusions were reached by Dr. Mark Foreman of Liberty University.[15]
Paul Constant writing in Seattle newspaper The Stranger characterized the film as "fiction couched in a few facts".[6] Of the religious critique in the film he said: "First the film destroys the idea of God, and then, through the lens of 9/11, it introduces a sort of new Bizarro God. Instead of an omnipotent, omniscient being who loves you and has inspired a variety of organized religions, there is an omnipotent, omniscient organization of ruthless beings who hate you and want to take your rights away, if not throw you in a work camp forever."[6] Adding "it's probably drawing more people into the Truth movement than anything else".[6]
In Tablet Magazine, journalist Michelle Goldberg criticized Zeitgeist: The Movie as being "steeped in far-right, isolationist, and covertly anti-Semitic conspiracy theories," claiming that the film borrowed from the work of Eustace Mullins, Lyndon LaRouche, and radio host Alex Jones, and that it portrays a cabal of international bankers purportedly ruling the world.[5] In an interview with TheMarker, Joseph said that while the film does mention bankers it does not seek to blame any individual or group of individuals. He argued they are merely a product of a socioeconomic system in need of change.[16]
Chip Berlet wrote that the 9/11 conspiracy theories "are bait used to attract viewers from the 9/11 truth movement and others who embrace conspiracist thinking to the idiosyncratic antireligion views of the videographer and the world of right-wing antisemitic theories of a global banking conspiracy".[17]
Jay Kinney questioned the accuracy of its claims and the quality of its arguments, describing it as agitprop and propaganda.[18] At times, according to Kinney, "Zeitgeist engages in willful confusion by showing TV screen shots of network or cable news with voice-overs from unidentified people not associated with the news programs. If one weren't paying close attention, the effect would be to confer the status and authority of TV news upon the words being spoken. Even when quotes or sound bites are attributed to a source, there's no way to tell if they are quoted correctly or in context."[18]
In June 2013, Peter Joseph directed the music video for "God Is Dead?" by Black Sabbath, using extensive imagery from Zeitgeist: The Movie and its sequels.[19]
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Zeitgeist: Addendum is a 2008 film produced and directed by Peter Joseph, and is a sequel to the 2007 film, Zeitgeist: The Movie. It premiered at the 5th Annual Artivist Film Festival in Los Angeles, California on October 2, 2008.[citation needed]
The film begins and ends with excerpts from a speech by Jiddu Krishnamurti. The remainder of the film is narrated by Peter Joseph and divided into four parts, which are prefaced by on-screen quotations from Krishnamurti, John Adams, Bernard Lietaer, and Thomas Paine, respectively.
Part I covers the process of fractional-reserve banking as illustrated in Modern Money Mechanics, by the Federal Reserve Bank of Chicago. The film suggests that society is manipulated into economic slavery through debt-based monetary policies by requiring individuals to submit for employment in order to pay off their debt.
Part II has an interview with John Perkins, author of Confessions of an Economic Hitman, who says he was involved in the subjugation of Latin American economies by multinational corporations and the United States government, including involvement in the overthrow of Latin American heads-of-state. Perkins sees the US as a corporatocracy, in which maximization of profits is the first priority.
Part III introduces futurist Jacque Fresco and The Venus Project and asserts a need to move away from current socioeconomic paradigms. Fresco states that capitalism perpetuates the conditions it claims to address, as problems are only solved if there is money to be made. The film looks at Fresco's proposal of a resource-based economy, which puts environmental friendliness, sustainability and abundance as fundamental societal goals. He goes on to discuss technology which he sees as the primary driver of human advancement, and he describes politics as being unable to solve any problems.
Part IV suggests that the primary reason for what the film sees as society's social values ("warfare, corruption, oppressive laws, social stratification, irrelevant superstitions, environmental destruction, and a despotic, socially indifferent, profit oriented ruling class") is a collective ignorance of "the emergent and symbiotic aspects of natural law". The film advocates the following actions for achieving social change: boycotting of the most powerful banks in the Federal Reserve System, the major news networks, the military, energy corporations, all political systems; and joining, and supporting The Zeitgeist Movement.
Zeitgeist: Addendum won the 2008 Artivist Film Festival's award for best feature ("Artivist Spirit" category).[20]
Originally, the film was uploaded-released on Google video. The current video posting on YouTube surpassed 5,000,000 views by late 2013.[21]
Alan Feuer of The New York Times noted that while the first film was famous for alleging that the attacks of September 11 were an inside job, the second, "was all but empty of such conspiratorial notions, directing its rhetoric and high production values toward posing a replacement for the evils of the banking system and a perilous economy of scarcity and debt".[22]
Zeitgeist: Moving Forward is the third installment in Peter Joseph's Zeitgeist film series. The film premiered at the JACC Theater in Los Angeles on January 15, 2011 at the Artivist Film Festival,[23] was released in theaters and online. As of November 2014, the film has over 23 million views on YouTube.[24] The film is arranged into four parts. Each part contains interviews, narration and animated sequences.[25]
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The film begins with an animated sequence narrated by Jacque Fresco. He describes his adolescent life and his discontinuation of public education at the age of 14 and describes his early life influences.
