The role of the central melanocortin system in the regulation of food intake and energy homeostasis: lessons from mouse models
A little more than a decade ago, the molecular basis of the lipostat was largely unknown. At that time, many laboratories were at work attempting to clone the genes encoding the obesity, diabetes, fatty, tubby and agouti loci, with the hope that identification of these obesity genes would help shed...
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Published in | Philosophical transactions of the Royal Society of London. Series B. Biological sciences Vol. 361; no. 1471; pp. 1265 - 1274 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
London
The Royal Society
29.07.2006
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Subjects | |
Online Access | Get full text |
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Summary: | A little more than a decade ago, the molecular basis of the lipostat was largely unknown. At that time, many laboratories were at work attempting to clone the genes encoding the obesity, diabetes, fatty, tubby and agouti loci, with the hope that identification of these obesity genes would help shed light on the process of energy homeostasis, appetite and energy expenditure. Characterization of obesity and diabetes elucidated the nature of the adipostatic hormone leptin and its receptor, respectively, while cloning of the agouti gene eventually led to the identification and characterization of one of the key neural systems upon which leptin acts to regulate intake and expenditure. In this review, we describe the neural circuitry known as the central melanocortin system and discuss the current understanding of its role in feeding and other processes involved in energy homeostasis. |
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Bibliography: | ArticleID:rstb20061861 istex:AD90DBCC10322DAFF017003E40A43538812EAA2E ark:/67375/V84-KBVXFDLD-N href:1265.pdf ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0962-8436 1471-2970 |
DOI: | 10.1098/rstb.2006.1861 |