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血管紧张素II和脱氧皮质酮输注对大鼠血管紧张素II受体的影响。

Effect of angiotensin II and deoxycorticosterone infusion on vascular angiotensin II receptors in rats.

作者信息

Schiffrin E L, Gutkowska J, Genest J

出版信息

Am J Physiol. 1984 Apr;246(4 Pt 2):H608-14. doi: 10.1152/ajpheart.1984.246.4.H608.

DOI:10.1152/ajpheart.1984.246.4.H608
PMID:6326599
Abstract

The effect of angiotensin II (ANG II) and deoxycorticosterone acetate (DOCA) on the density (Bmax) and affinity (Kd) of binding sites for 125I-ANG II was investigated in a particulate fraction prepared from rat mesenteric arteriolar arcades. Rats were infused with ANG II via Alzet osmotic minipumps at a dose of 200 ng X kg-1 X min-1 intraperitoneally or 60 and 200 ng X kg-1 X min-1 intravenously for 5 days. Bmax was 127 +/- 5 fmol/mg protein, and Kd was 0.8 +/- 0.1 nM in controls and was reduced significantly after the intraperitoneal infusion (111 +/- 10 fmol/mg) or the lower intravenous dose (111 +/- 9 fmol/mg), whereas after the higher intravenous dose Bmax did not change (144 +/- 14 fmol/mg). Kd was unaffected in all groups. Plasma renin activity (PRA) was reduced, and plasma ANG II increased in a dose-dependent fashion after ANG II infusion. Plasma aldosterone concentration increased only in the group infused with ANG II at 200 ng X kg-1 X min-1 intravenously (to 33.8 +/- 8.0 ng/dl from 11.6 +/- 3.4). In rats implanted subcutaneously with silicone rubber impregnated with DOCA, Bmax for 125I-ANG II was significantly increased (to 142 +/- 4 fmol/mg), whereas rats receiving 1% NaCl in their drinking water had no change in binding capacity, although PRA was lower in both groups. DOCA infusion, when combined with the intravenous dose of ANG II that reduced Bmax, antagonized this action of ANG II. DOCA infusion into sodium-depleted rats partially corrected the down-regulation of vascular ANG II receptors independent of changes in PRA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在从大鼠肠系膜小动脉弓制备的微粒部分中,研究了血管紧张素II(ANG II)和醋酸脱氧皮质酮(DOCA)对125I-ANG II结合位点密度(Bmax)和亲和力(Kd)的影响。大鼠通过Alzet渗透微型泵以200 ng·kg-1·min-1的剂量腹腔内注射ANG II,或以60和200 ng·kg-1·min-1的剂量静脉内注射5天。对照组中Bmax为127±5 fmol/mg蛋白,Kd为0.8±0.1 nM,腹腔内注射(111±10 fmol/mg)或较低静脉剂量(111±9 fmol/mg)后显著降低,而较高静脉剂量后Bmax未改变(144±14 fmol/mg)。所有组的Kd均未受影响。ANG II输注后,血浆肾素活性(PRA)降低,血浆ANG II呈剂量依赖性增加。仅在以200 ng·kg-1·min-1静脉内注射ANG II的组中,血浆醛固酮浓度增加(从11.6±3.4增至33.8±8.0 ng/dl)。皮下植入含DOCA硅橡胶的大鼠,125I-ANG II的Bmax显著增加(至142±4 fmol/mg),而饮用1% NaCl的大鼠结合能力无变化,尽管两组的PRA均较低。DOCA输注与降低Bmax的静脉剂量ANG II联合时,拮抗了ANG II的这一作用。向缺钠大鼠输注DOCA可部分纠正血管ANG II受体的下调,且与PRA变化无关。(摘要截短于250字)

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