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Stress resistance and aging: Influence of genes and nutrition
Previous studies have shown that dermal fibroblast cell lines derived from young adult mice of the long-lived Snell dwarf ( d w / d w ), Ames dwarf ( df/ df) and growth hormone receptor knockout (GHR-KO) mouse stocks are resistant, in vitro, to the cytotoxic effects of hydrogen peroxide, cadmium, ul...
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Published in: | Mechanisms of ageing and development 2006-08, Vol.127 (8), p.687-694 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Previous studies have shown that dermal fibroblast cell lines derived from young adult mice of the long-lived Snell dwarf (
d
w
/
d
w
), Ames dwarf (
df/
df) and growth hormone receptor knockout (GHR-KO) mouse stocks are resistant, in vitro, to the cytotoxic effects of hydrogen peroxide, cadmium, ultraviolet light, paraquat, and heat. Here we show that, in contrast, fibroblasts from mice on low-calorie (CR) or low methionine (Meth-R) diets are not stress resistant in culture, despite the longevity induced by both dietary regimes. A second approach, involving induction of liver cell death in live animals using acetaminophen (APAP), documented hepatotoxin resistance in the CR and Meth-R mice, but
d
w
/
d
w
and GHR-KO mutant mice were not resistant to this agent, and were in fact more susceptible than littermate controls to the toxic effects of APAP. These data thus suggest that while resistance to stress is a common characteristic of experimental life span extension in mice, the cell types showing resistance may differ among the various models of delayed or decelerated aging. |
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ISSN: | 0047-6374 1872-6216 |
DOI: | 10.1016/j.mad.2006.04.002 |