Rationale for the existence of additional adipostatic hormones

被引:98
作者
Frühbeck, G
Gómez-Ambrosi, J
机构
[1] Univ Navarra Clin, Dept Endocrinol, Pamplona 31008, Spain
[2] Univ Navarra, Metab Res Lab, E-31080 Pamplona, Spain
关键词
leptin; parabiosis; lipostatic factor; obesity; energy balance;
D O I
10.1096/fj.00-0829hyp
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Parabiosis studies with obese rodents demonstrated that circulating factors are involved in the long-term control of food intake and energy balance. More than 40 years ago it was hypothesized that rats made obese by hypothalamic or dietary means, as well as genetically obese fa/fa rats and db/db mice, produce a circulating factor that either inhibits food intake or acts metabolically to reduce the fat content of non-obese ad libitum-fed partners. However, none of these obese rodents showed a significant change in weight when parabiosed to a normal animal. It was therefore postulated that these obese rodents produced a circulating lipostatic factor but were unable to respond to it. In contrast, genetically obese ob/ob mice were thought to be deficient in the circulating signal, as they lost weight when parabiosed to lean or obese db/db mice. The discovery of leptin suggested that the circulating lipostatic signal had been identified. However, a closer look at the outcome of the parabiotic studies reveals that leptin alone does not explain all of the findings of the parabiotic experiments. Another (or more than one) as yet unidentified factor(s) may be involved in energy balance regulation. The evidence for the existence of further leptin-like hormones comes from observations in which the direct effect of leptin has been eliminated or can be excluded.
引用
收藏
页码:1996 / 2006
页数:11
相关论文
共 72 条
[1]   Adipose-selective targeting of the GLUT4 gene impairs insulin action in muscle and liver [J].
Abel, ED ;
Peroni, O ;
Kim, JK ;
Kim, YB ;
Boss, O ;
Hadro, E ;
Minnemann, T ;
Shulman, GI ;
Kahn, BB .
NATURE, 2001, 409 (6821) :729-733
[2]  
Ailhaud G., 1998, HDB OBESITY, P359
[3]   Normal reproductive function in leptin-deficient patients with lipoatropic diabetes [J].
Andreelli, F ;
Hanaire-Broutin, H ;
Laville, M ;
Tauber, JP ;
Riou, JP ;
Thivolet, C .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (02) :715-719
[4]   Genetics of body-weight regulation [J].
Barsh, GS ;
Farooqi, IS ;
O'Rahilly, S .
NATURE, 2000, 404 (6778) :644-651
[5]   HYPOTHALAMIC AND GENETIC OBESITY IN EXPERIMENTAL-ANIMALS - AUTONOMIC AND ENDOCRINE HYPOTHESIS [J].
BRAY, GA ;
YORK, DA .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :719-809
[6]   RECOMBINANT MOUSE OB PROTEIN - EVIDENCE FOR A PERIPHERAL SIGNAL LINKING ADIPOSITY AND CENTRAL NEURAL NETWORKS [J].
CAMPFIELD, LA ;
SMITH, FJ ;
GUISEZ, Y ;
DEVOS, R ;
BURN, P .
SCIENCE, 1995, 269 (5223) :546-549
[7]   Correction of the sterility defect in homozygous obese female mice by treatment with the human recombinant leptin [J].
Chehab, FE ;
Lim, ME ;
Lu, RH .
NATURE GENETICS, 1996, 12 (03) :318-320
[8]   Early onset of reproductive function in normal female mice treated with leptin [J].
Chehab, FF ;
Mounzih, K ;
Lu, RH ;
Lim, ME .
SCIENCE, 1997, 275 (5296) :88-90
[9]   Leptin as a regulator of adipose mass and reproduction [J].
Chehab, FF .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2000, 21 (08) :309-314
[10]   Phenotypes of mouse diabetes and rat fatty due to mutations in the OB (leptin) receptor [J].
Chua, SC ;
Chung, WK ;
WuPeng, XS ;
Zhang, YY ;
Liu, SM ;
Tartaglia, L ;
Leibel, RL .
SCIENCE, 1996, 271 (5251) :994-996