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The leptin-dependent and –independent melanocortin signaling system: regulation of feeding and energy expenditure

Shimizu H, Inoue K, Mori M2007Journal of EndocrinologyReview
10.1677/joe-06-0144PubMedFree full text
Endocrine (ADH/ACTH/MSH)Hypothalamic-Pituitary

Abstract

The brain hypothalamus coordinates extra-hypothalamic regions to maintain energy homeostasis through the regulation of food intake and energy expenditure. A number of anorexigenic and orexigenic molecules in the hypothalamic nuclei participate in the control of energy homeostasis. Leptin and pro-opiomelanocortin (POMC)-derived α-melanocyte-stimulating hormone are key anorectic molecules, and the leptin receptor and POMC gene are both expressed in the hypothalamic arcuate nucleus. Although it has been considered that melanocortin signaling is localized downstream to leptin signaling, data have accumulated to support the concept of a leptin-independent melanocortin signaling system. We focus on and review the melanocortin signaling system that functions dependently or independently of leptin signaling in the regulation of energy homeostasis.

Cited By (1)

  • The tissue-specific processing of pro-opiomelanocortinJournal of Neuroendocrinology · 2008

References (3)

  • Targeted disruption of the melanocortin-4 receptor results in obesity in miceCell · 1997
  • Peripherally administered [Nle4,d-Phe7]-α-melanocyte stimulating hormone increases resting metabolic rate, while peripheral agouti-related protein has no effect, in wild type C57BL/6 and ob/ob miceJournal of Molecular Endocrinology · 2004
  • AgRP(83-132) Acts as an Inverse Agonist on the Human-Melanocortin-4 ReceptorMolecular Endocrinology · 2001

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