Natural thioallyl compounds increase oxidative stress resistance and lifespan in Caenorhabditis elegans by modulating SKN-1/Nrf

Sci Rep. 2016 Feb 22:6:21611. doi: 10.1038/srep21611.

Abstract

Identification of biologically active natural compounds that promote health and longevity, and understanding how they act, will provide insights into aging and metabolism, and strategies for developing agents that prevent chronic disease. The garlic-derived thioallyl compounds S-allylcysteine (SAC) and S-allylmercaptocysteine (SAMC) have been shown to have multiple biological activities. Here we show that SAC and SAMC increase lifespan and stress resistance in Caenorhabditis elegans and reduce accumulation of reactive oxygen species (ROS). These compounds do not appear to activate DAF-16 (FOXO orthologue) or mimic dietary restriction (DR) effects, but selectively induce SKN-1 (Nrf1/2/3 orthologue) targets involved in oxidative stress defense. Interestingly, their treatments do not facilitate SKN-1 nuclear accumulation, but slightly increased intracellular SKN-1 levels. Our data also indicate that thioallyl structure and the number of sulfur atoms are important for SKN-1 target induction. Our results indicate that SAC and SAMC may serve as potential agents that slow aging.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / drug effects*
  • Aging / genetics
  • Animals
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / growth & development
  • Caenorhabditis elegans Proteins / biosynthesis*
  • Caenorhabditis elegans Proteins / genetics
  • Cysteine / administration & dosage
  • Cysteine / analogs & derivatives*
  • Cysteine / chemistry
  • DNA-Binding Proteins / biosynthesis*
  • DNA-Binding Proteins / genetics
  • Forkhead Transcription Factors / biosynthesis
  • Garlic / chemistry
  • Gene Expression Regulation / drug effects
  • Longevity / drug effects
  • Longevity / genetics*
  • Oxidative Stress / drug effects
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics

Substances

  • Caenorhabditis elegans Proteins
  • DNA-Binding Proteins
  • Forkhead Transcription Factors
  • Reactive Oxygen Species
  • S-allylmercaptocysteine
  • Transcription Factors
  • daf-16 protein, C elegans
  • skn-1 protein, C elegans
  • S-allylcysteine
  • Cysteine