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作为潜在降压药的甲氧明氨基四氢萘类似物。

Aminotetralin analogs of methoxamine as potential hypertensive agents.

作者信息

Sharabi F M, Long J P, Rusterholz D B, Barfknecht C F

出版信息

Res Commun Chem Pathol Pharmacol. 1978 Jan;19(1):37-55.

PMID:625593
Abstract

Cardiovascular effects of methoxamine and some aminotetralin derivatives (5,8-ADT, DR-31 and DR-17) were studied after systemic intravenous or intraarterial injection into different perfused vascular beds in anesthetized dogs. Intravenous administration of the compounds produced dose-related prolonged increases in blood pressure, which were antagonized by phentolamine. After intro-arterial injection into the perfused hindlimb, mesenteric artery or the saphenous vein, all compounds produced dose-dependent increases in perfusion pressure indicative of vasoconstriction. Phentolamine antagonized these effects. It was demonstrated that desipramine significantly reduced the vasoconstricting actions of intra-arterially injected tyramine in the hindlimb, but did not alter the responses induced by methoxamine and the aminotetralin derivatives. The data indicate that these compounds elicit peripheral vasoconstriction in the dog, through a direct action on the alpha adrenergic receptors.

摘要

在麻醉犬的不同灌注血管床中,经全身静脉或动脉注射后,研究了甲氧明和一些氨基四氢萘衍生物(5,8-ADT、DR-31和DR-17)的心血管效应。静脉注射这些化合物会使血压出现剂量相关的持续升高,酚妥拉明可拮抗这种作用。将这些化合物动脉内注射到灌注的后肢、肠系膜动脉或大隐静脉后,所有化合物都会使灌注压出现剂量依赖性升高,表明有血管收缩作用。酚妥拉明可拮抗这些效应。已证明地昔帕明可显著降低动脉内注射酪胺在后肢引起的血管收缩作用,但不改变甲氧明和氨基四氢萘衍生物所诱导的反应。数据表明,这些化合物通过直接作用于α肾上腺素能受体在犬体内引起外周血管收缩。

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