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高血压大鼠脑中利钠肽的受体亚型

Receptor subtypes for natriuretic peptides in the brains of hypertensive rats.

作者信息

Brown J, Czarnecki A

机构信息

Physiological Laboratory, Cambridge, United Kingdom.

出版信息

Am J Physiol. 1991 Feb;260(2 Pt 2):R441-7. doi: 10.1152/ajpregu.1991.260.2.R441.

Abstract

Receptor subtypes for alpha-atrial natriuretic peptide (alpha-ANP) were characterized in brains of 12-wk-old Wistar-Kyoto (WKY) and spontaneously hypertensive rats (SHR) by in vitro autoradiography, using des[Gln18, Ser19,Gly20,Leu21,Gly22]ANP-(4-23) (C-ANP) and ANP-(5-25) as subtype-selective ligands. 125I-labeled alpha-ANP (200 pM) bound reversibly to arachnoid mater (AM), choroid plexus (ChP), subfornical organ (SFO), median preoptic nucleus, and supraoptic nucleus. Apparent Kd values for alpha-ANP in AM, ChP, and SFO were 1-6 nM and they were lowest in SHR. Maximal binding capacities for alpha-ANP on ChP and SFO were also significantly lower in SHR, and 10 microM C-ANP or 10 microM ANP-(5-25) inhibited most radioligand binding on AM of WKY and SHR. C-ANP significantly inhibited no other alpha-125I-ANP binding. ANP-(5-25) was a relatively weak inhibitor of alpha-125I-ANP binding to ChP and SFO in WKY but it was powerful in SHR. The results suggest that AM expresses clearance receptor for alpha-ANP in WKY and SHR. Other structures do not express this receptor significantly but express two other receptors for alpha-ANP, one mainly in WKY and one mainly in SHR.

摘要

通过体外放射自显影技术,使用去[Gln18, Ser19, Gly20, Leu21, Gly22]ANP-(4 - 23)(C - ANP)和ANP-(5 - 25)作为亚型选择性配体,对12周龄的Wistar - Kyoto(WKY)大鼠和自发性高血压大鼠(SHR)大脑中的α - 心房利钠肽(α - ANP)受体亚型进行了表征。125I标记的α - ANP(200 pM)可逆性结合蛛网膜(AM)、脉络丛(ChP)、穹窿下器官(SFO)、视前正中核和视上核。α - ANP在AM、ChP和SFO中的表观解离常数(Kd)值为1 - 6 nM,在SHR中最低。SHR中α - ANP在ChP和SFO上的最大结合容量也显著降低,10 μM C - ANP或10 μM ANP-(5 - 25)抑制了WKY和SHR的AM上的大多数放射性配体结合。C - ANP没有显著抑制其他α - 125I - ANP结合。ANP-(5 - 25)对WKY中α - 125I - ANP与ChP和SFO的结合是一种相对较弱的抑制剂,但在SHR中作用较强。结果表明,AM在WKY和SHR中表达α - ANP的清除受体。其他结构不显著表达这种受体,但表达另外两种α - ANP受体,一种主要在WKY中,另一种主要在SHR中。

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