Deleterious consequences of antioxidant supplementation on lifespan in a wild-derived mammal
Author(s) -
Colin Selman,
Jane S. McLaren,
Andrew Collins,
Garry G. Duthie,
John R. Speakman
Publication year - 2013
Publication title -
biology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.596
H-Index - 110
eISSN - 1744-957X
pISSN - 1744-9561
DOI - 10.1098/rsbl.2013.0432
Subject(s) - biology , antioxidant , ageing , ascorbic acid , lipid peroxidation , oxidative damage , reactive oxygen species , oxidative stress , dna damage , oxidative phosphorylation , free radical theory of aging , microtus , vitamin , senescence , medicine , endocrinology , biochemistry , zoology , genetics , food science , dna
While oxidative damage owing to reactive oxygen species (ROS) often increases with advancing age and is associated with many age-related diseases, its causative role in ageing is controversial. In particular, studies that have attempted to modulate ROS-induced damage, either upwards or downwards, using antioxidant or genetic approaches, generally do not show a predictable effect on lifespan. Here, we investigated whether dietary supplementation with either vitamin E (α-tocopherol) or vitamin C (ascorbic acid) affected oxidative damage and lifespan in short-tailed field voles, Microtus agrestis . We predicted that antioxidant supplementation would reduce ROS-induced oxidative damage and increase lifespan relative to unsupplemented controls. Antioxidant supplementation for nine months reduced hepatic lipid peroxidation, but DNA oxidative damage to hepatocytes and lymphocytes was unaffected. Surprisingly, antioxidant supplementation significantly shortened lifespan in voles maintained under both cold (7 ± 2°C) and warm (22 ± 2°C) conditions. These data further question the predictions of free-radical theory of ageing and critically, given our previous research in mice, indicate that similar levels of antioxidants can induce widely different interspecific effects on lifespan.
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