Hanada R, Nakazato M, Matsukura S, Murakami N, Yoshimatsu H, Sakata T
Department of Internal Medicine I, School of Medicine, Oita Medical University, Oita, 879-5593, Japan.
Biochem Biophys Res Commun. 2000 Feb 5;268(1):88-91. doi: 10.1006/bbrc.1999.2081.
Agouti protein and agouti-related protein (AGRP) antagonize alpha-melanocyte-stimulating hormone that binds to and activates the melanocortin-4 receptor (MC4-R) in the hypothalamus, thereby stimulating food intake. Melanin-concentrating hormone (MCH) and orexin are orexigenic peptides that specifically are synthesized in the lateral hypothalamus. MCH gene expression was augmented in A(y)/a (agouti) mice which overexpress agouti protein, but orexin mRNA was not. AGRP administered intracerebroventricularly into wild-type rats augmented MCH but not orexin gene expression. Also, SHU9119, a peptidergic antagonist of MC4-R, increased only MCH mRNA. These findings indicate that interruption of signaling at MC4-R activates the MCH but not the orexin gene. The biosyntheses of MCH and orexin are regulated through different pathways.
刺鼠蛋白和刺鼠相关蛋白(AGRP)拮抗α-黑素细胞刺激素,α-黑素细胞刺激素与下丘脑的黑皮质素-4受体(MC4-R)结合并激活该受体,从而刺激食物摄入。黑色素浓缩激素(MCH)和食欲素是在下丘脑外侧特异性合成的促食欲肽。在过度表达刺鼠蛋白的A(y)/a(刺鼠)小鼠中,MCH基因表达增加,但食欲素mRNA未增加。向野生型大鼠脑室内注射AGRP可增加MCH但不增加食欲素基因表达。此外,MC4-R的肽能拮抗剂SHU9119仅增加MCH mRNA。这些发现表明,MC4-R信号的中断激活了MCH基因而非食欲素基因。MCH和食欲素的生物合成通过不同途径调节。