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大鼠肝细胞膜上降钙素基因相关肽的受体

Receptors for calcitonin gene-related peptide on the rat liver plasma membranes.

作者信息

Yamaguchi A, Chiba T, Okimura Y, Yamatani T, Morishita T, Nakamura A, Inui T, Noda T, Fujita T

机构信息

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

出版信息

Biochem Biophys Res Commun. 1988 Apr 15;152(1):383-91. doi: 10.1016/s0006-291x(88)80725-3.

Abstract

Specific binding sites for calcitonin gene-related peptide (CGRP) were identified in the rat liver plasma membrane. The binding of 125I-[TyrO]rat CGRP to rat liver plasma membrane was time dependent, saturable and reversible. Scatchard analysis of the data revealed a single class of binding sites with apparent dissociation constant of 260.8 pM and a maximal binding capacity of 26.6 fmol/mg of protein. Rat, chick, and human CGRP and their synthetic analogues inhibited label binding in a dose-dependent manner with relative potencies as follows; chick greater than rat greater than human greater than [TyrO]rat CGRP. Salmon, human and [Asu1'7]eel calcitonin also inhibited label binding but only at higher concentrations. These results clearly indicate the presence of specific binding sites for CGRP in rat liver plasma membrane and suggest that CGRP has possible biological actions on the rat liver.

摘要

在大鼠肝细胞膜中鉴定出降钙素基因相关肽(CGRP)的特异性结合位点。125I-[酪氨酸O]大鼠CGRP与大鼠肝细胞膜的结合具有时间依赖性、饱和性和可逆性。对数据进行Scatchard分析显示存在一类结合位点,其表观解离常数为260.8 pM,最大结合容量为26.6 fmol/mg蛋白质。大鼠、鸡和人CGRP及其合成类似物以剂量依赖性方式抑制标记物结合,相对效力如下:鸡>大鼠>人>[酪氨酸O]大鼠CGRP。鲑鱼降钙素、人降钙素和[1-7位为天冬氨酸]鳗鱼降钙素也抑制标记物结合,但仅在较高浓度时。这些结果清楚地表明大鼠肝细胞膜中存在CGRP的特异性结合位点,并提示CGRP对大鼠肝脏可能具有生物学作用。

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