Hydrogen sulfide: the gas that fuels longevity.

J Cardiovasc Aging

Department of Internal Medicine, University of Arizona College of Medicine - Phoenix, Phoenix, AZ 85004, USA.

Published: July 2022

AI Article Synopsis

  • The study focuses on using animal models to understand the molecular factors affecting lifespan, with hopes of applying these findings to human longevity.
  • It highlights research on worms that found inhibiting protein synthesis boosts the transcription factor ATF4, which in turn enhances the production of hydrogen sulfide (HS).
  • Increased HS levels are linked to improved protein stability and cardiovascular function, suggesting that nutrient deprivation and slowed protein synthesis may contribute to longer lifespans by enhancing vital bodily functions.

Article Abstract

The molecular determinants of lifespan can be examined in animal models with the long-term objective of applying what is learned to the development of strategies to enhance longevity in humans. Here, we comment on a recent publication examining the molecular mechanisms that determine lifespan in worms, (), where it was shown that inhibiting protein synthesis increased levels of the transcription factor, ATF4. Gene expression analyses showed that ATF4 increased the expression of genes responsible for the formation of the gas, hydrogen sulfide (HS). Further examination showed that HS increased longevity in by modifying proteins in ways that stabilize their structures and enhance their functions. HS has been shown to improve cardiovascular performance in mouse models of heart disease, and clinical trials are underway to test the effects of HS on cardiovascular health in humans. These findings support the concept that nutrient deprivation, which slows protein synthesis and leads to ATF4-mediated HS production, may extend lifespan by improving the function of the cardiovascular system and other systems that influence longevity in humans.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9912355PMC
http://dx.doi.org/10.20517/jca.2022.16DOI Listing

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