Part I: Human Nature
Human behavior and the nature vs. nurture debate is discussed, which Robert Sapolsky refers to as a "false dichotomy." Disease, criminal activity, and addictions are also discussed. The overall conclusion of Part I is that social environment and cultural conditioning play a large part in shaping human behavior.
Part II: Social Pathology
John Locke and Adam Smith are discussed in regard to modern economics. The film critically questions the economic need for private property, money, and the inherent inequality between agents in the system. Also seen critically is the need for cyclical consumption in order to maintain market share, resulting in wasted resources and planned obsolescence. According to the movie, the current monetary system will result in default or hyperinflation at some future time.
Part III: Project Earth
As with Zeitgeist: Addendum, the film presents a "resource-based economy" as advocated by Jacque Fresco discussing how human civilization could start from a new beginning in relation to resource types, locations, quantities, to satisfy human demands; track the consumption and depletion of resources to regulate human demands and maintain the condition of the environment.
Part IV: Rise
The current worldwide situation is described as disastrous. A case is presented that pollution, deforestation, climate change, overpopulation, and warfare are all created and perpetuated by the socioeconomic system. Various poverty statistics are shown that suggest a progressive worsening of world culture.
The final scene of the film shows a partial view of earth from space, followed by a sequence of superimposed statements; "This is your world", "This is our world", and "The revolution is now".
List of Interviewees
Zeitgeist: Moving Forward received "Best Political Documentary" in 2011 from the Action on Film International Film Festival.[26]
A The Socialist Standard review said the film's use of animation and humour gave it a "well rounded feel", though it criticized the "shaky economic analysis" in the second part of the film, saying "Karl Marx had already undertaken a more scientific analysis", adding, "the analysis is at least on the right track". Regarding transition to the new system proposed in the film, the reviewer noted "there is no mention of how to get from here to there".[27]
In an article, in Tablet Magazine, Michelle Goldberg described the film as "silly enough that at times [she] suspected it was [a] sly satire about new-age techno-utopianism instead of an example of it".[5] She describes the 3 Zeitgeist movies as "a series of 3 apocalyptic cult documentaries.[5]
Zeitgeist: The Movie (2007) started the chain of events leading to the formation of the Zeitgeist movement.[5] The group advocates transition from the global money-based economic system to a post-scarcity economy or resource-based economy. VC Reporter's Shane Cohn summarized the movement's charter as: "Our greatest social problems are the direct results of our economic system".[28] Joseph created a political movement that, according to The Daily Telegraph, dismisses historic religious concepts as misleading and embraces a version of sustainable ecological concepts and scientific administration of society.[29] The group describes the current socioeconomic system as structurally corrupt and inefficient in the use of resources.[22][30]Michelle Goldberg described the Zeitgeist movement as "the first Internet-based apocalyptic cult".[5]
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Basic Income Guarantee – Your Right to Economic Security …
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"This book is a great idea - brilliantly stated. Some may think it's ultra-liberal, as they did when I proposed a similar idea in 1972. I see it as true conservatism - the right of income for all Americans sufficient for food, shelter, and basic necessities. Or, what Jefferson referred to as life, liberty, and the pursuit of happiness." - U.S. Senator George McGovern, 1972 Democratic Party Presidential Candidate
"Sheahen and I are as far apart on political philosophy and the causes of the nation's current mess as two people can be, but we both think that a basic income guarantee has to be part of the solution. That says something about the potential of this important idea whose time, as we both hope, is coming. Basic Income Guarantee will help make that happen." - Charles Murray, author of In Our Hands: A Plan to Replace the Welfare State
"Basic Income Guarantee is a fascinating, lucid presentation of a complex subject. Sheahen asks and answers the questions of what a just society should and could do to overcome income insecurity. Given our prolonged economic malaise, everyone in America should be thinking about it." - Theresa Funiciello, author of Tyranny of Kindness and head of Social Agenda
"Absent as an issue for almost fifty years, Allan Sheahen places the idea of a basic income for all Americans squarely back on the national agenda. In plain English, this radical idea is not only clearly explained but answers even the toughest objections that can be raised. This book should make sense even to my most dysfunctional colleagues in Congress." - Bob Filner, U.S. Congressman of San Diego and former chairman of the House Veterans Affairs Committee
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Basic Income Guarantee - Your Right to Economic Security ...
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Modern Satanism: Anatomy of a Radical Subculture by Chris …
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In 1966, Anton LaVey introduced to the world the Church of Satan, an atheistic religion devoted to the philosophy of individualism and pitilessness often associated with Satan. Modern Satanism offers a comprehensive survey and analysis of the church that LaVey built. Satanism has been an open religion for forty years now and operates successfully in its self-created countercultural niche. Given the provocative nature of its name, contemporary Satanism is only superficially understood as an alternative religion/ideology, and all-too-frequently seen as a medieval superstition and associated with rumors of obscure rituals, perverse hedonism, cult-like behavior, and tales of ritual abuse and murder. These may be misconceptions, but the truth behind the unenviable reputation is no less dramatic. Satanism generally eschews supernatural beliefs and embodies a staunchly individualistic, pitiless, anti-egalitarian creed. If there is anything fundamentally diabolical about modern Satanism, it stems more from the echoes of Nazism in its theories than from its horror-comic trappings.Modern Satanism covers the history, ideology, personalities, and practices of the decentralized international movement that contemporary Satanism has become. The work addresses the various beliefs and practices espoused by those who follow it: the ideal of Satan as a rebellious emblem; Satanism's occult, literary, and philosophical influences; the history of the Church of Satan and other Satanic organizations; the ideology of Satanism; Satanism's frequent flirtations and strong parallels with neo-Nazism and other forms of extremism; Satanism in the media and popular culture; and the reasons for Satanism's continuing attractiveness to new converts. Though the tone of the work attempts to remain neutral when discussing historical matters, it is by necessity critical of the subculture's extremist rhetoric and recurring associations with the far right and racialist extremism.
