Author
Listed:
- Joseph A. Baur
(Harvard Medical School)
- Kevin J. Pearson
(Laboratory of Experimental Gerontology)
- Nathan L. Price
(Laboratory of Experimental Gerontology)
- Hamish A. Jamieson
(Centre for Education and Research on Ageing, and the ANZAC Research Institute University of Sydney)
- Carles Lerin
(Johns Hopkins University School of Medicine)
- Avash Kalra
(Laboratory of Experimental Gerontology)
- Vinayakumar V. Prabhu
(Gene Expression and Genomics Unit)
- Joanne S. Allard
(Laboratory of Experimental Gerontology)
- Guillermo Lopez-Lluch
(Universidad Pablo de Olavide-CSIC)
- Kaitlyn Lewis
(Laboratory of Experimental Gerontology)
- Paul J. Pistell
(Laboratory of Experimental Gerontology)
- Suresh Poosala
(Research Resources Branch)
- Kevin G. Becker
(Gene Expression and Genomics Unit)
- Olivier Boss
(Sirtris Pharmaceuticals, Inc.)
- Dana Gwinn
(The Salk Institute)
- Mingyi Wang
(Laboratory of Cardiovascular Science)
- Sharan Ramaswamy
(National Institute on Aging, National Institutes of Health)
- Kenneth W. Fishbein
(National Institute on Aging, National Institutes of Health)
- Richard G. Spencer
(National Institute on Aging, National Institutes of Health)
- Edward G. Lakatta
(Laboratory of Cardiovascular Science)
- David Le Couteur
(Centre for Education and Research on Ageing, and the ANZAC Research Institute University of Sydney)
- Reuben J. Shaw
(The Salk Institute)
- Placido Navas
(Universidad Pablo de Olavide-CSIC)
- Pere Puigserver
(Johns Hopkins University School of Medicine)
- Donald K. Ingram
(Laboratory of Experimental Gerontology
Louisiana State University System)
- Rafael de Cabo
(Laboratory of Experimental Gerontology)
- David A. Sinclair
(Harvard Medical School)
Abstract
Resveratrol (3,5,4′-trihydroxystilbene) extends the lifespan of diverse species including Saccharomyces cerevisiae, Caenorhabditis elegans and Drosophila melanogaster. In these organisms, lifespan extension is dependent on Sir2, a conserved deacetylase proposed to underlie the beneficial effects of caloric restriction. Here we show that resveratrol shifts the physiology of middle-aged mice on a high-calorie diet towards that of mice on a standard diet and significantly increases their survival. Resveratrol produces changes associated with longer lifespan, including increased insulin sensitivity, reduced insulin-like growth factor-1 (IGF-I) levels, increased AMP-activated protein kinase (AMPK) and peroxisome proliferator-activated receptor-γ coactivator 1α (PGC-1α) activity, increased mitochondrial number, and improved motor function. Parametric analysis of gene set enrichment revealed that resveratrol opposed the effects of the high-calorie diet in 144 out of 153 significantly altered pathways. These data show that improving general health in mammals using small molecules is an attainable goal, and point to new approaches for treating obesity-related disorders and diseases of ageing.
Suggested Citation
Joseph A. Baur & Kevin J. Pearson & Nathan L. Price & Hamish A. Jamieson & Carles Lerin & Avash Kalra & Vinayakumar V. Prabhu & Joanne S. Allard & Guillermo Lopez-Lluch & Kaitlyn Lewis & Paul J. Piste, 2006.
"Resveratrol improves health and survival of mice on a high-calorie diet,"
Nature, Nature, vol. 444(7117), pages 337-342, November.
Handle:
RePEc:nat:nature:v:444:y:2006:i:7117:d:10.1038_nature05354
DOI: 10.1038/nature05354
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Cited by:
- Robin Haunschild & Werner Marx, 2022.
"On Health Effects of Resveratrol in Wine,"
IJERPH, MDPI, vol. 19(5), pages 1-13, March.
- Yonghong Liu & Zhixian Wu & Jing-Ran Shan & Huaipu Yan & Er-Jun Hao & Lei Shi, 2024.
"Titanium catalyzed [2σ + 2π] cycloaddition of bicyclo[1.1.0]-butanes with 1,3-dienes for efficient synthesis of stilbene bioisosteres,"
Nature Communications, Nature, vol. 15(1), pages 1-9, December.
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