Gastrodin pretreatment alleviates myocardial ischemia/reperfusion injury through promoting autophagic flux

Biochem Biophys Res Commun. 2018 Sep 18;503(4):2421-2428. doi: 10.1016/j.bbrc.2018.06.171. Epub 2018 Jul 3.

Abstract

Gastrodin (GAS), a monomeric component exacted from the herb Gastrodia elata Bl, may have cardioprotective effects during injury caused by myocardial ischemia/reperfusion (I/R). For the significant role of autophagy in I/R process, we targeted to explore whether autophagy was contributing to the GAS-induced protective effects during I/R procedure. Male C57BL/6 mice were subjected to reversible left coronary artery ligation and cultured neonatal rat cardiomyocytes (NRCs) exposed to hypoxia were preconditioned with GAS prior to ischemia or hypoxia, following reperfusion for 2 h or re-oxygennation for 3 h respectively. Our results demonstrated that GAS pretreatment increased autophagy and reduced apoptosis during I/R, this effect was weakened by co-treatment with the autophagic flux inhibitor chloroquine (Cq). Compared to mice subjected solely to I/R, GAS-pretreated mice had a notably smaller heart infarct size and an elevation in cardiac function. In GAS-pretreated NRCs, WB data showed that autophagy was promoted (expression of p62 was inhibited and LC3II was increased). In addition, tandem fluorescent mRFP-GFP-LC3 assays illustrated that autophagosomes were degraded duo to an increase in autophagic flux. Co-administration of Cq blocked the autophagic flux. Furthermore, GAS pretreatment increased the mitochondrial membrane potential of NRCs with subjected to H/R and increased the cardiomyocyte survival rate. These protective effects were reversed with Cq. Besides, GAS-induced the enhaucement of autophagy may correlated with activating AMP-activated protein kinase (AMPK) phosphorylation and reduced Mammalian target of rapamycin (mTOR) phosphorylation, which was abrogated by Compound C (Com C, AMPK-specific inhibitor). Our results establish that GAS pretreatment attenuates myocardial I/R injury by increasing autophagic flux aimed at eliminating dysfunctional mitochondria, therefore protecting neighbouring mitochondria and cardiomyocytes.

Keywords: Apoptosis; Autophagy; Gastrodin; Ischemia/reperfusion; Mitochondrial function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • Animals
  • Apoptosis / drug effects
  • Autophagy / drug effects*
  • Benzyl Alcohols / chemistry
  • Benzyl Alcohols / therapeutic use*
  • Cardiotonic Agents / chemistry
  • Cardiotonic Agents / therapeutic use*
  • Cells, Cultured
  • Gastrodia / chemistry
  • Glucosides / chemistry
  • Glucosides / therapeutic use*
  • Male
  • Membrane Potential, Mitochondrial / drug effects
  • Mice, Inbred C57BL
  • Myocardial Reperfusion Injury / drug therapy*
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / pathology
  • Myocytes, Cardiac / drug effects*
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / pathology
  • Phosphorylation / drug effects
  • Protein Kinases / metabolism
  • Rats
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Benzyl Alcohols
  • Cardiotonic Agents
  • Glucosides
  • gastrodin
  • Protein Kinases
  • TOR Serine-Threonine Kinases
  • AMP-Activated Protein Kinase Kinases