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中枢降钙素基因相关肽(CGRP)受体在大鼠食物摄入控制中的生理作用证据。

Evidence for a physiological role of central calcitonin gene-related peptide (CGRP) receptors in the control of food intake in rats.

作者信息

Lutz T A, Rossi R, Althaus J, Del Prete E, Scharrer E

机构信息

Institute of Veterinary Physiology, University of Zuerich, Switzerland.

出版信息

Neurosci Lett. 1997 Jul 25;230(3):159-62. doi: 10.1016/s0304-3940(97)00503-x.

Abstract

In the present study, we investigated the role of central calcitonin gene-related peptide (CGRP) and amylin receptors in mediating the anorectic effects of CGRP and amylin in rats chronically cannulated in the lateral brain ventricle. Intracerebroventricular (ICV) injection of the CGRP and amylin receptor antagonist CGRP(8-37) failed to influence the anorectic effects of peripherally injected CGRP and amylin. CGRP(8-37) alone, however, increased food intake in food deprived rats when administered 2 h before food presentation. Under the same experimental conditions, the more specific amylin receptor antagonists amylin(8-37) or AC 187 did not affect food intake. We therefore conclude, that CGRP is a physiological regulator of food intake within the central nervous system, acting at central CGRP receptors. Peripheral receptors, however, are likely to mediate the anorectic effects of peripherally administered amylin and CGRP.

摘要

在本研究中,我们调查了中枢降钙素基因相关肽(CGRP)和胰淀素受体在介导CGRP和胰淀素对慢性经侧脑室插管大鼠的厌食作用中的作用。脑室内(ICV)注射CGRP和胰淀素受体拮抗剂CGRP(8-37)未能影响外周注射CGRP和胰淀素的厌食作用。然而,单独的CGRP(8-37)在给食前2小时给药时,会增加饥饿大鼠的食物摄入量。在相同的实验条件下,更具特异性的胰淀素受体拮抗剂胰淀素(8-37)或AC 187不影响食物摄入量。因此,我们得出结论,CGRP是中枢神经系统内食物摄入的生理调节因子,并作用于中枢CGRP受体。然而,外周受体可能介导外周给予的胰淀素和CGRP的厌食作用。

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