Leptin - Much more than a satiety signal

被引:178
作者
Harris, RBS [1 ]
机构
[1] Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
关键词
insulin; reproduction; stress;
D O I
10.1146/annurev.nutr.20.1.45
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Much attention has focused on the effects of leptin as a central satiety agent. There is now a significant amount of evidence that leptin is active in the periphery. This review focuses on the ability of leptin to modify insulin sensitivity, tissue metabolism, stress responses, and reproductive function. Leptin's effect on several of these systems is mediated via the hypothalamic-pituitary axis. Therefore, although in vitro studies provide evidence for direct effects on specific tissues and metabolic pathways, it is essential to consider the interactions between leptin and other regulatory factors in vivo. Little is known about the regulation of peripheral receptor expression or the production of binding proteins. Both of these factors determine the bioactivity of circulating leptin and have the potential to induce a peripheral resistance to leptin, similar to the central "leptin resistance" observed in obese subjects. Future research will clarify which of the endocrine and metabolic actions of peripheral leptin are of physiological relevance and which should be considered a pharmacological manipulation.
引用
收藏
页码:45 / 75
页数:31
相关论文
共 246 条
[1]   Role of leptin in the neuroendocrine response to fasting [J].
Ahima, RS ;
Prabakaran, D ;
Mantzoros, C ;
Qu, DQ ;
Lowell, B ;
MaratosFlier, E ;
Flier, JS .
NATURE, 1996, 382 (6588) :250-252
[2]   Regulation of neuronal and glial proteins by leptin:: Implications for brain development [J].
Ahima, RS ;
Bjorbæk, C ;
Osei, S ;
Flier, JS .
ENDOCRINOLOGY, 1999, 140 (06) :2755-2762
[3]   Leptin -: A regulator of islet function?: Its plasma levels correlate with glucagon and insulin secretion in healthy women [J].
Ahrén, B ;
Larsson, H .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (12) :1477-1481
[4]   Changes in free insulin-like growth factor-1 and leptin concentrations during acute metabolic decompensation in insulin withdrawn patients with type 1 diabetes [J].
Attia, N ;
Caprio, S ;
Jones, TW ;
Heptulla, R ;
Holcombe, J ;
Silver, D ;
Sherwin, RS ;
Tamborlane, WV .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (07) :2324-2328
[5]   Metabolic control of sexual function and growth: Role of neuropeptide Y and leptin [J].
Aubert, ML ;
Pierroz, DD ;
Gruaz, NM ;
d'Alleves, V ;
Vuagnat, BAM ;
Pralong, FP ;
Blum, WF ;
Sizonenko, PC .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1998, 140 (1-2) :107-113
[6]   The stomach is a source of leptin [J].
Bado, A ;
Levasseur, S ;
Attoub, S ;
Kermorgant, S ;
Laigneau, JP ;
Bortoluzzi, MN ;
Moizo, L ;
Lehy, T ;
Guerre-Millo, M ;
Le Marchand-Brustel, Y ;
Lewin, MJM .
NATURE, 1998, 394 (6695) :790-793
[7]   Obese gene expression alters the ability of 30A5 preadipocytes to respond to lipogenic hormones [J].
Bai, YL ;
Zhang, SY ;
Kim, KS ;
Lee, JK ;
Kim, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (24) :13939-13942
[8]  
BARASH JA, 1996, ENDOCRINOLOGY, V137, P3144
[9]   Insulin stimulates both leptin secretion and production by rat white adipose tissue [J].
Barr, VA ;
Malide, D ;
Zarnowski, MJ ;
Taylor, SI ;
Cushman, SW .
ENDOCRINOLOGY, 1997, 138 (10) :4463-4472
[10]   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