Targeting tissue-specific metabolic signaling pathways in aging: the promise and limitations

被引:28
作者
Hu, Fang [1 ]
Liu, Feng [1 ]
机构
[1] Cent South Univ, Metab Syndrome Res Ctr, Xiangya Hosp 2, Changsha 410011, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
aging; metabolic disease; insulin; mTOR; caloric restriction; ENDOPLASMIC-RETICULUM STRESS; CHRONOLOGICAL LIFE-SPAN; UNFOLDED PROTEIN RESPONSE; AGE-RELATED DECLINE; RICH AKT SUBSTRATE; GROWTH-FACTOR-I; 40 KDA PRAS40; ER STRESS; MITOCHONDRIAL DYSFUNCTION; OXIDATIVE STRESS;
D O I
10.1007/s13238-013-0002-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been well established that most of the age-related diseases such as insulin resistance, type 2 diabetes, hypertension, cardiovascular disease, osteoporosis, and atherosclerosis are all closely related to metabolic dysfunction. On the other hand, interventions on metabolism such as calorie restriction or genetic manipulations of key metabolic signaling pathways such as the insulin and mTOR signaling pathways slow down the aging process and improve healthy aging. These findings raise an important question as to whether improving energy homeostasis by targeting certain metabolic signaling pathways in specific tissues could be an effective anti-aging strategy. With a more comprehensive understanding of the tissue-specific roles of distinct metabolic signaling pathways controlling energy homeostasis and the cross-talks between these pathways during aging may lead to the development of more effective therapeutic interventions not only for metabolic dysfunction but also for aging.
引用
收藏
页码:21 / 35
页数:15
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