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Introduction: Counter the Counterculture
1. The Morning Star
2. Baleful Eyes
3. The Black Pope
4. Man, the Animal
5. Satanic Legions
6. The Left Hand Path
7. In The Company of Killers
8. The Plague of Nazism
9. Natural Born Satanists
10. Apocalypse Cheerleaders
Conclusion: Worst Case Scenario
Notes
Bibliography
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Modern Satanism: Anatomy of a Radical Subculture by Chris ...
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NATO phonetic alphabet – Wikipedia
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The International Radiotelephony Spelling Alphabet, commonly known as the ICAO phonetic alphabet, sometimes called the NATO alphabet or spelling alphabet and the ITU radiotelephonic or phonetic alphabet, is the most widely used radiotelephonic spelling alphabet. Although often called "phonetic alphabets", spelling alphabets are not associated with phonetic transcription systems such as the International Phonetic Alphabet. Instead, the International Civil Aviation Organization (ICAO) alphabet assigned codewords acrophonically to the letters of the English alphabet, so that critical combinations of letters and numbers can be pronounced and understood by those who exchange voice messages by radio or telephone regardless of language barriers or the quality of the communication channel.[1]
The 26 code words in the NATO phonetic alphabet are assigned to the 26 letters of the English alphabet in alphabetical order as follows: Alfa, Bravo, Charlie, Delta, Echo, Foxtrot, Golf, Hotel, India, Juliett, Kilo, Lima, Mike, November, Oscar, Papa, Quebec, Romeo, Sierra, Tango, Uniform, Victor, Whiskey, X-ray, Yankee, Zulu.
After the phonetic alphabet was developed by the International Civil Aviation Organization (ICAO)[2] (see history below) it was adopted by many other international and national organizations, including the North Atlantic Treaty Organization (NATO), the International Telecommunication Union (ITU), the International Maritime Organization (IMO), the American Federal Aviation Administration (FAA), the Alliance for Telecommunications Industry Solutions (ATIS), and the International Amateur Radio Union (IARU).
It is a subset of the much older International Code of Signals (INTERCO), which originally included visual signals by flags or flashing light, sound signals by whistle, siren, foghorn, or bell, as well as one, two, or three letter codes for many phrases.[3] The same alphabetic code words are used by all agencies, but each agency chooses one of two different sets of numeric code words. NATO uses the regular English numeric words (Zero, One, with some alternative pronunciations), whereas the IMO provides for compound numeric words (Nadazero, Unaone, Bissotwo...). In practice these are used very rarely, as they frequently result in confusion between speakers of different languages.
An alternative name for the ICAO spelling alphabet, "NATO phonetic alphabet," exists because it appears in Allied Tactical Publication ATP-1, Volume II: Allied Maritime Signal and Maneuvering Book used by all allied navies of NATO, which adopted a modified form of the International Code of Signals. Because the latter allows messages to be spelled via flags or Morse code, it naturally named the code words used to spell out messages by voice its "phonetic alphabet". The name NATO phonetic alphabet became widespread because the signals used to facilitate the naval communications and tactics of NATO have become global.[4] However, ATP-1 is marked NATO Confidential (or the lower NATO Restricted) so it is not available publicly. Nevertheless, a NATO unclassified version of the document is provided to foreign, even hostile, militaries, even though they are not allowed to make it available publicly. The spelling alphabet is now also defined in other unclassified international military documents.[5] The NATO alphabet appeared in some United States Air Force Europe publications during the Cold War. A particular example was the Ramstein Air Base, Telephone Directory published between 1969 and 1973 (currently out of print). The American and NATO versions had differences and the translation was provided as a convenience. Differences included Alfa, Bravo and Able, Baker for the first two letters.
The ICAO developed this system in the 1950s in order to account for discrepancies that might arise in communications as a result of multiple alphabet naming systems coexisting in different places and organizations.[6]
In the official[7] version of the alphabet, the non-English spellings Alfa and Juliett are used. Alfa is spelled with an f as it is in most European languages because the English and French spelling alpha would not be pronounced properly by native speakers of some other languages who may not know that ph should be pronounced as f. Juliett is spelled with a tt for French speakers, because they may otherwise treat a single final t as silent. In some English versions of the alphabet, one or both of these may have their standard English spelling.[8]
The final choice of code words for the letters of the alphabet and for the digits was made after hundreds of thousands of comprehension tests involving 31 nationalities. The qualifying feature was the likelihood of a code word being understood in the context of others. For example, football has a higher chance of being understood than foxtrot in isolation, but foxtrot is superior in extended communication.[9]
The pronunciation of the code words varies according to the language habits of the speaker. To eliminate wide variations in pronunciation, recordings and posters illustrating the pronunciation desired by the ICAO are available.[9][10] However, there are still differences in pronunciation between the ICAO and other agencies, and the ICAO has conflicting Roman-alphabet and IPA transcriptions. Also, although all codes for the letters of the alphabet are English words, they are not in general given English pronunciations. Assuming that the transcriptions are not intended to be precise, only 11 of the 26Bravo, Echo, Hotel, Juliet(t), Kilo, Mike, Papa, Quebec, Romeo, Whiskey, and Zuluare given English pronunciations by all these agencies, though not always the same English pronunciations.
