Negligible senescence in the longest living rodent, the naked mole-rat: insights from a successfully aging species

被引:339
作者
Buffenstein, Rochelle [1 ,2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Physiol, San Antonio, TX 78245 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Sam & Ann Barshop Inst Longev & Aging Studies, San Antonio, TX 78245 USA
来源
JOURNAL OF COMPARATIVE PHYSIOLOGY B-BIOCHEMICAL SYSTEMS AND ENVIRONMENTAL PHYSIOLOGY | 2008年 / 178卷 / 04期
关键词
slow aging; maximum lifespan; oxidative stress; reproduction; heterocephalus glaber;
D O I
10.1007/s00360-007-0237-5
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Aging refers to a gradual deterioration in function that, over time, leads to increased mortality risk, and declining fertility. This pervasive process occurs in almost all organisms, although some long-lived trees and cold water inhabitants reportedly show insignificant aging. Negligible senescence is characterized by attenuated age-related change in reproductive and physiological functions, as well as no observable age-related gradual increase in mortality rate. It was questioned whether the longest living rodent, the naked mole-rat, met these three strict criteria. Naked mole-rats live in captivity for more than 28.3 years, similar to 9 times longer than similar-sized mice. They maintain body composition from 2 to 24 years, and show only slight age-related changes in all physiological and morphological characteristics studied to date. Surprisingly breeding females show no decline in fertility even when well into their third decade of life. Moreover, these animals have never been observed to develop any spontaneous neoplasm. As such they do not show the typical age-associated acceleration in mortality risk that characterizes every other known mammalian species and may therefore be the first reported mammal showing negligible senescence over the majority of their long lifespan. Clearly physiological and biochemical processes in this species have evolved to dramatically extend healthy lifespan. The challenge that lies ahead is to understand what these mechanisms are.
引用
收藏
页码:439 / 445
页数:7
相关论文
共 42 条
[1]   Antioxidants do not explain the disparate longevity between mice and the longest-living rodent, the naked mole-rat [J].
Andziak, B ;
O'Connor, TP ;
Buffenstein, R .
MECHANISMS OF AGEING AND DEVELOPMENT, 2005, 126 (11) :1206-1212
[2]   Disparate patterns of age-related changes in lipid peroxidation in long-lived naked mole-rats and shorter-lived mice [J].
Andziak, Blazej ;
Buffenstein, Rochelle .
AGING CELL, 2006, 5 (06) :525-532
[3]   High oxidative damage levels in the longest-living rodent, the naked mole-rat [J].
Andziak, Blazej ;
O'Connor, Timothy P. ;
Qi, Wenbo ;
DeWaal, Eric M. ;
Pierce, Anson ;
Chaudhuri, Asish R. ;
Van Remmen, Holly ;
Buffenstein, Rochelle .
AGING CELL, 2006, 5 (06) :463-471
[4]   MAMMALIAN AGING, METABOLISM, AND ECOLOGY - EVIDENCE FROM THE BATS AND MARSUPIALS [J].
AUSTAD, SN ;
FISCHER, KE .
JOURNALS OF GERONTOLOGY, 1991, 46 (02) :B47-B53
[5]   An experimental paradigm for the study of slowly aging organisms [J].
Austad, SN .
EXPERIMENTAL GERONTOLOGY, 2001, 36 (4-6) :599-605
[6]  
Bennett N., 2000, AFRICAN MOLE RATS EC
[7]   The naked mole-rat? A new long-living model for human aging research [J].
Buffenstein, R .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2005, 60 (11) :1369-1377
[8]  
Buffenstein R, 2000, LIFE UNDERGROUND, P62
[9]  
BUFFENSTEIN R, 2002, NAKED MOLE RATE NEW
[10]  
Buffenstein R, 2007, FASEB J, V21, pA1423