Longevity and the genetic determination of collagen glycoxidation kinetics in mammalian senescence

被引:172
作者
Sell, DR
Lane, MA
Johnson, WA
Masoro, EJ
Mock, OB
Reiser, KM
Fogarty, JF
Cutler, RG
Ingram, DK
Roth, GS
Monnier, VM
机构
[1] NIA, GERONTOL RES CTR, BALTIMORE, MD 21224 USA
[2] US FDA, DEPT HLTH & HUMAN SERV, LAUREL, MD 20708 USA
[3] UNIV TEXAS, HLTH SCI CTR, DEPT PHYSIOL, SAN ANTONIO, TX 78284 USA
[4] KIRKSVILLE COLL OSTEOPATH MED, DEPT ANAT, KIRKSVILLE, MO 63501 USA
[5] UNIV CALIF DAVIS, CALIF REG PRIMATE RES CTR, DAVIS, CA 95616 USA
关键词
life-span; oxidation; glycation; Maillard reaction; skin;
D O I
10.1073/pnas.93.1.485
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A fundamental question in the basic biology of aging is whether there is a universal aging process. If indeed such a process exists, one would expect that it develops at a higher rate in short- versus long-lived species, We have quantitated pentosidine, a marker of glycoxidative stress in skin collagen from eight mammalian species as a function of age. A curvilinear increase was modeled for all species, and the rate of increase correlated inversely with maximum life-span. Dietary restriction, a potent intervention associated with increased life-span, markedly inhibited glycoxidation rate in the rodent. On the assumption that collagen turnover rate is primarily influenced by the crosslinking due to glycoxidation, these results suggest that there is a progressive age-related deterioration of the process that controls the collagen glycoxidation rate, Thus, the ability to withstand damage due to glycoxidation and the Maillard reaction may be under genetic control.
引用
收藏
页码:485 / 490
页数:6
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