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降钙素基因相关肽受体拮抗剂人降钙素基因相关肽-(8-37)

Calcitonin gene-related peptide receptor antagonist human CGRP-(8-37).

作者信息

Chiba T, Yamaguchi A, Yamatani T, Nakamura A, Morishita T, Inui T, Fukase M, Noda T, Fujita T

机构信息

Third Department of Internal Medicine, Kobe University School of Medicine, Japan.

出版信息

Am J Physiol. 1989 Feb;256(2 Pt 1):E331-5. doi: 10.1152/ajpendo.1989.256.2.E331.

Abstract

From this study, we predicted that the human calcitonin gene-related peptide (hCGRP) fragment hCGRP-(8-37) would be a selective antagonist for CGRP receptors but an agonist for calcitonin (CT) receptors. In rat liver plasma membrane, where CGRP receptors predominate and CT appears to act through these receptors, hCGRP-(8-37) dose dependently displaced 125I-[Tyr0]rat CGRP binding. However, hCGRP-(8-37) had no effect on adenylate cyclase activity in liver plasma membrane. Furthermore, hCGRP-(8-37) inhibited adenylate cyclase activation induced not only by hCGRP but also by hCT. On the other hand, in LLC-PK1 cells, where calcitonin receptors are abundant and CGRP appears to act via these receptors, the bindings of 125I-[Tyr0]rat CGRP and 125I-hCT were both inhibited by hCGRP-(8-37). In contrast to liver membranes, interaction of hCGRP-(8-37) with these receptors led to stimulation of adenosine 3',5'-cyclic monophosphate (cAMP) production in LLC-PK1 cells, and moreover, this fragment did not inhibit the increased production of cAMP induced not only by hCT but also by hCGRP. Thus hCGRP-(8-37) appears to be a useful tool for determining whether the action of CGRP as well as that of CT is mediated via specific CGRP receptors or CT receptors.

摘要

通过本研究,我们预测人降钙素基因相关肽(hCGRP)片段hCGRP-(8 - 37)对CGRP受体而言是一种选择性拮抗剂,但对降钙素(CT)受体却是一种激动剂。在大鼠肝细胞膜中,CGRP受体占主导地位,且CT似乎通过这些受体发挥作用,hCGRP-(8 - 37)能剂量依赖性地取代125I-[酪氨酸0]大鼠CGRP的结合。然而,hCGRP-(8 - 37)对肝细胞膜中的腺苷酸环化酶活性没有影响。此外,hCGRP-(8 - 37)不仅抑制由hCGRP诱导的腺苷酸环化酶激活,还抑制由hCT诱导的腺苷酸环化酶激活。另一方面,在LLC-PK1细胞中,降钙素受体丰富,且CGRP似乎通过这些受体发挥作用,125I-[酪氨酸0]大鼠CGRP和125I-hCT的结合均被hCGRP-(8 - 37)抑制。与肝细胞膜不同,hCGRP-(8 - 37)与这些受体的相互作用导致LLC-PK1细胞中3',5'-环磷酸腺苷(cAMP)生成增加,而且,该片段并不抑制不仅由hCT而且由hCGRP诱导的cAMP生成增加。因此,hCGRP-(8 - 37)似乎是一种用于确定CGRP以及CT的作用是否通过特定的CGRP受体或CT受体介导的有用工具。

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