Melanocortin-4 receptor: A novel signalling pathway involved in body weight regulation

被引:23
作者
Fisher S.L. [1 ,2 ]
Yagaloff K.A. [1 ]
Burn P. [1 ]
机构
[1] Department of Metabolic Diseases, Hoffmann LaRoche, Nutley, NJ
[2] Biochemistry Dept, Astra Research Center, Boston, Cambridge, MA
关键词
Agouti; Diabetes; Leptin; Melanocortin; Ob; Obesity; POMC;
D O I
10.1038/sj.ijo.0800796
中图分类号
学科分类号
摘要
For many years, genetically obese mouse strains have provided models for human obesity. The Avy/-agouti mouse, one of the oldest obese mouse models, is characterized by maturity-onset obesity and diabetes as a result of ectopic expression of the secreted protein hormone, agouti protein. Agouti protein is normally expressed in hair follicles to regulate pigmentation through antagonism of the melanocortin-1 receptor, butin-vitrostudies have demonstrated that the hormone also has potent antagonist activity for the melanocortin-4 receptor (MC4-R). Subsequent development of the MC4-R knockout mouse model demonstrated that MC4-R plays a role in weight homeostasis as these mice recapitulated the metabolic defects of the agouti mouse. Further evidence for this hypothesis was obtained from pharmacological studies utilizing peptides with MC4-R agonist activity, that inhibitied food intake (when administered intracerebrally). Additional studies with peptide antagonists have now implicated the MC4-R in the leptin signalling pathway. Finally, evidence that the MC4-R may play a role in human obesity has been obtained from the identification of a dis-functional variant of the receptor in genetically obese subjects. © 1999 Stockton Press. All rights reserved.
引用
收藏
页码:54 / 58
页数:4
相关论文
共 37 条
[1]  
Parker S., Obesity: Trends and treatments. In: Scrip reports, PJB Publications Surrey 1996, pp. 6-15
[2]  
Jung R.T., Obesity as a disease, Br Med Bull, 53, pp. 307-321, (1997)
[3]  
Pi-Sunyer F.X., Medical hazards of obesity, Ann Intern Med, 119, pp. 655-660, (1993)
[4]  
Bouchard C., Perusse L., Genetics of obesity, Annu Rev Nutr, 13, pp. 337-354, (1993)
[5]  
Zhang Y., Proenca R., Maffei M., Barone M., Leopold L., Freidman J.M., Positional cloning of the mouse obese gene and its human homologue, Nature, 372, pp. 425-431, (1994)
[6]  
Campfield L.A., Smith F.J., Guisez Y., Devos R., Burn P., Recombinant mouse ob protein: Evidence for a peripheral signal linking adiposity and central neural networks, Science, 269, pp. 546-549, (1995)
[7]  
Campfield L.A., Smith F.J., Burn P., Ob protein: A hormonal controller of central neural networks mediating behavioral, metabolic, and neuroendocrine responses, Endocrin Metab, 4, pp. 81-102, (1997)
[8]  
Campfield L.A., Smith F.J., Burn P., The ob protein (Leptin) pathway-a link between adipose tissue mass and central neural networks, Horm Metab Res, 28, pp. 619-632, (1996)
[9]  
Campfield L.A., Smith F.J., Burn P., Strategies and potential molecular targets for obesity treatment, Science, 280, pp. 1383-1387, (1998)
[10]  
Woods S.C., Seeley R.J., Porte D., Schwartz M.W., Signals that regulate food intake and energy homeostasis, Science, 280, pp. 1378-1382, (1998)