The retardation of aging by caloric restriction: its significance in the transgenic era

被引:120
作者
Barger, JL
Walford, RL
Weindruch, R
机构
[1] Univ Wisconsin, William S Middleton Mem Vet Hosp, Ctr Geriatr Res Educ & Clin, Madison, WI 53705 USA
[2] Univ Wisconsin, Wisconsin Reg Primate Res Ctr, Madison, WI 53705 USA
[3] Univ Wisconsin, Sch Med, Dept Med, Madison, WI 53705 USA
[4] Univ Calif Los Angeles, Sch Med, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
aging; dwarf mice; insulin-like growth factor-1; growth hormone; transgenic mice;
D O I
10.1016/j.exger.2003.10.017
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
The retardation of aging and diseases by caloric restriction (CR) is a widely-studied and robust phenomenon. Recent publications describe transgenic and other mutant rodents displaying lifespan extension, and the rapid pace at which these animals are being generated raises the possibility that the importance of the CR paradigm is declining. Here we discuss these models and evaluate the evidence whether or not the aging process is retarded based on longevity, disease patterns and age-associated biological changes. A comparison to rodents on CR is made. Because CR has been investigated for similar to70 years with increasing intensity, there exists extensive data to document aging retardation. In contrast, for nearly all of the genetically abnormal models of lifespan extension, such data are minimal and often unconvincing; additional studies will be required to validate these strains as suitable models for aging research. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1343 / 1351
页数:9
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