Literature DB >> 7575440

Major changes in complex I activity in mitochondria from aged rats may not be detected by direct assay of NADH:coenzyme Q reductase.

M L Genova1, C Castelluccio, R Fato, G Parenti Castelli, M Merlo Pich, G Formiggini, C Bovina, M Marchetti, G Lenaz.   

Abstract

We have investigated the respiratory activities and the concentrations of respiratory chain components of mitochondria isolated from the livers and hearts of two groups of rats aged 6 and 24 months respectively. In comparison with the adult controls (6 months), in aged rats there was a decline in total aerobic NADH oxidation in both tissues; only minor (non-significant) changes, however, were found in NADH:coenzyme Q reductase and cytochrome oxidase activities, and there was no change in ubiquinol-cytochrome c reductase activity. The coenzyme Q levels were slightly decreased in mitochondria from both organs of aged rats. The lowered NADH oxidase activity is not due to the slight decrease observed in the coenzyme Q levels, but is the result of decreased Complex I activity. Since the assay of NADH:coenzyme Q reductase requires quinone analogues, none of which can evoke its maximal turnover [Estornell, Fato, Pallotti and Lenaz (1993) FEBS Lett. 332, 127-131], its activity has been calculated indirectly by taking advantage of the relationship that exists between NADH oxidation and ubiquinol oxidation through the coenzyme Q pool. The results, expressed in this way, show a drastic loss of activity of Complex I in both the heart and the liver of aged animals in comparison with adult controls.

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Year:  1995        PMID: 7575440      PMCID: PMC1136125          DOI: 10.1042/bj3110105

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  36 in total

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5.  Quantitative analysis of age-associated accumulation of mitochondrial DNA with deletion in human hearts.

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  13 in total

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Review 8.  Mitochondria-controlled signaling mechanisms of brain protection in hypoxia.

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9.  Molecular mechanism and physiological role of active-deactive transition of mitochondrial complex I.

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