Oxidative metabolites of 5-S-cysteinyldopamine inhibit the alpha-ketoglutarate dehydrogenase complex: possible relevance to the pathogenesis of Parkinson's disease.

Abstract

A characteristic change in the substantia nigra of Parkinson's disease patients is an apparent accelerated rate of dopamine oxidation as evidenced by an increased 5-S-cysteinyldopamine (5-S-CyS-DA) to dopamine ratio. However, 5-S-CyS-DA is more easily oxidized than dopamine to give 7-(2-aminoethyl)-3,4-dihydro-5-hydroxy-2H-1,4-benzothiazine-3-carboxylic acid (DHBT-1). Previous studies have demonstrated that DHBT-1 can be accumulated by intact rat brain mitochondria and inhibits complex I but not complex II respiration. In this study, it is shown that DHBT-1 also inhibits the alpha-ketoglutarate dehydrogenase complex (alpha-KGDH) but not cytochrome c oxidase (complex IV). The inhibition of alpha-KGDH is dependent on the oxidation of DHBT-1, catalyzed by an unknown constituent of the inner mitochondrial membrane, to an electrophilic o-quinone imine that covalently modifies active site sulfhydryl residues. The latter conclusion is based on the ability of > or = equimolar glutathione to block the inhibition of alpha-KGDH by DHBT-1, without altering its rate of mitochondrial membrane-catalyzed oxidation, by scavenging the electrophilic o-quinone intermediate forming glutathionyl conjugates which have been isolated and spectroscopically characterized. Activities of mitochondrial alpha-KGDH and complex I, but not other respiratory complexes, are decreased in the parkinsonian substantia nigra. Such changes together with evidence for accelerated dopamine oxidation, increased formation of 5-S-CyS-DA and the ease of oxidation of this conjugate to DHBT-1 which inhibits alpha-KGDH and complex I, without affecting other respiratory enzyme complexes, suggests that the latter putative metabolite might be an endotoxin that contributes to the alpha-KGDH and complex I defects in Parkinson's disease.

• Authors: X M Shen, H Li, G Dryhurst
• Journal: Journal of neural transmission (Vienna, Austria : 1996) (J Neural Transm (Vienna)) Vol. 107 Issue 8-9 Pg. 959-78 ( 2000) ISSN: 0300-9564 [Print] Austria
• PMID: 11041275 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• 7-(2-aminoethyl)-3,4-dihydro-5-hydroxy-2H-1,4-benzothiazine-3-carboxylic acid
• Antioxidants
• Enzyme Inhibitors
• Thiazines
• 5-S-cysteinyldopamine
• Catalase
• Prostaglandin-Endoperoxide Synthases
• Superoxide Dismutase
• Ketoglutarate Dehydrogenase Complex
• Electron Transport Complex IV
• Dopamine

Topics

• Animals
• Antioxidants (metabolism)
• Brain (enzymology)
• Catalase (metabolism)
• Dopamine (analogs & derivatives, metabolism, pharmacology)
• Electron Transport Complex IV (metabolism)
• Enzyme Inhibitors (pharmacology)
• Intracellular Membranes (enzymology)
• Ketoglutarate Dehydrogenase Complex (antagonists & inhibitors, metabolism)
• Male
• Mitochondria (enzymology)
• Oxidation-Reduction
• Parkinson Disease (etiology, metabolism)
• Prostaglandin-Endoperoxide Synthases (metabolism)
• Rats
• Rats, Sprague-Dawley
• Superoxide Dismutase (metabolism)
• Thiazines (metabolism, pharmacology)