Epicatechin modulates stress-resistance in C. elegans via insulin/IGF-1 signaling pathway

PLoS One. 2019 Jan 28;14(1):e0199483. doi: 10.1371/journal.pone.0199483. eCollection 2019.

Abstract

The nematode Caenorhabditis elegans has been used to examine the influence of epicatechin (EC), an abundant flavonoid in the human diet, in some stress biomarkers (ROS production, lipid peroxidation and protein carbonylation). Furthermore, the ability of EC to modulate the expression of some key genes in the insulin/IGF-1 signaling pathway (IIS), involved in longevity and oxidative or heat shock stress response, has also been explored. The final aim was to contribute to the elucidation of the mechanisms involved in the biological effects of flavonoids. The results showed that EC-treated wild-type C. elegans exhibited increased survival and reduced oxidative damage of biomolecules when submitted to thermal stress. EC treatment led to a moderate elevation in ROS levels, which might activate endogenous mechanisms of defense protecting against oxidative insult. The enhanced stress resistance induced by EC was found to be mediated through the IIS pathway, since assays in daf-2, age-1, akt-1, akt-2, sgk-1, daf-16, skn-1 and hsf-1 loss of function mutant strains failed to show any heat-resistant phenotype against thermal stress when treated with EC. Consistently, EC treatment upregulated the expression of some stress resistance associated genes, such as gst-4, hsp-16.2 and hsp-70, which are downstream regulated by the IIS pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Catechin / pharmacology*
  • Insulin / genetics
  • Insulin / metabolism*
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism*
  • Lipid Peroxidation / drug effects
  • Oxidative Stress / drug effects*
  • Oxidative Stress / genetics
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects*
  • Signal Transduction / genetics

Substances

  • Caenorhabditis elegans Proteins
  • Insulin
  • Reactive Oxygen Species
  • Insulin-Like Growth Factor I
  • Catechin

Grants and funding

This work was funded by MINECO (Spanish National Projects AGL2015-64522-C2 to CS-B and BFU2015-64408-P to AM-V) and FEDER-Interreg España-Portugal Programme (Ref. 0377_IBERPHENOL_6_E). Author BA-D is recipient of a PhD fellowship from the Junta de Castilla y Leon (Orden EDU/310/2015). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.