Pronunciations are somewhat uncertain because the agencies, while ostensibly using the same pronunciations, give different transcriptions, which are often inconsistent from letter to letter. The ICAO gives different pronunciations in IPA transcription than in respelling, and the FAA also gives different pronunciations depending on the publication consulted, the FAA Aeronautical Information Manual (4-2-7), the FAA Flight Services manual (14.1.5), or the ATC manual (2-4-16). ATIS gives English spellings, but does not give pronunciations or numbers. The ICAO, NATO, and FAA use modifications of English numerals, with stress on one syllable, while the ITU and IMO compound pseudo-Latinate numerals with a slightly different set of modified English numerals, and with stress on each syllable. Numbers 1099 are spelled out (that is, 17 is "17" and 60 is "60"), while for hundreds and thousands the English words hundred and thousand are used.[8][10][12][13][14][22]
The pronunciation of the digits 3, 4, 5, and 9 differs from standard English being pronounced tree, fower, fife, and niner. The digit 3 is specified as tree so that it is not pronounced sri; the long pronunciation of 4 (still found in some English dialects) keeps it somewhat distinct from for; 5 is pronounced with a second "f" because the normal pronunciation with a "v" is easily confused with "fire" (a command to shoot); and 9 has an extra syllable to keep it distinct from German nein 'no'.
Only the ICAO prescribes pronunciation with the IPA, and then only for letters.[10] Several of the pronunciations indicated are slightly modified from their normal English pronunciations: /lf, brvo, li, delt, fkstrt, lf, lim, sk, sier, tno, unifrm, vikt, jnki/, partially due to the substitution of final schwas with the ah vowel; in addition, the intended distinction between the short vowels /o / and the long vowels /o / is obscure, and has been ignored in the consolidated transcription above. Both the IPA and respelled pronunciations were developed by the ICAO before 1956 with advice from the governments of both the United States and United Kingdom,[23] so the pronunciations of both General American English and British Received Pronunciation are evident, especially in the rhotic and non-rhotic accents. The respelled version is usually at least consistent with a rhotic accent ('r' pronounced), as in CHAR LEE, SHAR LEE, NO VEM BER, YOU NEE FORM, and OO NEE FORM, whereas the IPA version usually specifies a non-rhotic accent ('r' pronounced only before a vowel), as in tli, li, novemb, and junifm. Exceptions are OSS CAH, VIK TAH and unifrm. The IPA form of Golf implies it is pronounced gulf, which is not either General American English or British Received Pronunciation. Different agencies assign different stress patterns to Bravo, Hotel, Juliett, November, Papa, X-ray; the ICAO has different stresses for Bravo, Juliett, X-ray in its respelled and IPA transcriptions. The mid back [] vowel transcribed in Oscar and Foxtrot is actually a low vowel in both Received British and General American, and has been interpreted as such above. Furthermore, the pronunciation prescribed for "whiskey" has no initial [h], although some speakers in both General American and RP pronounce an h here, and an initial [h] is categorical in Scotland and Ireland.
The first internationally recognized spelling alphabet was adopted by the ITU during 1927. The experience gained with that alphabet resulted in several changes being made during 1932 by the ITU. The resulting alphabet was adopted by the International Commission for Air Navigation, the predecessor of the ICAO, and was used for civil aviation until World War II.[23] It continued to be used by the IMO until 1965:
Amsterdam, Baltimore, Casablanca, Denmark, Edison, Florida, Gallipoli, Havana, Italia, Jerusalem, Kilogramme, Liverpool, Madagascar, New York, Oslo, Paris, Quebec, Roma, Santiago, Tripoli, Upsala, Valencia, Washington, Xanthippe, Yokohama, Zurich
British and American armed forces had each developed their spelling alphabets before both forces adopted the ICAO alphabet during 1956. British forces adopted the RAF phonetic alphabet, which is similar to the phonetic alphabet used by the Royal Navy during World War I. At least two of the terms are sometimes still used by UK civilians to spell words over the phone, namely 'F for Freddie' and 'S for Sugar'.
The U.S. adopted the Joint Army/Navy Phonetic Alphabet during 1941 to standardize systems among all branches of its armed forces. The U.S. alphabet became known as Able Baker after the words for A and B. The United Kingdom adapted its RAF alphabet during 1943 to be almost identical to the American Joint-Army-Navy (JAN) one.
