The interaction of Q analogs, particularly hydroxydecyl benzoquinone (idebenone), with the respiratory complexes of heart mitochondria.

Abstract:

:We have studied the interaction of idebenone (2,3-dimethoxy-5-methy-6-(10-hydroxy)decyl-1,4-benzoquinone) with the energy-conserving complexes of the respiratory chain in beef heart mitochondria and compared its energetic efficiency with that of other analogs of coenzyme Q. Idebenone is a very effective substrate for succinate:Q reductase and ubiquinol:cytochrome c reductase, but it is clearly a poor substrate for NADH:Q reductase (complex I). Indeed, idebenone is a strong inhibitor of both the redox and proton pumping activity of complex I, showing effects in part similar to those of coenzyme Q-2. However, the mechanism of idebenone interaction with complex I may be different from that of Q-2 because of its different sensitivity to inhibitors. The possible relevance of the present findings to the therapeutic use of idebenone is discussed.

journal_name

Arch Biochem Biophys

authors

Esposti MD,Ngo A,Ghelli A,Benelli B,Carelli V,McLennan H,Linnane AW

doi

10.1006/abbi.1996.0267

subject

Has Abstract

pub_date

1996-06-15 00:00:00

pages

395-400

issue

2

eissn

0003-9861

issn

1096-0384

pii

S0003-9861(96)90267-2

journal_volume

330

pub_type

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