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[G调节蛋白在心脏血管紧张素II受体细胞内机制中的作用]

[The role of G-regulatory proteins in the intracellular mechanism of cardiac angiotensin-II receptors].

作者信息

Sechi L A, Sechi G, De Carli S, Griffin C A, Schambelan M, Bartoli E

机构信息

Centro Ipertensione, Università degli Studi, Udine.

出版信息

Cardiologia. 1993 Aug;38(8):519-23.

PMID:8313407
Abstract

High-affinity angiotensin II receptors have been identified in cardiac tissue of many animal species. In the heart, angiotensin II exerts positive inotropic and chronotropic effects, constricts coronary vessels, and stimulates cell growth. In vascular smooth muscle and adrenal cortex angiotensin II interacts with guanidine nucleotide regulatory proteins because GTP-gamma-S causes dissociation of the radioligand from its receptor. To investigate whether angiotensin II interacts with guanidine nucleotide regulatory proteins also in cardiac tissue, we studied the effects of GTP-gamma-S on [Sar1, Ile8]-angiotensin II binding to angiotensin II receptor subtypes (AT1 and AT2) in hearts obtained from 16- to 20-week-old Sprague-Dawley rats. We employed an in situ technique performed on frozen tissue sections. Competition experiments performed with the nonpeptide inhibitors losartan and PD123177 allowed identification of both AT1 and AT2 angiotensin II receptors in rat heart. These receptors were present in comparable amounts. In a different set of experiments the effects of GTP-gamma-S (100 microM) on radioligand displacement from AT1 and AT2 receptors were studied. GTP-gamma-S caused a progressive dissociation of the radioligand from the AT1 receptor indicating that this receptor interacts with guanidine nucleotide regulatory proteins. In contrast, the AT2 receptor does not appear to directly interact with guanidine nucleotide regulatory proteins. In summary, the study shows that both angiotensin II receptor subtypes are present in rat heart and that guanidine nucleotide regulatory proteins are implicated in the signal transduction mechanism of the cardiac AT1 receptor.

摘要

在许多动物物种的心脏组织中已鉴定出高亲和力的血管紧张素II受体。在心脏中,血管紧张素II具有正性肌力和变时作用,可收缩冠状血管,并刺激细胞生长。在血管平滑肌和肾上腺皮质中,血管紧张素II与鸟苷酸调节蛋白相互作用,因为GTP-γ-S会导致放射性配体与其受体解离。为了研究血管紧张素II在心脏组织中是否也与鸟苷酸调节蛋白相互作用,我们研究了GTP-γ-S对[Sar1,Ile8]-血管紧张素II与16至20周龄Sprague-Dawley大鼠心脏中血管紧张素II受体亚型(AT1和AT2)结合的影响。我们采用了对冷冻组织切片进行的原位技术。用非肽类抑制剂氯沙坦和PD123177进行的竞争实验能够鉴定大鼠心脏中的AT1和AT2血管紧张素II受体。这些受体的含量相当。在另一组实验中,研究了GTP-γ-S(100μM)对AT1和AT2受体放射性配体置换的影响。GTP-γ-S导致放射性配体从AT1受体逐渐解离,表明该受体与鸟苷酸调节蛋白相互作用。相比之下,AT2受体似乎不直接与鸟苷酸调节蛋白相互作用。总之该研究表明大鼠心脏中存在两种血管紧张素II受体亚型,并且鸟苷酸调节蛋白参与心脏AT1受体的信号转导机制。

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Cardiologia. 1993 Aug;38(8):519-23.
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