Abstract
1. DL-8-Methyldihydrolipoate was shown to be a potent inhibitor of mitochondrial oxidative phosphorylation and ATP-driven energy-linked reactions. 2. ADP-stimulated respiration utilizing pyruvate + malate and succinate in both ox heart and rat liver mitochondria is inhibited; oxidative phosphorylation using pyruvate + malate, succinate and ascorbate + NNN'N'-tetramethyl-p-phenylenediamine as substrates is also inhibited; uncoupler-stimulated respiration is unaffected regardless of the substrate used. 3. Mitochondrial oligomycin-sensitive adenosine triphosphatase is inhibited in both the membrane-bound form and the purified detergent-dispersed preparation. 4. ATP-driven transhydrogenase and the ATP-driven energy-linked reduction of NAD+ by succinate in ox heart submitochondrial particles are inhibited, whereas the respiratory-chain-driven transhydrogenase is unaffected. 5. DL-8-Methyl-lipoate has no immediate effect on the above reactions, demonstrating the requirement for the reduced form for inhibition. 6. The inhibitory properties of DL-8-methyldihydrolipoate are analogous to those of oligomycin and provide further evidence of a role for lipoic acid in oxidative phosphorylation.
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Griffiths D. E., Houghton R. L. Studies on energy-linked reactions: modified mitochondrial ATPase of oligomycin-resistant mutants of Saccharomyces cerevisiae. Eur J Biochem. 1974 Jul 1;46(1):157–167. doi: 10.1111/j.1432-1033.1974.tb03608.x. [DOI] [PubMed] [Google Scholar]
- Griffiths D. E., Roberton A. M. Energy-linked reactions in mitochondria. Studies on the reduction of NAD+ by succinate. Biochim Biophys Acta. 1966 Jan 11;113(1):13–26. doi: 10.1016/s0926-6593(66)80116-9. [DOI] [PubMed] [Google Scholar]
- Griffiths D. E., Roberton A. M. Energy-linked reactions in mitochondria: studies on the mechanism of the energy-linked transhydrogenase reaction. Biochim Biophys Acta. 1966 Jun 15;118(3):453–464. doi: 10.1016/s0926-6593(66)80089-9. [DOI] [PubMed] [Google Scholar]
- Griffiths D. E. Studies of energy-linked reactions. Net synthesis of adenosine triphosphate by isolated adenosine triphosphate synthase preparations: a role for lipoic acid and unsaturated fatty acids. Biochem J. 1976 Dec 15;160(3):809–812. doi: 10.1042/bj1600809. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hatefi Y., Stiggall D. L., Galante Y., Hanstein W. G. Mitochondrial ATP-Pi exchange complex. Biochem Biophys Res Commun. 1974 Nov 6;61(1):313–321. doi: 10.1016/0006-291x(74)90568-3. [DOI] [PubMed] [Google Scholar]
- REED L. J. The chemistry and function of lipoic acid. Adv Enzymol Relat Subj Biochem. 1957;18:319–347. doi: 10.1002/9780470122631.ch8. [DOI] [PubMed] [Google Scholar]
- STOKSTAD E. L. Discussion: biological activities of analogues and derivatives of thioctic acid. Fed Proc. 1954 Sep;13(3):712–714. [PubMed] [Google Scholar]
- Schmidt U., Grafen P., Altland K., Goedde H. W. Biochemistry and chemistry of lipoic acids. Adv Enzymol Relat Areas Mol Biol. 1969;32:423–469. doi: 10.1002/9780470122778.ch10. [DOI] [PubMed] [Google Scholar]
- Serrano R., Kanner B. I., Racker E. Purification and properties of the proton-translocating adenosine triphosphatase complex of bovine heart mitochondria. J Biol Chem. 1976 Apr 25;251(8):2453–2461. [PubMed] [Google Scholar]
