Interplay between NADH oxidation by complex I, glutathione redox state and sirtuin-3, and its role in the development of insulin resistance

Biochim Biophys Acta Mol Basis Dis. 2020 Aug 1;1866(8):165801. doi: 10.1016/j.bbadis.2020.165801. Epub 2020 Apr 16.

Abstract

Metabolic diseases are characterized by high NADH/NAD+ ratios due to excessive electron supply, causing defective mitochondrial function and impaired sirtuin-3 (SIRT-3) activity, the latter driving to oxidative stress and altered fatty acid β-oxidation. NADH is oxidized by the complex I in the electron transport chain, thereby factors inhibiting complex I like acetylation, cardiolipin peroxidation, and glutathionylation by low GSH/GSSG ratios affects SIRT3 function by increasing the NADH/NAD+ ratio. In this review, we summarized the evidence supporting a role of the above events in the development of insulin resistance, which is relevant in the pathogenesis of obesity and diabetes. We propose that maintenance of proper NADH/NAD+ and GSH/GSSG ratios are central to ameliorate insulin resistance, as alterations in these redox couples lead to complex I dysfunction, disruption of SIRT-3 activity, ROS production and impaired β-oxidation, the latter two being key effectors of insulin resistance.

Keywords: Diabetes; Lipid peroxidation; Liver; Mitochondria; Obesity; Skeletal muscle.

Publication types

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

MeSH terms

  • Animals
  • Cardiolipins / metabolism
  • Diabetes Mellitus / genetics
  • Diabetes Mellitus / metabolism*
  • Diabetes Mellitus / pathology
  • Electron Transport Complex I / genetics
  • Electron Transport Complex I / metabolism*
  • Glutathione / metabolism
  • Humans
  • Insulin Resistance / genetics*
  • Liver / metabolism
  • Liver / pathology
  • Mice
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • NAD / metabolism
  • Obesity / genetics
  • Obesity / metabolism*
  • Obesity / pathology
  • Oxidation-Reduction
  • Oxidative Stress
  • Reactive Oxygen Species / metabolism
  • Sirtuin 3 / genetics
  • Sirtuin 3 / metabolism*

Substances

  • Cardiolipins
  • Reactive Oxygen Species
  • NAD
  • SIRT3 protein, human
  • Sirtuin 3
  • Electron Transport Complex I
  • Glutathione