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腺苷受体激动剂对离体灌注大鼠肾脏的影响。

Effects of adenosine receptor agonists in the isolated, perfused rat kidney.

作者信息

Murray R D, Churchill P C

出版信息

Am J Physiol. 1984 Sep;247(3 Pt 2):H343-8. doi: 10.1152/ajpheart.1984.247.3.H343.

Abstract

Two subclasses of adenosine receptors, A1 and A2, have been described. The purpose of these experiments was to determine and compare the renal effects of several adenosine receptor agonists: adenosine (Ado), 2-chloroadenosine (2CA, nonselective), N6-cyclohexyladenosine (CHA, A1 selective), and N6-ethylcarboxamide adenosine (NECA, A2 selective). Rat kidneys were perfused at constant pressure (105 +/- 5 mmHg) using a Krebs-Henseleit buffer containing 3.5 g/100 ml Ficoll and 1.0 g/100 ml bovine serum albumin. Three clearance periods were obtained in each kidney, i.e., control, experimental [drug at 1 microM or vehicle (NaCl)], and recovery. Perfusate flow was increased by Ado, 2CA, and NECA but not affected by CHA. Glomerular filtration was increased by NECA, decreased by CHA, and not affected by Ado and 2CA. Afferent arteriolar resistance was decreased by NECA, increased by CHA, and unaffected by Ado and 2CA. Efferent arteriolar resistance was decreased by all agonists. CHA tended to decrease renin secretion whereas NECA significantly increased it. The results suggest that the renal vasculature possesses both A1 and A2 adenosine receptors and that activation of A2 receptors mediates arteriolar dilation and stimulation of renin secretion whereas activation of A1 receptors mediates arteriolar constriction and possibly inhibition of renin secretion.

摘要

已描述了腺苷受体的两个亚类,即A1和A2。这些实验的目的是确定并比较几种腺苷受体激动剂对肾脏的影响:腺苷(Ado)、2 - 氯腺苷(2CA,非选择性)、N6 - 环己基腺苷(CHA,A1选择性)和N6 - 乙基羧酰胺腺苷(NECA,A2选择性)。使用含有3.5 g/100 ml 聚蔗糖和1.0 g/100 ml 牛血清白蛋白的 Krebs - Henseleit 缓冲液,以恒定压力(105±5 mmHg)灌注大鼠肾脏。每个肾脏获得三个清除期,即对照期、实验期[1 μM药物或溶剂(NaCl)]和恢复期。Ado、2CA和NECA可增加灌注液流量,但CHA对其无影响。NECA可增加肾小球滤过率,CHA使其降低,而Ado和2CA对其无影响。NECA可降低入球小动脉阻力,CHA使其增加,Ado和2CA对其无影响。所有激动剂均可降低出球小动脉阻力。CHA倾向于降低肾素分泌,而NECA则显著增加肾素分泌。结果表明,肾血管系统同时具有A1和A2腺苷受体,A2受体的激活介导小动脉扩张和肾素分泌的刺激,而A1受体的激活介导小动脉收缩并可能抑制肾素分泌。

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