PICOT alleviates myocardial ischemia-reperfusion injury by reducing intracellular levels of reactive oxygen species

Biochem Biophys Res Commun. 2017 Apr 15;485(4):807-813. doi: 10.1016/j.bbrc.2017.02.136. Epub 2017 Feb 28.

Abstract

Excessive generation of reactive oxygen species (ROS) is one of the main causes of myocardial ischemia-reperfusion (I/R) injury. In this study, we investigated the role of protein kinase C-interacting cousin of thioredoxin (PICOT; Grx3) during myocardial I/R using PICOT transgenic (TG) and knockdown (KD) mice. Infarction and apoptosis were attenuated in PICOT TG mice but exacerbated in PICOT KD mice upon I/R. In parallel, I/R-induced generation of ROS was attenuated in PICOT TG mice but exacerbated in PICOT KD mice. Angiotensin II (AngII)-mediated increases in ROS and free iron levels were also attenuated in cardiomyocytes isolated from PICOT TG mice but exacerbated in cardiomyocytes from PICOT KD mice. Accordingly, H2O2-mediated cell death was attenuated in cardiomyocytes isolated from PICOT TG mice but exacerbated in cardiomyocytes from PICOT KD mice. Taken together, these data show that PICOT alleviates myocardial I/R injury by regulating intracellular ROS and free iron levels. We suggest that PICOT presents a novel therapeutic strategy for myocardial I/R injury.

Keywords: Free iron; Glutaredoxin 3; Heart; Ischemia-reperfusion injury; PICOT; ROS.

MeSH terms

  • Angiotensin II / pharmacology
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Hydrogen Peroxide / pharmacology
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism*
  • Iron / metabolism
  • Male
  • Mice, Knockout
  • Mice, Transgenic
  • Microscopy, Fluorescence
  • Myocardial Reperfusion Injury / genetics
  • Myocardial Reperfusion Injury / metabolism*
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism*
  • Oxidants / pharmacology
  • Protein Disulfide Reductase (Glutathione)
  • Reactive Oxygen Species / metabolism*

Substances

  • Carrier Proteins
  • Oxidants
  • Reactive Oxygen Species
  • Angiotensin II
  • Hydrogen Peroxide
  • Iron
  • Protein Disulfide Reductase (Glutathione)
  • Txnl2 protein, mouse