Marsh D J, Hollopeter G, Huszar D, Laufer R, Yagaloff K A, Fisher S L, Burn P, Palmiter R D
Howard Hughes Medical Institute and Department of Biochemistry, University of Washington, Seattle 98195, USA.
Nat Genet. 1999 Jan;21(1):119-22. doi: 10.1038/5070.
Mutations reducing the functional activity of leptin, the leptin receptor, alpha-melanocyte stimulating hormones (alpha-MSH) and the melanocortin-4 receptor (Mc4r) all lead to obesity in mammals. Moreover, mutant mice that ectopically express either agouti (Ay/a mice) or agouti-related protein (Agrp), antagonists of melanocortin signalling, become obese. These data suggest that alpha-MSH signalling transduced by Mc4r tonically inhibits feeding; however, it is not known to what extent this pathway mediates leptin signalling. We show here that Mc4r-deficient (Mc4r-/-) mice do not respond to the anorectic actions of MTII, an MSH-like agonist, suggesting that alpha-MSH inhibits feeding primarily by activating Mc4r. Obese Mc4r-/-mice do not respond significantly to the inhibitory effects of leptin on feeding, whereas non-obese Mc4r-/- mice do. These data demonstrate that melanocortin signalling transduced by Mc4r is not an exclusive target of leptin action and that factors resulting from obesity contribute to leptin resistance. Leptin resistance of obese Mc4r-/- mice does not prevent their response to the anorectic actions of ciliary neurotrophic factor (CNTF), corticotropin releasing factor (CRF), or urocortin; or the orexigenic actions of neuropeptide Y (NPY) or peptide YY (PYY), indicating that these neuromodulators act independently or downstream of Mc4r signalling.
瘦素、瘦素受体、α-黑素细胞刺激激素(α-MSH)以及黑皮质素-4受体(Mc4r)功能活性降低的突变都会导致哺乳动物肥胖。此外,异位表达刺鼠信号蛋白(Ay/a小鼠)或刺鼠相关蛋白(Agrp,黑皮质素信号的拮抗剂)的突变小鼠也会肥胖。这些数据表明,由Mc4r转导的α-MSH信号持续抑制进食;然而,尚不清楚该途径在多大程度上介导瘦素信号。我们在此表明,Mc4r基因缺陷(Mc4r-/-)小鼠对MTII(一种MSH样激动剂)的厌食作用无反应,这表明α-MSH主要通过激活Mc4r来抑制进食。肥胖的Mc4r-/-小鼠对瘦素对进食的抑制作用无明显反应,而非肥胖的Mc4r-/-小鼠则有反应。这些数据表明,由Mc4r转导的黑皮质素信号不是瘦素作用的唯一靶点,肥胖导致的因素会导致瘦素抵抗。肥胖的Mc4r-/-小鼠的瘦素抵抗并不妨碍它们对睫状神经营养因子(CNTF)、促肾上腺皮质激素释放因子(CRF)或尿皮质素的厌食作用产生反应;也不妨碍它们对神经肽Y(NPY)或肽YY(PYY)的促食欲作用产生反应,这表明这些神经调节剂独立发挥作用或在Mc4r信号下游发挥作用。