The role of NADPH oxidases in diabetic cardiomyopathy

Biochim Biophys Acta Mol Basis Dis. 2018 May;1864(5 Pt B):1908-1913. doi: 10.1016/j.bbadis.2017.07.025. Epub 2017 Jul 25.

Abstract

Systemic changes during diabetes such as high glucose, dyslipidemia, hormonal changes and low grade inflammation, are believed to induce structural and functional changes in the cardiomyocyte associated with the development of diabetic cardiomyopathy. One of the hallmarks of the diabetic heart is increased oxidative stress. NADPH-oxidases (NOXs) are important ROS-producing enzymes in the cardiomyocyte mediating both adaptive and maladaptive changes in the heart. NOXs have been suggested as a therapeutic target for several diabetic complications, but their role in diabetic cardiomyopathy is far from elucidated. In this review we aim to provide an overview of the current knowledge regarding the understanding of how NOXs influences cardiac adaptive and maladaptive processes in a "diabetic milieu". This article is part of a Special issue entitled Cardiac adaptations to obesity, diabetes and insulin resistance, edited by Professors Jan F.C. Glatz, Jason R.B. Dyck and Christine Des Rosiers.

Keywords: Diabetic cardiomyopathy; Metabolism; NADPH oxidases; Obesity and insulin resistance; Oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptation, Physiological
  • Animals
  • Blood Glucose / metabolism
  • Calcium / metabolism
  • Calcium Signaling
  • Diabetes Mellitus / enzymology*
  • Diabetes Mellitus / pathology
  • Diabetes Mellitus / physiopathology
  • Diabetic Cardiomyopathies / enzymology*
  • Diabetic Cardiomyopathies / pathology
  • Diabetic Cardiomyopathies / physiopathology
  • Energy Metabolism
  • Heart / physiopathology
  • Humans
  • Insulin Resistance
  • Lipids / blood
  • Myocytes, Cardiac / enzymology*
  • Myocytes, Cardiac / pathology
  • NADPH Oxidases / metabolism*
  • Oxidative Stress
  • Reactive Oxygen Species / metabolism

Substances

  • Blood Glucose
  • Lipids
  • Reactive Oxygen Species
  • NADPH Oxidases
  • Calcium