After World War II, with many aircraft and ground personnel from the allied armed forces, "Able Baker" continued to be used for civil aviation. But many sounds were unique to English, so an alternative "Ana Brazil" alphabet was used in Latin America. But the International Air Transport Association (IATA), recognizing the need for a single universal alphabet, presented a draft alphabet to the ICAO during 1947 that had sounds common to English, French, Spanish and Portuguese. After further study and modification by each approving body, the revised alphabet was implemented on 1 November 1951 for civil aviation (but it may not have been adopted by any military):[23]
Alfa, Bravo, Coca, Delta, Echo, Foxtrot, Golf, Hotel, India, Juliett, Kilo, Lima, Metro, Nectar, Oscar, Papa, Quebec, Romeo, Sierra, Tango, Union, Victor, Whisky, Extra, Yankee, Zulu
Problems were soon found with this list. Some users believed that they were so severe that they reverted to the old "Able Baker" alphabet. To identify the deficiencies of the new alphabet, testing was conducted among speakers from 31 nations, principally by the governments of the United Kingdom and the United States. Confusion among words like Delta, Nectar, Victor, and Extra, or the unintelligibility of other words during poor receiving conditions were the main problems. After much study, only the five words representing the letters C, M, N, U, and X were replaced. The ICAO sent a recording of the new Radiotelephony Spelling Alphabet to all member states in November 1955.[16][9] The final version given in the table above was implemented by the ICAO on 1 March 1956,[23] and the ITU adopted it no later than 1959 when they mandated its usage via their official publication, Radio Regulations.[24] Because the ITU governs all international radio communications, it was also adopted by all radio operators, whether military, civilian, or amateur. It was finally adopted by the IMO in 1965. During 1947 the ITU adopted the compound number words (Nadazero Unaone, etc.), later adopted by the IMO during 1965.
A spelling alphabet is used to spell parts of a message containing letters and numbers to avoid confusion, because many letters sound similar, for instance "n" and "m" or "f" and "s"; the potential for confusion increases if static or other interference is present. For instance the message "proceed to map grid DH98" could be transmitted as "proceed to map grid Delta-Hotel-Niner-Ait". Using "Delta" instead of "D" avoids confusion between "DH98" and "BH98" or "TH98". The unusual pronunciation of certain numbers was designed to reduce confusion.
In addition to the traditional military usage, civilian industry uses the alphabet to avoid similar problems in the transmission of messages by telephone systems. For example, it is often used in the retail industry where customer or site details are spoken by telephone (to authorize a credit agreement or confirm stock codes), although ad hoc coding is often used in that instance. It has been used often by information technology workers to communicate serial/reference codes (which are often very long) or other specialised information by voice. Most major airlines use the alphabet to communicate Passenger Name Records (PNRs) internally, and in some cases, with customers. It is often used in a medical context as well, to avoid confusion when transmitting information.
Several letter codes and abbreviations using the spelling alphabet have become well-known, such as Bravo Zulu (letter code BZ) for "well done",[25]Checkpoint Charlie (Checkpoint C) in Berlin, and Zulu Time for Greenwich Mean Time or Coordinated Universal Time. During the Vietnam War, the The U.S. government referred to the Viet Cong guerrillas and the group itself as VC, or Victor Charlie; the name "Charlie" became synonymous with this force.
Adam, Boston, Chicago, Denver, Edward, Frank, George, Henry, Ida, John, King, Lincoln, Mary, New York, Ocean, Peter, Queen, Roger, Sugar, Thomas, Union, [Victor?], William, X-Ray, Young, Zero
Many unofficial spelling alphabets are in use that are not based on a standard, but are based on words the transmitter can remember easily, including first names, states, or cities. The LAPD phonetic alphabet has many first names. The German spelling alphabet ("Deutsches Funkalphabet" (literally "German Radio Alphabet")) also uses first names. Also, during the Vietnam war, soldiers used 'Cain' instead of 'Charlie' because 'Charlie' meant Viet Cong (Charlie being short for Victor Charlie, the NATO alphabet spelling of the initials VC).
Certain languages' standard alphabets have letters, or letters with diacritics (e.g., umlauts), that do not exist in the English alphabet. If these letters have two-letter ASCII substitutes, the ICAO/NATO code words for the two letters are used.
In Spanish the word "oo" is used for .
In German and Swedish, Alfa-Alfa (aa) is used for "", Alfa-Echo (ae) for "", Oscar-Echo (oe) for "", Sierra-Sierra (ss) for "", and Uniform-Echo (ue) for "".[28] Alternatively, Swedish may use ke, rlig and sten for the accented letters.
In Danish and Norwegian the letters "", "" and "" have their own code words. In Danish gir, dis and se represent the three letters,[29] while in Norwegian the three code words are gir, rnulf and got for civilians and rlig, sten and se for military personnel.[30]
Czech "", historically uo, is Uniform-Oscar (uo).
In Finnish there are special code words for the letters , and . ke is used to represent , iti is used for and ljy for . These code words are used only in national operations, the last remnants of the Finnish radio alphabet.[31]
Estonian has 4 special letters, , , and . nne represents , rni for , bik for and lle for .
Malay replaces letter L with London", since the word Lima in Malay means number 5 (five).
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Genetic Engineering | MSPCA-Angell
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The MSPCAbelieves scientists ability to clone animals, to alter the genetic makeup of an animal, and to transfer pieces of genetic material from one species to another raises serious concerns for animals and humans alike.
This pagewill explore issues related to genetic engineering, transgenic animals, and cloned animals. It will examine the implications of genetic engineering on human and animal welfare and will touch on some related moral and ethical concerns that our society has so far failed to completely address.
