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"Long
before it's in the papers"
September 21, 2011
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“Longevity gene” may be unrelated to
longevity
Sept. 21, 2011
Courtesy of the Wellcome Trust
and World
Science staff
Proteins thought to boost lifespan in several test organisms—and said to be stimulated by
certain “anti-aging” products—don’t really affect longevity, new research suggests.
That doesn’t mean lifespan cannot be extended, scientists said; it just means any techniques that have succeeded in doing so were probably not working through those proteins.
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The roundworm C.
elegans, used in some aging studies. (Image courtesy free.ed.gov)
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Previous studies had linked the natural molecules, known as sirtuins, to ageing and longevity in organisms including yeast, nematode worms and fruit flies, often used as models for the biology of human ageing. Researchers had shown that when the organisms overproduced sirtuin,
they lived longer, by as much as 50 percent in the case of nematodes.
Other research identified a link between sirtuins and dietary restriction – a sharp cutback in calories eaten, a method known to extend lifespan in many organisms, including some mammals. Research suggested that it works by activating the production of sirtuins. The studies caused much interest among scientists and others. Some dubbed the sirtuin-producing gene the “longevity gene.”
Pills and “anti-ageing” creams have also been launched containing resveratrol, a substance found in red
wine and thought to activate sirtuins.
But subsequent research has cast doubt on the claims that resveratrol activates sirtuins. A study published Sept. 21 in the journal
Nature, led by David Gems and colleagues at University College London, provides almost conclusive evidence that the effects on animal longevity seen in earlier experiments were unconnected to sirtuin, the investigators said.
“These results are very surprising. We have re-examined the key experiments linking sirtuin with longevity in animals and none seem to stand up to close scrutiny. Sirtuins, far from being a key to longevity, appear to have nothing to do with extending life,” Gems said. “But I think this is good news in a way: after all, revising old ideas can be as important as presenting new ones to assure scientific progress. This work should help to redirect scientific efforts toward those processes that really do control ageing.”
Gems and colleagues, with researchers at the University of Washington, Seattle, and Semmelweis University, Budapest, examined two strains of nematode worm, each from a different prior study. These were manipulated to have a hyperactive sirtuin gene. They did live longer than normal worms, but after precautions were taken to ensure that the only difference between the normal and test worms was higher sirtuin levels, the longevity effect was found to vanish.
Thus something else must have caused the longevity, the scientists propose. In one of the two original strains, they identified this as a mutation in a gene involved in nerve
cell development.
Working with colleagues at the University of Michigan, the U.K. researchers then examined an engineered version of the fruit fly,
Drosophila melanogaster, in which sirtuin levels were also raised. The same organism had been the subject of earlier research which seemed to show that overactivation of sirtuins increased longevity.
Gems and colleagues propose genetic factors other than sirtuins genes were the cause of the longevity. They also created a new strain of fruit fly with even higher sirtuin levels, but found that this wasn’t long-lived either.
The researchers also prepared synthetic fruitfly sirtuin and tested whether it could be activated by resveratrol, as predicted by previous claims. But neither the U.K. or U.S. laboratories, each using several techniques, could show any activation. Finally, the teams re-tested the claim that dietary restriction increases lifespan by activating sirtuins. Taking mutant fruit flies that lacked the sirtuin gene, the researchers showed that dietary restriction still increased lifespan. So dietary restriction was working independently of sirtuins, they said.
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Proteins thought to boost lifespan in several test organisms—and said to be stimulated by some “anti-aging” products—don’t really affect longevity, new research suggests.
That doesn’t mean lifespan cannot be extended, the scientists said; it just means any techniques that have succeeded in doing so were probably not working through those proteins.
Previous studies had linked the natural molecules, known as sirtuins, to ageing and longevity in organisms including yeast, nematode worms and fruit flies, often used as models for the biology of human ageing. Researchers had shown that when the organism’s genes overproduced sirtuin, it lived longer, by as much as 50% in the case of nematodes.
Other research identified a link between sirtuins and dietary restriction – a sharp cutback in calories eaten, a method known to extend lifespan in many organisms, including some mammals. Research suggested that it works by activating the production of sirtuins. The studies caused much interest among scientists and others. Some dubbed the sirtuin-producing gene the “longevity gene.”
“Anti-ageing” creams have also been launched containing resveratrol, a substance found in red and thought to activate sirtuins.
But subsequent research has cast doubt on the claims that resveratrol activates sirtuins. A study published Sept. 21 in the journal Nature, led by David Gems and colleagues at University College London, provides almost conclusive evidence that the effects on animal longevity seen in earlier experiments were unconnected to sirtuin, the investigators said.
“These results are very surprising. We have re-examined the key experiments linking sirtuin with longevity in animals and none seem to stand up to close scrutiny. Sirtuins, far from being a key to longevity, appear to have nothing to do with extending life,” Gems said. “But I think this is good news in a way: after all, revising old ideas can be as important as presenting new ones to assure scientific progress. This work should help to redirect scientific efforts toward those processes that really do control ageing.”
Gems and colleagues, with researchers at the University of Washington, Seattle, and Semmelweis University, Budapest, examined two strains of nematode worm, each from a different prior study. These were manipulated to have a hyperactive sirtuin gene. They did live longer than normal worms, but after precautions were taken to ensure that the only difference between the normal and test worms was higher sirtuin levels, the longevity effect was found to vanish.
Thus something else must have caused the longevity, the scientists propose. In one of the two original strains, they identified this as a mutation in a gene involved in the development of nerve cells.
Working with colleagues at the University of Michigan, the U.K. researchers then examined an engineered version of the fruit fly, Drosophila melanogaster, in which sirtuin levels were also raised. The same organism had been the subject of earlier research which seemed to show that overactivation of sirtuins increased longevity.
Gems and colleagues propose genetic factors other than sirtuins genes were the cause of the longevity. They also created a new strain of fruit fly with even higher sirtuin levels, but found that this wasn’t long-lived either.
The researchers also prepared synthetic fruitfly sirtuin and tested whether it could be activated by resveratrol, as predicted by previous claims. But neither the U.K. or U.S. laboratories, each using several techniques, could show any activation. Finally, the teams re-tested the claim that dietary restriction increases lifespan by activating sirtuins. Taking mutant fruit flies that lacked the sirtuin gene, the researchers showed that dietary restriction still increased lifespan. So dietary restriction was working independently of sirtuins, they said.
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