Adiposity signaling and biological defense against weight gain: Absence of protection or central hormone resistance?

被引:66
作者
Schwartz, MW
Niswender, KD
机构
[1] Univ Washington, Harborview Med Ctr, Dept Med, Seattle, WA 98104 USA
[2] Vanderbilt Univ, Dept Med, Sch Med, Med Ctr, Nashville, TN 37232 USA
关键词
D O I
10.1210/jc.2004-0906
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An abundant and compelling literature supports the existence of a homeostatic system that dynamically adjusts energy intake and energy expenditure to promote stability of body fat mass. In the context of this system, the ease with which many individuals gain weight is difficult to explain. Some have argued that energy homeostasis operates primarily to defend against weight loss and that, over the course of evolution, biological defense against weight gain was not selected for. According to this Absence of Protection model, obesity is seen as the natural result of living in an obesigenic environment. An alternative hypothesis, termed the Central Resistance model, proposes that under normal circumstances, the energy homeostasis system provides an effective defense against weight gain as well as weight loss and that common forms of obesity involve genetic or acquired defects ( or interactions between them) that impair the function of this system. Here, we discuss these dichotomous possibilities within the context of current literature regarding energy homeostasis and suggest a strategy for distinguishing between them.
引用
收藏
页码:5889 / 5897
页数:9
相关论文
共 75 条
[1]   WEIGHT GAIN FROM SIMPLE OVEREATING .2. SERUM LIPIDS AND BLOOD VOLUME [J].
ANDERSON, JT ;
LAWLER, A ;
KEYS, A .
JOURNAL OF CLINICAL INVESTIGATION, 1957, 36 (01) :81-88
[2]   Short-term leptin-dependent inhibition of hepatic gluconeogenesis is mediated by insulin receptor substrate-2 [J].
Anderwald, C ;
Müller, G ;
Koca, G ;
Fürnsinn, C ;
Waldhäusl, W ;
Roden, M .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (07) :1612-1628
[3]   Leptin receptor signaling in is required for normal body POW neurons weight homeostasis [J].
Balthasar, N ;
Coppari, R ;
McMinn, J ;
Liu, SM ;
Lee, CE ;
Tang, V ;
Kenny, CD ;
McGovern, RA ;
Chua, SC ;
Elmquist, JK ;
Lowell, BB .
NEURON, 2004, 42 (06) :983-991
[4]   Activation of downstream signals by the long form of the leptin receptor [J].
Banks, AS ;
Davis, SM ;
Bates, SH ;
Myers, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (19) :14563-14572
[5]   STAT3 signalling is required for leptin regulation of energy balance but not reproduction [J].
Bates, SH ;
Stearns, WH ;
Dundon, TA ;
Schubert, M ;
Tso, AWK ;
Wang, YP ;
Banks, AS ;
Lavery, HJ ;
Haq, AK ;
Maratos-Flier, E ;
Neel, BG ;
Schwartz, MW ;
Myers, MG .
NATURE, 2003, 421 (6925) :856-859
[6]  
BERNSTEIN IL, 1975, P SOC EXP BIOL MED, V150, P546, DOI 10.3181/00379727-150-39075
[7]   Mind versus metabolism in the control of food intake and energy balance [J].
Berthoud, HR .
PHYSIOLOGY & BEHAVIOR, 2004, 81 (05) :781-793
[8]   The role of SOCS-3 in leptin signaling and leptin resistance [J].
Bjorbæk, C ;
El-Haschimi, K ;
Frantz, JD ;
Flier, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (42) :30059-30065
[9]   Bariatric surgery and long-term control of morbid obesity [J].
Brolin, RE .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (22) :2793-2796
[10]   Role of brain insulin receptor in control of body weight and reproduction [J].
Brüning, JC ;
Gautam, D ;
Burks, DJ ;
Gillette, J ;
Schubert, M ;
Orban, PC ;
Klein, R ;
Krone, W ;
Müller-Wieland, D ;
Kahn, CR .
SCIENCE, 2000, 289 (5487) :2122-2125