Lipidomic Alterations and PPAR α Activation Induced by Resveratrol Lead to Reduction in Lesion Size in Endometriosis Models

Oxid Med Cell Longev. 2021 Sep 11:2021:9979953. doi: 10.1155/2021/9979953. eCollection 2021.

Abstract

Endometriosis is an estrogen-dependent chronic inflammatory disease that affects approximately 10% of women of reproductive age and up to 50% of women with infertility. The heterogeneity of the disease makes accurate diagnosis and treatment a clinical challenge. In this study, we generated two models of endometriosis: the first in rats and the second using human ectopic endometrial stromal cells (HEcESCs) derived from the lesion tissues of endometriosis patients. We then applied resveratrol to assess its therapeutic potential. Resveratrol intervention had significant efficacy to attenuate lesion size and to rectify aberrant lipid profiles of model rats. Lipidomic analysis revealed significant lipidomic alterations, including notable increases of sphingolipids and decreases of both glycerolipids and most phospholipids. Upon resveratrol application, both proliferation capacity and invasiveness parameters decreased, and the early apoptosis proportion increased for HEcESCs. The activation of PPARα was also noted as a factor potentially contributing to recovery from endometriosis in both models. Our study provides valuable insight into the mechanisms of resveratrol in endometriosis and therefore strengthens the potential for optimizing resveratrol treatment for this disease.

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Apoptosis
  • Disease Models, Animal
  • Endometriosis / drug therapy*
  • Endometriosis / metabolism
  • Endometriosis / pathology
  • Endometrium / drug effects*
  • Endometrium / metabolism
  • Female
  • Gene Expression Profiling
  • Humans
  • Lipid Metabolism / drug effects*
  • Lipidomics
  • PPAR alpha / genetics
  • PPAR alpha / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Resveratrol / pharmacology*
  • Stromal Cells / drug effects
  • Stromal Cells / metabolism

Substances

  • Antioxidants
  • PPAR alpha
  • Resveratrol