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Effect of time of restriction on the decrease in mitochondrial H 2 O 2 production and oxidative DNA damage in the heart of food‐restricted rats
Author(s) -
Gredilla R.,
LópezTorres M.,
Barja G.
Publication year - 2002
Publication title -
microscopy research and technique
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 118
eISSN - 1097-0029
pISSN - 1059-910X
DOI - 10.1002/jemt.10204
Subject(s) - mitochondrial dna , caloric theory , oxidative damage , oxidative phosphorylation , mitochondrion , mitochondrial ros , biology , longevity , oxidative stress , chemistry , biochemistry , genetics , endocrinology , gene
In the present study, the question if medium‐term (4 months) caloric restriction (40%) decreases mitochondrial H 2 O 2 production and oxidative DNA damage was investigated. Caloric restriction (CR) is the only experimental manipulation that increases maximum life span. Previous long‐term CR studies have showed that CR decreases the mitochondrial rate of free radical production in diverse tissues and species. Those studies agree with the idea that the superior longevity of the restricted animals can be partly due to their lower mitochondrial rate of free radical generation. However, caloric restriction effects strongly depend on implementation time. Previous studies have shown that the decrease induced by CR on oxygen radical generation and oxidative damage to mitochondrial DNA occurs after 1 year but not after 6 weeks of restriction. In the present investigation, mitochondrial H 2 O 2 production did not change in medium‐term (4 months) caloric restricted animals, and, in agreement with that, no differences were found in either mitochondrial or nuclear oxidative DNA damage between restricted and ad libitum–fed animals. These results confirm the importance of the time of CR implementation, and show that time longer than 4 months is needed to decrease the mitochondrial rate of free radical generation and the oxidative damage to mtDNA in the rat heart. Microsc. Res. Tech. 59:273–277, 2002. © 2002 Wiley‐Liss, Inc.