Angiotensin II receptor subtypes in rat renal preglomerular vessels.

Receptor Pub Date : 1992-01-01
H De León, R Garcia
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引用次数: 0

Abstract

A simple technique to isolate rat renal preglomerular vessels is described. Kidneys were pressed against a 0.3 mm stainless steel grid. The whole vascular tree, including the interlobar, arcuate, and interlobular arteries, as well as the afferent arterioles, remained on the grid surface from where they were recovered. Extensive washing yielded a highly pure preparation of renal microvessels. Radioligand binding experiments were performed to characterize 125I-[Sar1,Ile8]-ANG II binding sites in preglomerular microvessel membranes. Equilibrium saturation binding experiments revealed the presence of one group of high affinity receptors (Kd = 1.22 +/- 0.171 nM; Bmax = 209 +/- 14 fmol/mg protein). Competitive inhibition experiments with two highly specific nonpeptide ANG II antagonists, losartan (DuP 753), which is specific for the AT1 receptor subtype, and PD123319, which is specific for the AT2 subtype, demonstrated that the large majority of, if not all, ANG II receptors in rat renal preglomerular vessels correspond to the AT1 subtype.

大鼠肾肾小球前血管血管紧张素II受体亚型。
本文描述了一种分离大鼠肾小球前血管的简单方法。肾脏被压在0.3毫米的不锈钢网格上。整个血管树,包括叶间动脉、弓形动脉和小叶间动脉,以及传入小动脉,都保留在网格表面上。广泛的冲洗产生了高纯度的肾微血管制备。采用放射性配体结合实验表征肾小球前微血管膜上的125I-[Sar1,Ile8]- ang II结合位点。平衡饱和结合实验显示存在一组高亲和受体(Kd = 1.22 +/- 0.171 nM;Bmax = 209 +/- 14 fmol/mg蛋白)。两种高度特异性的非肽ANG II拮抗剂losartan (DuP 753)和PD123319 (AT2亚型)的竞争抑制实验表明,大鼠肾肾小球前血管中绝大多数(如果不是全部)ANG II受体对应于AT1亚型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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