Compound SRT1720 Improves Health, Increases Lifespan of Obese Mice
Mice given the highest doses saw mean lifespan increase by 44 percent; improved heart, pancreas, liver function
Aug. 19, 2011 - Obese male mice were given a synthetic compound called SRT1720 and their lives become healthier and, more importantly,
they lived longer than obese mice that did not get the magical compound. Researchers say the treated mice experienced improvements in the
function of the liver, pancreas and heart.
“This study has interesting implications for research on the biology of aging. It demonstrates that years of healthy
life can be extended in an animal model of diet-induced obesity by a synthetic compound that modulates a gene pathway associated with aging,”
said Richard J. Hodes, M.D. and Director of the National Institute on Aging (NIA), which supported the study
More research is needed to assess the relevance of these findings in people, Hodes and the researchers noted.
SRT1720, a patented molecule, has been shown to activate the SIRT1enzyme, part of a class of enzymes called sirtuins.
Sirtuins have been previously implicated in aging processes and are thought to contribute to the positive effects of dietary restriction (also
known as calorie restriction) in higher organisms, including nonhuman primates.
In this study, scientists compared the health of 1-year-old, or middle-aged, male mice fed a high-fat diet with a high
dose of SRT1720, a low dose of SRT1720 or no SRT1720. Additionally, these mice were compared to a control group of 1-year-old male mice fed a
“As we hypothesized, SRT1720 mimics dietary restriction, moderating many of the harmful effects of the high-fat diet and
obesity. Furthermore, we found that the higher dose of the compound had a stronger effect and there were no signs of toxicity from SRT1720
even after 80 weeks of treatment,” said study leader and senior author Rafael de Cabo, Ph.D., of the Laboratory of Experimental Gerontology at
Scientists reported changes caused by SRT1720 in following areas:
● Lifespan. While all mice on the high-fat diet gained weight, mice treated with SRT1720 had an increased average and
maximum lifespan compared to mice on the high-fat diet without SRT1720. From birth, the mice on the higher dose lived an average of 18 percent
longer, and the mice on the lower dose lived an average of 4 percent longer than the mice on the high-fat diet without SRT1720. From 56 weeks
of age, mean lifespan in low-dose mice increased by 11 percent and in high-dose mice by 44 percent.
● Liver. Mice treated with SRT1720 had less fat accumulation on their livers compared to non-treated, high-fat-diet
mice. Scientists also tested liver function using two measurements. In both tests, mice treated with SRT1720 demonstrated better liver
function than non-treated mice on a high-fat diet, but only one test showed the liver of treated mice to have equal function as mice on
standard diet. Livers of treated mice were smaller than those from untreated mice on a high-fat diet, although they were still larger than
livers of mice on a standard diet. In addition, SRT1720 suppressed liver inflammation and protected mice against cell death in the liver.
● Pancreas. SRT1720 protected high-fat-diet mice from resistance to insulin, which is often associated with obesity
and can precede diabetes. Glucose (blood sugar) measurements were approximately equal for all groups of mice, including mice on a standard
diet. Insulin levels were approximately double in mice on the high-fat diet without SRT1720 compared to mice on the standard diet and on a
high-fat diet with SRT1720.
● Heart. High-density lipoprotein (HDL), associated with good cardiovascular health, was highest in mice on a high-fat
diet with a high dose of SRT1720, even compared to mice on a standard diet. SRT1720 protected mice against cell death in the heart and
suppressed inflammation. All groups of mice on a high-fat diet experienced the same increase in cholesterol, compared to mice on a standard
● Exercise and oxygen metabolism. Mice on a high-fat diet had higher levels of oxygen consumption during periods
typically characterized by less activity. SRT1720 reversed this trend; treated mice had lower resting levels of oxygen. High-fat-diet mice
with no or a low dose of SRT1720 were less active than mice on a high dose of SRT1720 or on a standard diet.
● Genes. SRT1720 suppresses genes typically expressed in mice on a high-fat diet. For example, SRT1720 suppressed
genes that are associated with aging in the liver and previously identified as associated with aging in the kidney and brain.
To verify that the positive health effects caused by SRT1720 were, at least in part, dependent on the Sirt1 pathway,
scientists conducted a series of experiments using cell cultures. The researchers also assessed changes to mitochondrial respiration in adult
Sirt1-specific knockout mice. The tests showed that SRT1720 did not have an effect in mice or cultures lacking the Sirt1 gene although it did
have an effect in mice and cultures with Sirt1.
While the findings are promising, scientists emphasize the limitations of their research.
“In mice, SRT1720 reversed many of the health problems associated with a high-fat diet and did not have toxic side
effects, but it is too early to know whether these findings could be replicated in other animal models, much less humans,” said de Cabo. “The
bottom line is that we need much more research before considering SRT1720 or related compounds as a possible treatment for diseases of aging.”
The study is a collaborative effort between the laboratories of de Cabo; James L. Ellis of Sirtris, and David A.
Sinclair, Ph.D., co-director of the Glenn Laboratories for Molecular Biology of Aging at Harvard Medical School, Boston and consultant to
Sirtris. Researchers from the following institutions also collaborated in the study: University of Pennsylvania School of Medicine,
Philadelphia; University of Oklahoma Health Sciences Center, Oklahoma City; École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland;
University of Michigan, Ann Arbor; and University of Kentucky, Lexington.
This research was performed under a Cooperative Research and Development Agreement between the NIA and Sirtris, a
GlaxoSmithKline company. The study was primarily conducted by the NIA, part of the National Institutes of Health, and wass published online in
the Thursday, August 18, issue of Scientific Reports.
The NIA leads the federal effort supporting and conducting research on aging and the medical, social and behavioral
issues of older people. For more information on research and aging, go to
About the National Institutes of Health (NIH): NIH, the nation's medical research agency, includes 27 Institutes and
Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting
basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases.
For more information about NIH and its programs, visit
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