Definitions
Problems related to the physical and psychological well-being of cloned and transgenic animals, significant ethical concerns about the direct manipulation of genetic material, and questions about the value of life itself must all be carefully weighed against the potential benefits of genetic engineering for disease research, agricultural purposes, vaccine development, pharmaceutical products, and organ transplants.
Genetic engineering is, as yet, an imperfect science that yields imperfect results.
Changes in animal growth and development brought about by genetic engineering and cloning are less predictable, more rapid, and often more debilitating than changes brought about through the traditional process of selective breeding.
This is especially apparent with cloning. Success rates are incredibly low; on average, less than 5% of cloned embryos are born and survive.
Clones are created at a great cost to animals. The clones that are successful, as well as those that do not survive and the surrogates who carry them, suffer greatly.Many of the cloned animals that do survive are plagued by severe health problems.
Offspring suffer from severe birth defects such as Large Offspring Syndrome (LOS), in which the cloned offspring are significantly larger than normal fetuses; hydrops, a typically fatal condition in which the mother or the fetus swells with fluid; respiratory distress; developmental problems; malformed organs; musculoskeletal deformities; or weakened immune systems, to name only a few.
Additionally, surrogates are subjected to repeated invasive procedures to harvest their eggs, implant embryos, or due to the offsprings birth defects surgical intervention to deliver their offspring. All of these problems occur at much higher rates than for offspring produced via traditional breeding methods.
Cloning increases existing animal welfare and environmental concerns related to animal agriculture.
In 1996, the birth of the ewe, Dolly, marked the first successful cloning of a mammal from adult cells. At the time of her birth, the researchers who created Dolly acknowledged the inefficiency of the new technology: it took 277 attempts to create this one sheep, and of these, only 29 early embryos developed, and an even smaller number of these developed into live fetuses. In the end, Dolly was the sole surviving clone. She was euthanized in 2003 at just 6 years of age, about half as old as sheep are expected to live, and with health problems more common in older sheep.
Since Dollys creation, the process of cloning has not demonstrated great improvement in efficiency or rates of success. A 2003 review of cloning in cattle found that less than 5% of cloned embryos transferred into surrogate cows survived; a 2016 study showedno noticeable increase in efficiency, with the success rate being about 1%.
Currently, research is focused on cloning for agricultural purposes. Used alone, or in concert with genetic engineering, the objective is to clone the best stock to reproduce whole herds or flocks with desired uniform characteristics of a specific trait, such as fast growth, leaner meat, or higher milk production. Cloning is often pursued to produce animals that grow faster so they can be slaughtered sooner and to raise more animals in a smaller space.
For example, transgenic fish are engineered to grow larger at a faster rate and cows injected with genetically engineered products to increase their productivity. Another example of this is the use of the genetically engineered drug, bovine growth hormone (BGH or BST) to increase milk production in dairy cows. This has also been associated with increased cases of udder disease, spontaneous abortion, lameness, and shortened lifespan. The use of BGH is controversial; many countries (such as Canada, Japan, Australia, and countries in the EU) do not allow it, and many consumers try to avoid it.A rise in transgenic animals used for agriculture will only exacerbate current animal welfare and environmental concerns with existing intensive farming operations.(For more information on farming and animal welfare, visit the MSPCAs Farm Animal Welfare page.)
Much remains unknown about thepotential environmental impacts of widespread cloning of animals. The creation of genetically identical animals leads to concerns about limited agricultural animal gene pools. The effects of creating uniform herds of animals and the resulting loss of biodiversity, have significant implications for the environment and for the ability of cloned herds to withstand diseases. This could make an impact on the entireagriculture industry and human food chain.
These issues became especiallyconcerning when, in 2008, the Federal Drug Administration not only approved the sale of meat from the offspring of cloned animals, but also did not require that it be labeled as such. There have been few published studies that examine the composition of milk, meat, or eggs from cloned animals or their progeny, including the safety of eating those products. The health problems associated with cloned animals, particularly those that appear healthy but have concealed illnesses or problems that appear unexpectedly later in life, could potentially pose risks to the safety of the food products derived from those animals.
Genetically Engineered Pets
Companion animals have also been cloned. The first cloned cat, CC, was created in 2001. CCs creation marked the beginning of the pet cloning industry, in which pet owners could pay to bank DNA from their companion dogs and cats to be cloned in the future. In 2005, the first cloned dog was created; later, the first commercially cloned dog followed at a cost of $50,000. Many consumers assume that cloning will produce a carbon copy of their beloved pet, but this is not the case. Even though the animals are genetically identical, they often do not resemble each other physically or behaviorally.
To date, the pet cloning industry has not been largely successful. However, efforts to make cloning a successful commercial venture are still being put forth.RBio (formerly RNL Bio), a Korean biotechnology company, planned to create a research center that would produce 1,000 cloned dogs annually by 2013. However, RBio, considered a black market cloner, failed to make any significant strides in itscloning endeavors and seems to have been replaced by other companies, such as South Korean-based Sooam Biotech, now the worlds leader in commercial pet cloning. Since 2006, Sooam has cloned over 800 dogs, in addition to other animals, such as cattle and pigs, for breed preservation and medical research.
