Oxidative stress in vascular senescence: lessons from successfully aging species
Zoltan Ungvari1, Rochelle Buffenstein, Steven N Austad
1Department of Physiology, New York Medical College, Valhalla, New York 10595, USA. zoltan_ungvari@nymc.edu
Insights
Cardiovascular aging involves oxidative stress and inflammation. Studying long-lived species like naked mole-rats may reveal secrets to delaying heart disease and stroke in humans.
Area of Science:
- Gerontology
- Cardiovascular Science
- Comparative Biology
Background:
- Cardiovascular disease is a primary cause of death in the elderly.
- Oxidative stress and inflammation are key factors in cardiovascular aging.
- Understanding these mechanisms can lead to interventions for age-related heart conditions.
Purpose of the Study:
- To review evidence on oxidative stress and inflammation in cardiovascular aging.
- To explore the potential of long-lived species as models for healthy cardiovascular aging.
- To identify mechanisms for delaying cardiovascular aging.
Main Methods:
- Review of existing literature on cardiovascular aging, oxidative stress, and inflammation.
- Comparative analysis of aging patterns and oxidative stress resistance in mammals with varying lifespans.
- Discussion of specific long-lived, mouse-sized species as potential research models.
Main Results:
- Evidence strongly supports the roles of oxidative stress and inflammation in cardiovascular aging.
- Significant variation exists in mammalian lifespan and cardiovascular aging.
- Long-lived species offer unique insights into successful cardiovascular aging.
Conclusions:
- Comparative studies of oxidative stress and redox signaling in long-lived species can elucidate mechanisms for delaying cardiovascular aging.
- Species like the naked mole-rat, white-footed mouse, and little brown bat are promising models.
- These models can help test the oxidative stress theory of aging and identify strategies to promote cardiovascular health in the elderly.
Abstract:
Cardiovascular disease is a main cause of morbidity and a leading cause of death of elderly Americans. Studies identifying the pathophysiological mechanisms underlying cardiovascular aging hold promise to develop treatments to delay/prevent coronary artery disease and stroke in the elderly. Evidence supporting the roles of oxidative stress and inflammation in the cardiovascular aging process is presented in detail in this review. Mammalian lifespan ranges hundred-fold and we propose that long-living species may be useful models for successful cardiovascular aging in humans. Comparative studies exploiting the large differences in maximum lifespan potential and cardiovascular aging patterns may be particularly relevant. Comparisons of mechanisms related to oxidative stress, oxidative stress resistance and redox signaling between long-living species and shorter-living ones may elucidate key mechanisms for delaying cardiovascular aging. We discuss the potential use of three long-lived but mouse-sized mammalian species, the naked mole-rat (Heterocephalus glaber), the white-footed mouse (Peromyscus leucopus) and the little brown bat (Myotis lucifugus) to test predictions of the oxidative stress theory of aging and elucidate mechanisms by which cardiovascular aging can be delayed.
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