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非洲爪蟾侧线器官中降钙素基因相关肽(CGRP)受体的药理学特性

Pharmacological characterization of the CGRP receptor in the lateral line organ of Xenopus laevis.

作者信息

Bailey G P, Sewell W F

机构信息

Eaton-Peabody Laboratory of Auditory Physiology, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA.

出版信息

J Assoc Res Otolaryngol. 2000 Aug;1(1):82-8. doi: 10.1007/s101620010007.

Abstract

Calcitonin gene-related peptide (CGRP) is a neurotransmitter candidate colocalized with acetylcholine in efferent fibers innervating hair cell organs. We have used the Xenopus laevis lateral line organ to investigate the responses of a hair cell organ to the CGRP family of peptides. Two isoforms of CGRP, r alpha-CGRP and r beta-CGRP, and a human analog of alpha-CGRP, h(Tyro) alpha-CGRP, produced dose-dependent increases in afferent nerve fiber discharge rate with EC50 values of approximately 1 microM. Rate increases were 31.2, 18.9, and 10.3%, respectively. The peptide fragment rCGRP8-37 a selective CGRP1 receptor antagonist, competitively inhibited the response to r alpha-CGRP. Diacetoamidomethyl cysteine CGRP (r[Cys(ACM)2,7]alpha-CGRP), a CGRP2 agonist, did not change discharge rate. Rat amylin did not increase rate until very high concentrations, and then the change was less than 7%. Rat adrenomedullin produced no increase in rate. Responses to r alpha-CGRP developed after metamorphosis. No change in spontaneous discharge rate was observed until postmetamorphic day 6, and then it was only a fraction of the maximal response. This response progressively increased until postmetamorphic day 28, when it reached its maximal value. The most straightforward interpretation of our results is that the effect of CGRP is mediated by the CGRP1 receptor and that CGRP, of the peptides presently known to exist in the CGRP family, is the most likely endogenous peptide mediating these effects.

摘要

降钙素基因相关肽(CGRP)是一种神经递质候选物,与乙酰胆碱共定位于支配毛细胞器官的传出纤维中。我们利用非洲爪蟾侧线器官来研究毛细胞器官对CGRP肽家族的反应。CGRP的两种同工型,rα-CGRP和rβ-CGRP,以及α-CGRP的一种人类类似物h(Tyro)α-CGRP,产生剂量依赖性的传入神经纤维放电率增加,EC50值约为1 microM。放电率增加分别为31.2%、18.9%和10.3%。肽片段rCGRP8-37(一种选择性CGRP1受体拮抗剂)竞争性抑制对rα-CGRP的反应。二乙酰氨基甲基半胱氨酸CGRP(r[Cys(ACM)2,7]α-CGRP),一种CGRP2激动剂,未改变放电率。大鼠胰淀素直到非常高的浓度才增加放电率,然后变化小于7%。大鼠肾上腺髓质素未使放电率增加。对rα-CGRP的反应在变态后出现。直到变态后第6天,自发放电率没有变化,然后它只是最大反应的一小部分。这种反应逐渐增加,直到变态后第28天达到最大值。我们结果最直接的解释是CGRP的作用是由CGRP1受体介导的,并且在目前已知存在于CGRP家族的肽中,CGRP是最可能介导这些作用的内源性肽。

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