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合成心房利钠因子的血管舒张特性

Vasodilator profile of synthetic atrial natriuretic factor.

作者信息

Winquist R J, Faison E P, Nutt R F

出版信息

Eur J Pharmacol. 1984 Jun 15;102(1):169-73. doi: 10.1016/0014-2999(84)90353-4.

Abstract

The vasodilator profile of synthetic atrial natriuretic factor (ANF) was characterized using isolated vascular preparations. Nanomolar concentrations of ANF relaxed rabbit aortic rings contracted by serotonin, histamine, methoxamine or angiotensin II. The synthetic peptide was most effective (IC50 = 1.3 X 10(-10) M) in relaxing the tonic, intrinsic contractions of the rabbit facial vein. ANF was poorly active against K+-contracted aortic rings or the phasic contractions of the rat portal vein. A similar vasodilator profile was obtained for sodium nitroprusside but not papaverine, hydralazine, adenosine or nifedipine. This first demonstration of the vascular activity of synthetic ANF depicts this substance as a nonselective vasodilator of agonist-induced contractions. The observed similarities in the vasodilator activity of ANF and sodium nitroprusside suggest a common mechanism of action.

摘要

使用离体血管制备物对合成心房利钠因子(ANF)的血管舒张特性进行了表征。纳摩尔浓度的ANF可使由5-羟色胺、组胺、甲氧明或血管紧张素II引起收缩的兔主动脉环舒张。合成肽在舒张兔面静脉的紧张性、自发性收缩方面最为有效(IC50 = 1.3×10⁻¹⁰ M)。ANF对钾离子引起收缩的主动脉环或大鼠门静脉的相性收缩作用较弱。硝普钠也呈现出类似的血管舒张特性,但罂粟碱、肼屈嗪、腺苷或硝苯地平则不然。合成ANF血管活性的首次证明表明该物质是激动剂诱导收缩的非选择性血管舒张剂。观察到的ANF和硝普钠血管舒张活性的相似性提示了共同的作用机制。

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