Mitochondrial Stress as a Central Player in the Pathogenesis of Hypoxia-Related Myocardial Dysfunction: New Insights

Int J Med Sci. 2024 Sep 23;21(13):2502-2509. doi: 10.7150/ijms.99359. eCollection 2024.

Abstract

Hypoxic injury is a critical pathological factor in the development of various cardiovascular diseases, such as congenital heart disease, myocardial infarction, and heart failure. Mitochondrial quality control is essential for protecting cardiomyocytes from hypoxic damage. Under hypoxic conditions, disruptions in mitochondrial homeostasis result in excessive reactive oxygen species (ROS) production, imbalances in mitochondrial dynamics, and initiate pathological processes including oxidative stress, inflammatory responses, and apoptosis. Targeted interventions to enhance mitochondrial quality control, such as coenzyme Q10 and statins, have shown promise in mitigating hypoxia-induced mitochondrial dysfunction. These treatments offer potential therapeutic strategies for hypoxia-related cardiovascular diseases by regulating mitochondrial fission and fusion, restoring mitochondrial biogenesis, reducing ROS production, and promoting mitophagy.

Keywords: Hypoxia; Mitochondrial Homeostasis; Myocardial Injury.

Publication types

  • Review

MeSH terms

  • Animals
  • Apoptosis
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use
  • Hypoxia* / complications
  • Hypoxia* / metabolism
  • Hypoxia* / physiopathology
  • Mitochondria / metabolism
  • Mitochondria, Heart / metabolism
  • Mitochondria, Heart / pathology
  • Mitochondrial Dynamics
  • Mitophagy*
  • Myocytes, Cardiac / metabolism
  • Oxidative Stress*
  • Reactive Oxygen Species* / metabolism
  • Ubiquinone / analogs & derivatives
  • Ubiquinone / therapeutic use

Substances

  • Reactive Oxygen Species
  • Ubiquinone
  • coenzyme Q10
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors