Reduced coenzyme Q10 supplementation decelerates senescence in SAMP1 mice
Reduced coenzyme Q10 supplementation decelerates senescence in SAMP1 mice
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DOI:
10.1016/j.exger.2005.11.007
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发表时间:
2006-02-01
影响因子:
3.9
通讯作者:
Higuchi, K
中科院分区:
文献类型:
--
作者:
Yan, J;Fujii, K;Higuchi, K
The SAMPI strain is a mouse model for accelerated senescence and severe senile amyloidosis. We determined whether supplementation with coenzyme Q10 (CoQ10) could decelerate aging in SAMP1 mice and its potential role in aging. Plasma concentrations of CoQ10 and CoQ9 decreased with age in SAMP1 but not in SAMR1 mice. Supplementation with reduced CoQ10 (CoQH(2), 250 mg/kg/day) for one week increased plasma CoQ10 concentrations, with an accompanying decrease in plasma CoQ9 concentrations. In two series of experiments, lifelong supplementation with CoQH2 decreased the senescence grading scores from 10 to 14 months, 7 to 15 months, and at 17 months of age. The body weight of female mice increased from 2 to 10 months of age versus controls in the second series of experiments. Lifelong CoQH2 supplementation did not prolong or shorten the lifespan, nor did it alter the murine senile amyloid (AApoAII) deposition rate or cancer incidence. In the second series of experiments, urinary levels of 8-hydroxydeoxyguanosine did not change with age or long-term supplementation with CoQH(2).Urinary levels of acrolein (ACR)-lysine adduct increased significantly with age in SAMPI mice; however, CoQH(2) had no effect. Thus, lifelong dietary supplementation with CoQH(2) decreased the degree of senescence in middle-aged SAMPI mice. (c) 2005 Elsevier Inc. All rights reserved.