© 2000 by European Society of Cardiology
Copyright © 2000, European Society of Cardiology
Aging is associated with increased lipid peroxidation in human hearts, but not with mitochondrial respiratory chain enzyme defects
aMuscle Research Unit, Department of Internal Medicine, Hospital Clìnic, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Villarroel 170, 08036 University of Barcelona, Barcelona, Catalonia, Spain
bClinical Biochemistry Laboratory, Hospital Clìnic, IDIBAPS, Barcelona, Catalonia, Spain
cUnité des Recherches sur les Handicaps Génétiques de l’Enfant, INSERM U393, Département de Pédiatrie, Hôpital des Enfants-Malades, Paris, France
* Corresponding author. Tel./fax: +34-93-227-5539 omiro{at}medicina.ub.es
Background: Aging is associated with increased oxidative damage at multiple cellular and tissular levels. A decrease in mitochondrial function has repeatedly been advocated as a primary key event, especially on the basis of analysis of skeletal muscle mitochondria. However, some doubts on this issue have arisen when confounding variables (such as physical activity or smoking habit) have been taken into account in the analysis of mitochondrial respiratory chain (MRC) enzyme activities or when additional analytical parameters such as enzyme ratios have been considered. Objective: To determine whether oxidative damage and enzyme activities of the MRC are influenced by the aging process in human hearts. Patients and methods: We studied cardiac muscle obtained from 59 organ donors (age: 56±12 years, 75% men). Oxidative membrane damage was evaluated through the assessment of lipid peroxidation. Absolute and relative enzyme activities (AEA and REA, respectively) of complex I, II, III and IV of the MRC were spectrophotometrically measured. Stoichiometric relationships among MRC complexes were also assessed through calculating MRC ratios. Linear regression analyses were employed to disclose any potential correlation between mitochondrial dysfunction and aging. Results: We found a progressive, significant increase of heart membrane lipid peroxidation with aging (P<0.05). Conversely, neither AEA nor REA decreased with age (P=n.s. for all complexes). Similarly to observations in other tissues, we found that stoichiometry of the MRC enzymes is maintained within a narrow range in human hearts. When the effects of aging on MRC ratios were explored, we failed again in demonstrating any subtle disarray. Conclusion: MRC enzymes remain preserved in heart with aging, and thus they cannot be considered the main cause of the increased oxidative damage associated with aging.
KEYWORDS Aging; Energy metabolism; Free radicals; Mitochondria; Oxidative phosphorylation
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