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犬一氧化氮合酶抑制剂所致高血压的神经机制

Neural mechanism of hypertension by nitric oxide synthase inhibitor in dogs.

作者信息

Toda N, Kitamura Y, Okamura T

机构信息

Department of Pharmacology, Shiga University of Medical Sciences, Ohtsu, Japan.

出版信息

Hypertension. 1993 Jan;21(1):3-8. doi: 10.1161/01.hyp.21.1.3.

Abstract

This study aimed to determine the mechanism of hypertension associated with nitric oxide synthase inhibition. Intravenous injections of NG-nitro-L-arginine, a nitric oxide synthase inhibitor, produced a sustained increase in systemic blood pressure and a decrease in heart rate in anesthetized dogs, whereas NG-nitro-D-arginine had no effect. L-Arginine reversed the pressor response. NG-Nitro-L-arginine-induced hypertension was markedly attenuated or abolished by treatment with hexamethonium; this inhibition was still observed when the blood pressure fall caused by the ganglionic blocking agent was compensated by continuous infusion of angiotensin II. In dogs treated with phentolamine in a dose sufficient to lower blood pressure to the level similar to that elicited by hexamethonium and to suppress the pressor response to norepinephrine, the hypertensive effect of NG-nitro-L-arginine was not attenuated. We conclude that hypertension caused by the nitric oxide synthase inhibitor is associated with an elimination of nitroxidergic neural function rather than an impairment of the basal release of nitric oxide from the endothelium.

摘要

本研究旨在确定与一氧化氮合酶抑制相关的高血压机制。静脉注射一氧化氮合酶抑制剂NG-硝基-L-精氨酸可使麻醉犬的全身血压持续升高并使心率降低,而NG-硝基-D-精氨酸则无此作用。L-精氨酸可逆转升压反应。六甲铵治疗可使NG-硝基-L-精氨酸诱导的高血压明显减轻或消除;当通过持续输注血管紧张素II补偿神经节阻断剂引起的血压下降时,仍可观察到这种抑制作用。在用足以将血压降至与六甲铵引起的血压水平相似并抑制对去甲肾上腺素的升压反应的剂量的酚妥拉明治疗的犬中,NG-硝基-L-精氨酸的高血压作用并未减弱。我们得出结论,一氧化氮合酶抑制剂引起的高血压与硝氧能神经功能的消除有关,而不是与内皮一氧化氮基础释放受损有关。

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