Taylor G M, Meeran K, O'Shea D, Smith D M, Ghatei M A, Bloom S R
Division of Endocrinology and Metabolic Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, London, United Kingdom.
Endocrinology. 1996 Aug;137(8):3260-4. doi: 10.1210/endo.137.8.8754748.
The central effect of adrenomedullin on feeding was investigated in fasted rats. After intracerebroventricular administration, adrenomedullin decreased 2-h food intake in a dose-dependent manner. A dose of 1.7 nmol adrenomedullin decreased 2-h food intake by 57%. Adrenomedullin shares sequence homology with calcitonin gene-related peptide (CGRP), a central anorectic agent, and binding sites for both are present in the hypothalamus. Adrenomedullin competed for [125I]adrenomedullin- and [125I]CGRP-binding sites in hypothalamic membranes. The Kd for the [125I]adrenomedullin-binding site was 0.54 +/- 0.07 nM, with a binding capacity of 214 +/- 27 fmol/mg membrane protein (n = 3). CGRP and the CGRP receptor antagonist CGRP-(8-37) at concentrations up to 1 microM did not compete at these sites. The Kd for the CGRP-binding site was 0.10 +/- 0.02 nM, with a binding capacity of 250 +/- 31 fmol/mg, and the Ki values for adrenomedullin and CGRP-(8-37) were 4.6 +/- 2.1 and 4.0 +/- 1.6 nM, respectively (n = 3). Thus, adrenomedullin showed high affinity binding at both adrenomedullin- and CGRP-binding sites. To establish whether adrenomedullin reduces feeding via CGRP receptors, we coadministered adrenomedullin (1.7 nmol) and CGRP-(8-37) (30 nmol). The reduction in 2-h food intake induced by adrenomedullin was 50% inhibited by CGRP-(8-37). These results show that adrenomedullin decreases food intake in the rat, and this effect is mediated at least in part via CGRP receptors.
在禁食大鼠中研究了肾上腺髓质素对进食的中枢作用。脑室内给药后,肾上腺髓质素以剂量依赖性方式减少2小时食物摄入量。1.7 nmol剂量的肾上腺髓质素使2小时食物摄入量减少了57%。肾上腺髓质素与降钙素基因相关肽(CGRP,一种中枢性食欲抑制剂)具有序列同源性,且二者的结合位点均存在于下丘脑。肾上腺髓质素可竞争下丘脑膜中[125I]肾上腺髓质素和[125I]CGRP的结合位点。[125I]肾上腺髓质素结合位点的解离常数(Kd)为0.54±0.07 nM,结合容量为214±27 fmol/mg膜蛋白(n = 3)。浓度高达1μM的CGRP和CGRP受体拮抗剂CGRP-(8 - 37)在这些位点不产生竞争。CGRP结合位点的Kd为0.10±0.02 nM,结合容量为250±31 fmol/mg,肾上腺髓质素和CGRP-(8 - 37)的抑制常数(Ki)分别为4.6±2.1和4.0±1.6 nM(n = 3)。因此,肾上腺髓质素在肾上腺髓质素结合位点和CGRP结合位点均表现出高亲和力结合。为确定肾上腺髓质素是否通过CGRP受体减少进食,我们联合给予肾上腺髓质素(1.7 nmol)和CGRP-(8 - 37)(30 nmol)。CGRP-(8 - 37)可抑制肾上腺髓质素诱导的2小时食物摄入量减少的50%。这些结果表明,肾上腺髓质素可减少大鼠的食物摄入量,且这种作用至少部分是通过CGRP受体介导的。