PMID- 17652427 OWN - NLM STAT- MEDLINE DCOM- 20071213 LR - 20200930 IS - 0363-6143 (Print) IS - 0363-6143 (Linking) VI - 293 IP - 4 DP - 2007 Oct TI - Sexual dimorphism in liver mitochondrial oxidative capacity is conserved under caloric restriction conditions. PG - C1302-8 AB - Caloric restriction (CR) without malnutrition has been shown to increase maximal life span and delay the rate of aging in a wide range of species. It has been proposed that reduction in energy expenditure and oxidative damage may explain the life-extending effect of CR. Sex-related differences also have been shown to influence longevity and energy expenditure in many mammalian species. The aim of the present study was to determine the sex-related differences in rat liver mitochondrial machinery, bioenergetics, and oxidative balance in response to short-term CR. Mitochondria were isolated from 6-mo-old male and female Wistar rats fed ad libitum or subjected to 40% CR for 3 mo. Mitochondrial O(2) consumption, activities of the oxidative phosphorylation system (complexes I, III, IV, and V), antioxidative activities [MnSOD, glutathione peroxidase (GPx)], mitochondrial DNA and protein content, mitochondrial H(2)O(2) production, and markers of oxidative damage, as well as cytochrome C oxidase and mitochondrial transcription factor A levels, were measured. Female rats showed a higher oxidative capacity and GPx activity than males. This sexual dimorphism was not modified by CR. Restricted rats showed slightly increased oxygen consumption, complex III activity, and GPx antioxidant activity together with lower levels of oxidative damage. In conclusion, the sexual dimorphism in liver mitochondrial oxidative capacity was unaffected by CR, with females showing higher mitochondrial functionality and ROS protection than males. FAU - Valle, A AU - Valle A AD - Grup de Metabolisme Energetic i Nutricio, Departament de Biologia Fonamental i Ciencies de la Salut, Universitat de les Illes Balears, E-07122, Palma de Mallorca, Spain. FAU - Guevara, R AU - Guevara R FAU - Garcia-Palmer, F J AU - Garcia-Palmer FJ FAU - Roca, P AU - Roca P FAU - Oliver, J AU - Oliver J LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070725 PL - United States TA - Am J Physiol Cell Physiol JT - American journal of physiology. Cell physiology JID - 100901225 RN - 0 (DNA, Mitochondrial) RN - 0 (Mitochondrial Proteins) RN - 0 (Tfam protein, rat) RN - 0 (Thiobarbituric Acid Reactive Substances) RN - 0 (Transcription Factors) RN - BBX060AN9V (Hydrogen Peroxide) RN - EC 1.11.1.9 (Glutathione Peroxidase) RN - EC 1.15.1.1 (Superoxide Dismutase) RN - EC 1.9.3.- (cytochrome C oxidase subunit II) RN - EC 1.9.3.1 (Electron Transport Complex IV) RN - EC 7.1.1.2 (Electron Transport Complex I) RN - EC 7.1.1.8 (Electron Transport Complex III) SB - IM MH - Animals MH - Body Weight/physiology MH - *Caloric Restriction MH - DNA, Mitochondrial/analysis MH - Electron Transport Complex I/metabolism MH - Electron Transport Complex III/metabolism MH - Electron Transport Complex IV/analysis/metabolism MH - Female MH - Glutathione Peroxidase/metabolism MH - Hydrogen Peroxide/metabolism MH - Liver/anatomy & histology/chemistry/metabolism MH - Male MH - Mitochondria, Liver/chemistry/*metabolism MH - Mitochondrial Proteins/analysis/metabolism MH - Organ Size/physiology MH - *Oxidative Phosphorylation MH - Oxygen Consumption/physiology MH - Protein Carbonylation/physiology MH - Rats MH - Rats, Wistar MH - Sex Factors MH - Superoxide Dismutase/metabolism MH - Thiobarbituric Acid Reactive Substances/metabolism MH - Transcription Factors/analysis/metabolism EDAT- 2007/07/27 09:00 MHDA- 2007/12/14 09:00 CRDT- 2007/07/27 09:00 PHST- 2007/07/27 09:00 [pubmed] PHST- 2007/12/14 09:00 [medline] PHST- 2007/07/27 09:00 [entrez] AID - 00203.2007 [pii] AID - 10.1152/ajpcell.00203.2007 [doi] PST - ppublish SO - Am J Physiol Cell Physiol. 2007 Oct;293(4):C1302-8. doi: 10.1152/ajpcell.00203.2007. Epub 2007 Jul 25.