Krebs cycle enzymes from livers of old mice are differentially regulated by caloric restriction

被引:27
作者
Kevork, HA
Ramsey, JJ
Weindruch, R
机构
[1] Univ Calif Davis, Dept Mol Biosci, Sch Vet Med, Davis, CA 95616 USA
[2] Univ Wisconsin, Sch Med, Dept Med, Madison, WI 53706 USA
[3] William S Middleton Mem Vet Adm Med Ctr, Geriatr Res Educ & Clin Ctr, Madison, WI 53705 USA
[4] Univ Wisconsin, Wisconsin Reg Primate Res Ctr, Madison, WI 53715 USA
关键词
caloric restriction; Krebs cycle enzymes; liver; aging;
D O I
10.1016/j.exger.2004.04.009
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Krebs cycle enzyme activities and levels of five metabolites were determined from livers of old mice (30 months) maintained either on control or on long-term caloric restriction (CR) diets (28 months). In CR mice, the cycle was divided into two major blocks, the first containing citrate synthase, aconitase and NAD-dependent isocitrate dehydrogenase which showed decreased activities, while the second block, containing the remaining enzymes, displayed increased activity (except for fumarase, which was unchanged). CR also resulted in decreased levels of citrate, glutamate and alpha-ketoglutarate, increased levels of malate, and unchanged levels of aspartate. The alpha-ketoglutarate/glutamate and malate/alpha-ketoglutarate ratios were higher in CR, in parallel with previously reported increases with CR in pyruvate carboxylase activity and glucagon levels, respectively. The results indicate that long-term CR induces a differential regulation of Krebs cycle in old mice and this regulation may be the result of changes in gene expression levels, as well as a complex interplay between enzymes. hormones and other effectors. Truncation of Krebs cycle by CR may be an important adaptation to utilize available substrates for the gluconeogenesis necessary to sustain glycolytic tissues, such as brain. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1145 / 1154
页数:10
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