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腺苷受体激动剂的肾血管效应。

Renovascular effects of adenosine receptor agonists.

作者信息

Holz F G, Steinhausen M

机构信息

I. Physiologisches Institut, Universität Heidelberg, BRD.

出版信息

Ren Physiol. 1987;10(5):272-82. doi: 10.1159/000173135.

Abstract

The purpose of the present experiments was to determine the renovascular effects of the adenosine agonists N-ethyl-carboxamide adenosine (NECA), N6-cyclohexyl adenosine (CHA) and 2-chloro adenosine (2-CLA). The diameter of pre- and postglomerular vessels in the split hydronephrotic kidney of Inactin-anesthetized rats was measured by in vivo television microscopy. All metabolically stable adenosine agonists were topically applied into the renal tissue bath. NECA, a preferential A2 adenosine receptor agonist, induced dose-dependent marked pre- and slight postglomerular vasodilation except for a small constrictory effect on the afferent arteriole near the glomerulus. Application of CHA, a selective A1 adenosine receptor agonist, led to a vasoconstriction of all preglomerular vessels, the extent of which was greatest at the most distal segment of the afferent arteriole. 2-CLA, a nonselective agonist, produced a small decrease in diameter in all preglomerular vessels, a marked constriction of the afferent arteriole at sites near the glomerulus, and a slight dilation of postglomerular vessels. Glomerular blood flow (GBF) was increased by NECA, and decreased by CHA and 2-CLA. The effects of CHA in reducing GBF were greater than those of 2-CLA. From these experiments it is concluded that vascular A1 and A2 adenosine receptors are present in the kidney and that activation of A1 receptors is associated with preglomerular vasoconstriction only, whereas activation of A2 receptors mediates pre- and postglomerular vasodilation with a lack of vasodilatory response of the distal afferent arteriole. Furthermore, these data indicate that nonselective occupation of both receptor subclasses is associated with marked vasoconstriction of the afferent arteriole and little vasodilation of the efferent arteriole.

摘要

本实验的目的是确定腺苷激动剂N-乙基-羧酰胺腺苷(NECA)、N6-环己基腺苷(CHA)和2-氯腺苷(2-CLA)对肾血管的影响。通过体内电视显微镜测量Inactin麻醉大鼠分侧肾积水肾脏中肾小球前和肾小球后血管的直径。所有代谢稳定的腺苷激动剂均局部应用于肾组织浴槽中。NECA是一种选择性A2腺苷受体激动剂,除了对肾小球附近的入球小动脉有轻微的收缩作用外,可诱导剂量依赖性的显著的肾小球前血管舒张和轻微的肾小球后血管舒张。应用CHA(一种选择性A1腺苷受体激动剂)导致所有肾小球前血管收缩,其收缩程度在入球小动脉最远端部分最大。2-CLA是一种非选择性激动剂,使所有肾小球前血管直径略有减小,使肾小球附近部位的入球小动脉显著收缩,并使肾小球后血管略有舒张。NECA使肾小球血流量(GBF)增加,CHA和2-CLA使其减少。CHA降低GBF的作用大于2-CLA。从这些实验可以得出结论,肾脏中存在血管A1和A2腺苷受体,A1受体的激活仅与肾小球前血管收缩有关,而A2受体的激活介导肾小球前和肾小球后血管舒张,且远端入球小动脉缺乏血管舒张反应。此外,这些数据表明,两种受体亚型的非选择性占据与入球小动脉的显著血管收缩和出球小动脉的轻微血管舒张有关。

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