Weight regulation, leptin and growth hormone

被引:64
作者
Considine, RV [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46202 USA
关键词
leptin; ob gene; obesity; growth hormone;
D O I
10.1159/000191340
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Leptin, the product of the adipose tissue-specific ob gene, is a newly recognized hormone involved in the regulation of metabolism and body composition. Leptin appears to provide information to the central nervous system on the amount of energy stored in the adipose tissue. Serum leptin levels are highly correlated with body fat mass in adults, children and newborns. Obese individuals have significantly higher circulating leptin than normal, lean subjects. In addition, females have higher serum leptin than males with equivalent fat mass, Although leptin correlates with fat mass, circulating concentrations are altered by extremes in energy intake, such as fasting and overfeeding, Defects in leptin or its receptor in the hypothalamus lead to the development of obesity in several rodent models; however, no such deleterious defects have been identified in humans to date, Taken together, these observations suggest that humans may be resistant to their endogenous leptin levels. Despite this, studies in rodents demonstrating that leptin administration can cause weight loss in both ob/ob mice, and in normal weight controls suggest that leptin may be useful in the treatment of human obesity, This review will summarize the current understanding of leptin and its role in the regulation of body composition. In addition, the interaction of leptin with other metabolic hormones including growth hormone will be discussed.
引用
收藏
页码:116 / 121
页数:6
相关论文
共 57 条
[51]   Plasma leptin is partly cleared by the kidney and is elevated in hemodialysis patients [J].
Sharma, K ;
Considine, RV ;
Michael, B ;
Dunn, SR ;
Weisberg, LS ;
Kurnik, BRC ;
Kurnik, PB ;
OConnor, J ;
Sinha, M ;
Caro, JF .
KIDNEY INTERNATIONAL, 1997, 51 (06) :1980-1985
[52]   THE ROLE OF NEUROPEPTIDE-Y IN THE ANTIOBESITY ACTION OF THE OBESE GENE-PRODUCT [J].
STEPHENS, TW ;
BASINSKI, M ;
BRISTOW, PK ;
BUEVALLESKEY, JM ;
BURGETT, SG ;
CRAFT, L ;
HALE, J ;
HOFFMANN, J ;
HSIUNG, HM ;
KRIAUCIUNAS, A ;
MACKELLAR, W ;
ROSTECK, PR ;
SCHONER, B ;
SMITH, D ;
TINSLEY, FC ;
ZHANG, XY ;
HEIMAN, M .
NATURE, 1995, 377 (6549) :530-532
[53]   Identification and expression cloning of a leptin receptor, OB-R [J].
Tartaglia, LA ;
Dembski, M ;
Weng, X ;
Deng, NH ;
Culpepper, J ;
Devos, R ;
Richards, GJ ;
Campfield, LA ;
Clark, FT ;
Deeds, J ;
Muir, C ;
Sanker, S ;
Moriarty, A ;
Moore, KJ ;
Smutko, JS ;
Mays, GG ;
Woolf, EA ;
Monroe, CA ;
Tepper, RI .
CELL, 1995, 83 (07) :1263-1271
[54]   APPETITE AND THE REGULATION OF BODY-COMPOSITION [J].
WEIGLE, DS .
FASEB JOURNAL, 1994, 8 (03) :302-310
[55]   RECOMBINANT OB PROTEIN REDUCES FEEDING AND BODY-WEIGHT IN THE OB/OB MOUSE [J].
WEIGLE, DS ;
BUKOWSKI, TR ;
FOSTER, DC ;
HOLDERMAN, S ;
KRAMER, JM ;
LASSER, G ;
LOFTONDAY, CE ;
PRUNKARD, DE ;
RAYMOND, C ;
KUIJPER, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (04) :2065-2070
[56]  
WING RR, 1996, HORM METAB RES, V12, P698
[57]   POSITIONAL CLONING OF THE MOUSE OBESE GENE AND ITS HUMAN HOMOLOG [J].
ZHANG, YY ;
PROENCA, R ;
MAFFEI, M ;
BARONE, M ;
LEOPOLD, L ;
FRIEDMAN, JM .
NATURE, 1994, 372 (6505) :425-432