Aging is associated with resistance to effects of leptin on fat distribution and insulin action

被引:67
作者
Ma, XH
Muzumdar, R
Yang, XM
Gabriely, I
Berger, R
Barzilai, N
机构
[1] Albert Einstein Coll Med, Inst Aging Res, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Ctr Diabet Res & Training, Bronx, NY 10461 USA
[3] Childrens HOsp Montefiore, Div Pediat Endocrinol, Bronx, NY USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2002年 / 57卷 / 06期
关键词
D O I
10.1093/gerona/57.6.B225
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
Leptin has been shown to modulate total body fat and visceral fat distribution and to enhance insulin action in young rats. We hypothesize that failure of leptin action may contribute to the increase in visceral fat and insulin resistance in aging. By chronic subcutaneous infusion of leptin over 7 days, we increased leptin levels in young rats to match the levels in aging ad libitum fed rats. Leptin induced an similar to50% decrease in food intake compared with saline controls, an similar to50% decrease in visceral fat, and improved hepatic (fourfold) and peripheral (30%) insulin action (euglycemic hyperinsulinemic clamp technique) compared with the pair-fed group (p < .001). Although the plasma leptin level was doubled in aging rats, leptin failed to produce a significant change in food intake, in fat mass and its distribution, and in hepatic and peripheral insulin action. Increasing plasma leptin levels failed to suppress leptin gene expression in aging rats as compared with the similar to50% suppression seen in young rats (p < .01). We propose that leptin resistance may play a causative role in the metabolic decline seen with aging.
引用
收藏
页码:B225 / B231
页数:7
相关论文
共 43 条
[1]   Regulation of plasma leptin in mice: Influence of age, high-fat diet, and fasting [J].
Ahren, B ;
Mansson, S ;
Gingerich, RL ;
Havel, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 273 (01) :R113-R120
[2]   Body composition, visceral fat, leptin, and insulin resistance in Asian Indian men [J].
Banerji, MA ;
Faridi, N ;
Atluri, R ;
Chaiken, RL ;
Lebovitz, HE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (01) :137-144
[3]  
Barnes CA, 2001, INT REV NEUROBIOL, V45, P339
[4]   RELATIONSHIP BETWEEN CHANGES IN BODY-COMPOSITION AND INSULIN RESPONSIVENESS IN MODELS OF THE AGING RAT [J].
BARZILAI, N ;
ROSSETTI, L .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 269 (03) :E591-E597
[5]   Decreased visceral adiposity accounts for leptin effect on hepatic but not peripheral insulin action [J].
Barzilai, N ;
She, L ;
Liu, LS ;
Wang, JL ;
Hu, MZ ;
Vuguin, P ;
Rossetti, L .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 277 (02) :E291-E298
[6]   Leptin selectively decreases visceral adiposity and enhances insulin action [J].
Barzilai, N ;
Wang, JL ;
Massilon, D ;
Vuguin, P ;
Hawkins, M ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (12) :3105-3110
[7]   Caloric restriction reverses hepatic insulin resistance in aging rats by decreasing visceral fat [J].
Barzilai, N ;
Banerjee, S ;
Hawkins, M ;
Chen, W ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (07) :1353-1361
[8]   Surgical removal of visceral fat reverses hepatic insulin resistance [J].
Barzilai, N ;
She, L ;
Liu, BQ ;
Vuguin, P ;
Cohen, P ;
Wang, JL ;
Rossetti, L .
DIABETES, 1999, 48 (01) :94-98
[9]   Interaction between aging and Syndrome X: New insights on the pathophysiology of fat distribution [J].
Barzilai, N ;
Gupta, G .
THE METABOLIC SYNDROME X: CONVERGENCE OF INSULIN RESISTANCE, GLUCOSE INTOLERANCE, HYPERTENSION, OBESITY, AND DYSLIPIDEMIAS-SEARCHING FOR THE UNDERLYING DEFECTS, 1999, 892 :58-72
[10]   Serum leptin in elderly people: Associations with sex hormones, insulin, and adipose tissue volumes [J].
Baumgartner, RN ;
Ross, RR ;
Waters, DL ;
Brooks, WM ;
Morley, JE ;
Montoya, GD ;
Garry, PJ .
OBESITY RESEARCH, 1999, 7 (02) :141-149