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腺苷类似物对兔肾皮质切片肾素释放的抑制作用。

Inhibition of renin release by analogues of adenosine in rabbit renal cortical slices.

作者信息

Barchowsky A, Data J L, Whorton A R

出版信息

Hypertension. 1987 Jun;9(6):619-23. doi: 10.1161/01.hyp.9.6.619.

Abstract

Renal cortical slices obtained from male New Zealand rabbits were used to investigate the role of adenosine in the regulation of renin release. Isoproterenol produced a significant (p less than 0.01), twofold to threefold increase in renin release, that was both dose-dependent and time-dependent. Addition of either the l-phenylisopropyl or the N6-ethylcarboxamido derivative of adenosine attenuated this stimulation at concentrations as low as 10(-9) M or 10(-8) M, respectively. Higher doses of d-phenylisopropyladenosine (10(-6) M) or adenosine (10(-5) M) were necessary to significantly reduce the beta-adrenergic response (p less than 0.01). Inhibition was absent in slices preincubated with 10(-5) M 8-phenyltheophylline, a concentration that had no effect on either basal or stimulated renin release. The site of inhibition appeared to be distal to beta-adrenergic and prostaglandin receptors since l-phenylisopropyladenosine (10(-8) M) blocked stimulation by selective beta-adrenergic receptor agonists, prenalterol (10(-6) M) or salbutamol (10(-5) M), and by prostaglandin E1. These data suggest that adenosine and its analogues inhibit renin release and that this inhibition may be mediated by a receptor-dependent action on a common point in the pathway leading to release.

摘要

从雄性新西兰兔获取的肾皮质切片被用于研究腺苷在肾素释放调节中的作用。异丙肾上腺素使肾素释放显著增加(p小于0.01),增加了两倍到三倍,且呈剂量依赖性和时间依赖性。分别添加低至10(-9)M或10(-8)M浓度的腺苷的l-苯异丙基或N6-乙基羧酰胺衍生物可减弱这种刺激。更高剂量的d-苯异丙基腺苷(10(-6)M)或腺苷(10(-5)M)才能显著降低β-肾上腺素能反应(p小于0.01)。用10(-5)M 8-苯茶碱预孵育的切片中没有抑制作用,该浓度对基础或刺激的肾素释放均无影响。抑制位点似乎在β-肾上腺素能和前列腺素受体的下游,因为l-苯异丙基腺苷(10(-8)M)可阻断选择性β-肾上腺素能受体激动剂普瑞特罗(10(-6)M)或沙丁胺醇(10(-5)M)以及前列腺素E1引起的刺激。这些数据表明腺苷及其类似物可抑制肾素释放,且这种抑制可能是通过对导致释放的途径中的一个共同点的受体依赖性作用介导的。

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