While South Korean animal cloning expands, the interest in companion animal cloning in the United States continues to remain low. In 2009, the American company BioArts ceased its dog cloning services and ended its partnership with Sooam, stating in a press release that cloning procedures were still underdeveloped and that the cloning market itself was weak and unethical. Companion animal cloning causes concern not only because of the welfare issues inherent in the cloning process, but also because of its potential to contribute to pet overpopulation problem in the US, as millions of animals in shelters wait for homes.
Cloning and Medical Research
Cloning is also used to produce copies of transgenic animals that have been created to mimic certain human diseases. The transgenic animals are created, then cloned, producing a supply of animals for biomedical testing.
A 1980 U.S. Supreme Court decision to permit the patenting of a microorganism that could digest crude oil had a great impact on animal welfare and genetic engineering. Until that time, the U.S. Patent Office had prohibited the patenting of living organisms. However, following the Supreme Court decision, the Patent Office interpreted this ruling to extend to the patenting of all higher life forms, paving the way for a tremendous explosion of corporate investment in genetic engineering research.
In 1988, the first animal patent was issued to Harvard University for the Oncomouse, a transgenic mouse genetically modified to be more prone to develop cancers mimicking human disease. Since then, millions of transgenic mice have been produced. Transgenic rats, rabbits, monkeys, fish, chickens, pigs, sheep, goats, cows, horses, cats, dogs, and other animals have also been created.
Both expected and unexpected results occur in the process of inserting new genetic material into an egg cell. Defective offspring can suffer from chromosomal abnormalities that can cause cancer, fatal bleeding disorders, inability to reproduce, early uterine death, lack of ability to nurse, and such diseases as arthritis, diabetes, liver disease, and kidney disease.
The production of transgenic animals is of concern because genetic engineering is often used to create animals with diseases that cause intense suffering. Among the diseases that can be produced in genetically engineered research mice are diabetes, cancer, cystic fibrosis, sickle-cell anemia, Huntingtons disease, Alzheimers disease, and a rare but severe neurological condition called Lesch-Nyhansyndromethat causes the sufferer to self-mutilate. Animals carrying the genes for these diseases can suffer for long periods of time, both in the laboratory and while they are kept on the shelf by laboratory animal suppliers.
Another reason for the production of transgenic animals is pharming, in which sheep and goats are modified to produce pharmaceuticals in their milk. In 2009, the first drug produced by genetically engineered animals was approved by the FDA. The drug ATryn, used to prevent fatal blood clots in humans, is derived from goats into which a segment of human DNA has been inserted, causing them to produce an anticoagulant protein in their milk. This marks the first time a drug has been manufactured from a herd of animals created specifically to produce a pharmaceutical.
A company has also manufactured a drug produced in the milk of transgenic rabbits to treat a dangerous tissue swelling caused by a human protein deficiency. Yet another pharmaceutical manufacturer, PharmAnthene, was funded by the US Department of Defense to develop genetically engineered goats whose milk produces proteins used in a drug to treat nerve gas poisoning. The FDA also approved a drug whose primary proteins are also found in the milk of genetically engineered goats, who are kept at a farm in Framingham, Massachusetts. Additionally, a herd of cattle was recently developed that produces milk containing proteins that help to treat human emphysema. These animals are essentially used as pharmaceutical-production machines to manufacture only those substances they were genetically modified to produce; they are not used as part of the normal food supply chain for items such as meat or milk.
The transfer of animal tissues from one species to another raises potentially serious health issues for animals and humans alike.
Some animals are also genetically modified to produce tissues and organs to be used for human transplant purposes (xenotransplantation). Much effort is being focused in this area as the demand for human organs for transplantation far exceeds the supply, with pigs the current focus of this research. While efforts to date have been hampered by a pig protein that can cause organ rejection by the recipients immune system, efforts are underway to develop genetically modified swine with a human protein that would mitigate the chance of organ rejection.
Little is known about the ways in which diseases can be spread from one species to another, raising concerns for both animals and people, and calling into question the safety of using transgenic pigs to supply organs for human transplant purposes. Scientists have identified various viruses common in the heart, spleen, and kidneys of pigs that could infect human cells. In addition, new research is shedding light on particles called prions that, along with viruses and bacteria, may transmit fatal diseases between animals and from animals to humans.
Acknowledging the potential for transmission of viruses from animals to humans, the National Institutes of Health, a part of the U.S. Department of Health and Human Services,issued a moratorium in 2015 onxenotransplantation until the risks are better understood, ceasing funding until more research has been carried out. With the science of genetic engineering, the possibilities are endless, but so too are the risks and concerns.
Genetic engineering research has broad ethical and moral ramifications with few established societal guidelines.
While biotechnology has been quietly revolutionizing the science for decades, public debate in the United Statesover the moral, ethical, and physical effects of this research has been insufficient. To quote Colorado State University Philosopher Bernard Rollin, We cannot control technology if we do not understand it, and we cannot understand it without a careful discussion of the moral questions to which it gives rise.
Research into non-animal methods of achieving some of the same goals looks promising.
Researchers in the U.S. and elsewhere have found ways togenetically engineer cereal grains to produce human proteins. One example of this, developed in the early 2000s, is a strain of rice that can produce a human protein used to treat cystic fibrosis. Wheat, corn, and barley may also be able to be used in similar ways at dramatically lower financial and ethical costs than genetically engineering animals for this purpose.
