Inhibition of the alpha-ketoglutarate dehydrogenase-mediated reactive oxygen species generation by lipoic acid

J Neurochem. 2009 May:109 Suppl 1:222-9. doi: 10.1111/j.1471-4159.2009.05942.x.

Abstract

Dihydrolipoamide dehydrogenase (LADH) is a flavo-enzyme that serves as a subunit of alpha-ketoglutarate dehydrogenase complex (alpha-KGDHC). Reactive oxygen species (ROS) generation by alpha-KGDHC has been assigned to LADH (E3 subunit) and explained by the diaphorase activity of E3. Dysfunctions of alpha-KGDHC and concurrent ROS production have been implicated in neurodegeneration, ischemia-reperfusion, and other pathological conditions. In this work we investigated the in-depth details of ROS generation by isolated LADH and alpha-KGDHC. We found a parallel generation of superoxide and hydrogen peroxide by the E3 subunit of alpha-KGDHC which could be blocked by lipoic acid (LA) acting on a site upstream of the E3 subunit. The pathologically relevant ROS generation (at high NADH/NAD+ ratio and low pH) in the reverse mode of alpha-KGDHC could also be inhibited by LA. Our results contradict the previously proposed mechanism for pH-dependent ROS generation by LADH, showing no disassembling of the E3 functional homodimer at acidic pH using a physiologically relevant method for the examination. It is also suggested that LA could be beneficial in reducing the cell damage related to excessive ROS generation under pathological conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology*
  • Dihydrolipoamide Dehydrogenase / metabolism
  • Hydrogen Peroxide / metabolism
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Ketoglutarate Dehydrogenase Complex / antagonists & inhibitors*
  • Ketoglutarate Dehydrogenase Complex / metabolism*
  • Male
  • Membrane Potentials / drug effects
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / enzymology
  • Mitochondria / metabolism
  • Mitochondrial Membranes / drug effects
  • Oxygen Consumption / drug effects
  • Photometry
  • Reactive Oxygen Species / metabolism*
  • Spectrophotometry, Ultraviolet
  • Superoxides / metabolism
  • Thioctic Acid / pharmacology*

Substances

  • Antioxidants
  • Reactive Oxygen Species
  • Superoxides
  • Thioctic Acid
  • Hydrogen Peroxide
  • Ketoglutarate Dehydrogenase Complex
  • Dihydrolipoamide Dehydrogenase