Alpha-lipoic acid supplementation protects enzymes from damage by nitrosative and oxidative stress

Biochim Biophys Acta. 2016 Jan;1860(1 Pt A):36-45. doi: 10.1016/j.bbagen.2015.09.001. Epub 2015 Sep 4.

Abstract

Background: S-nitrosylation of mitochondrial enzymes involved in energy transfer under nitrosative stress may result in ATP deficiency. We investigated whether α-lipoic acid, a powerful antioxidant, could alleviate nitrosative stress by regulating S-nitrosylation, which could result in retaining the mitochondrial enzyme activity.

Methods: In this study, we have identified the S-nitrosylated forms of subunit 1 of dihydrolipoyllysine succinyltransferase (complex III), and subunit 2 of the α-ketoglutarate dehydrogenase complex by implementing a fluorescence-based differential quantitative proteomics method.

Results: We found that the activities of these two mitochondrial enzymes were partially but reversibly inhibited by S-nitrosylation in cultured endothelial cells, and that their activities were partially restored by supplementation of α-lipoic acid. We show that protein S-nitrosylation affects the activity of mitochondrial enzymes that are central to energy supply, and that α-lipoic acid protects mitochondrial enzymes by altering S-nitrosylation levels.

Conclusions: Inhibiting protein S-nitrosylation with α-lipoic acid seems to be a protective mechanism against nitrosative stress.

General significance: Identification and characterization of these new protein targets should contribute to expanding the therapeutic power of α-lipoic acid and to a better understanding of the underlying antioxidant mechanisms.

Keywords: ATP; Antioxidant; Mitochondria; Nitric oxide (NO); Nitrosative stress (NS); Reactive oxygen species (ROS); S-nitrosylation; α-Lipoic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / biosynthesis
  • Animals
  • Cells, Cultured
  • Electron Transport Complex III / metabolism*
  • Ketoglutarate Dehydrogenase Complex / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Nitric Oxide / metabolism*
  • Oxidative Stress*
  • Thioctic Acid / pharmacology*

Substances

  • Nitric Oxide
  • Thioctic Acid
  • Adenosine Triphosphate
  • Ketoglutarate Dehydrogenase Complex
  • Electron Transport Complex III