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Genetic Engineering and GM Crops – Pocket K | ISAAA.org
Posted: at 5:32 pm
Over the last 50 years, the field of genetic engineering has developed rapidly due to the greater understanding of deoxyribonucleic acid (DNA) as the chemical double helix code from which genes are made. The term genetic engineering is used to describe the process by which the genetic makeup of an organism can be altered using recombinant DNA technology. This involves the use of laboratory tools to insert, alter, or cut out pieces of DNA that contain one or more genes of interest.
Developing plant varieties expressing good agronomic characteristics is the ultimate goal of plant breeders. With conventional plant breeding, however, there is little or no guarantee of obtaining any particular gene combination from the millions of crosses generated. Undesirable genes can be transferred along with desirable genes; or, while one desirable gene is gained, another is lost because the genes of both parents are mixed together and re-assorted more or less randomly in the offspring. These problems limit the improvements that plant breeders can achieve.
In contrast, genetic engineering allows the direct transfer of one or just a few genes of interest, between either closely or distantly related organisms to obtain the desired agronomic trait (Figure 1). Not all genetic engineering techniques involve inserting DNA from other organisms. Plants may also be modified by removing or switching off their own particular genes.
Source: Agricultural Biotechnology (A Lot More than Just GM Crops). http://www.isaaa.org/resources/publications/agricultural_biotechnology/download/.
Genes are molecules of DNA that code for distinct traits or characteristics. For instance, a particular gene sequence is responsible for the color of a flower or a plants ability to fight a disease or thrive in extreme environment.
The sharing of DNA among living forms is well documented as a natural phenomenon. For thousands of years, genes have moved from one organism to another. For example, Agrobacterium tumefaciens, a soil bacterium known as natures own genetic engineer, has the natural ability to genetically engineer plants. It causes crown gall disease in a wide range of broad-leaved plants, such as apple, pear, peach, cherry, almond, raspberry, and roses. The disease gains its name from the large tumor-like swellings (galls) that typically occur at the crown of the plant, just above soil level. Basically, the bacterium transfers part of its DNA to the plant, and this DNA integrates into the plants genome, causing the production of tumors and associated changes in plant metabolism.
Genetic engineering techniques are used only when all other techniques have been exhausted, i.e. when the trait to be introduced is not present in the germplasm of the crop; the trait is very difficult to improve by conventional breeding methods; and when it will take a very long time to introduce and/or improve such trait in the crop by conventional breeding methods (see Figure 2). Crops developed through genetic engineering are commonly known as transgenic crops or genetically modified (GM) crops.
Modern plant breeding is a multi-disciplinary and coordinated process where a large number of tools and elements of conventional breeding techniques, bioinformatics, molecular genetics, molecular biology, and genetic engineering are utilized and integrated.
Figure 2: Modern Plant Breeding
Source: DANIDA, 2002.
Although there are many diverse and complex techniques involved in genetic engineering, its basic principles are reasonably simple. There are five major steps in the development of a genetically engineered crop. But for every step, it is very important to know the biochemical and physiological mechanisms of action, regulation of gene expression, and safety of the gene and the gene product to be utilized. Even before a genetically engineered crop is made available for commercial use, it has to pass through rigorous safety and risk assessment procedures.
The first step is the extraction of DNA from the organism known to have the trait of interest. The second step is gene cloning, which will isolate the gene of interest from the entire extracted DNA, followed by mass-production of the cloned gene in a host cell. Once it is cloned, the gene of interest is designed and packaged so that it can be controlled and properly expressed once inside the host plant. The modified gene will then be mass-produced in a host cell in order to make thousands of copies. When the gene package is ready, it can then be introduced into the cells of the plant being modified through a process called transformation. The most common methods used to introduce the gene package into plant cells include biolistic transformation (using a gene gun) or Agrobacterium-mediated transformation. Once the inserted gene is stable, inherited, and expressed in subsequent generations, then the plant is considered a transgenic. Backcross breeding is the final step in the genetic engineering process, where the transgenic crop is crossed with a variety that possesses important agronomic traits, and selected in order to obtain high quality plants that express the inserted gene in a desired manner.
The length of time in developing transgenic plant depends upon the gene, crop species, available resources, and regulatory approval. It may take 6-15 years before a new transgenic hybrid is ready for commercial release.
Transgenic crops have been planted in different countries for twenty years, starting from 1996 to 2015. About 179.7 million hectares was planted in 2015 to transgenic crops with high market value, such as herbicide tolerant soybean, maize, cotton, and canola; insect resistant maize, cotton, potato, and rice; and virus resistant squash and papaya. With genetic engineering, more than one trait can be incorporated or stacked into a plant. Transgenic crops with combined traits are also available commercially. These include herbicide tolerant and insect resistant maize, soybean and cotton.
To date, commercial GM crops have delivered benefits in crop production, but there are also a number of products in the pipeline which will make more direct contributions to food quality, environmental benefits, pharmaceutical production, and non-food crops. Examples of these products include: rice with higher levels of iron and beta-carotene (an important micronutrient which is converted to vitamin A in the body); long life banana that ripens faster on the tree and can therefore be harvested earlier; tomatoes with high levels of flavonols, which are powerful antioxidants; arsenic-tolerant plants; edible vaccines from fruit and vegetables; and low lignin trees for paper making.
*August 2016
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