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双氢麦角毒碱在大鼠体内的α-肾上腺素能激动剂和拮抗剂活性。

Alpha-adrenergic agonist and antagonist activity of dihydroergotoxine in rats.

作者信息

Roquebert J, Demichel P

出版信息

J Pharm Pharmacol. 1985 Jun;37(6):415-20. doi: 10.1111/j.2042-7158.1985.tb03026.x.

Abstract

The alpha-adrenergic activity of dihydroergotoxine had been studied in both pithed and urethane or pentobarbitone anaesthetized rats. In anaesthetized rats, blood pressure effects varied with the anaesthetic agent: hypotension with urethane, hypertension with pentobarbitone. This latter pressor response was a peripheral effect. In pithed rats, the vasopressor response to dihydroergotoxine was reduced competitively by yohimbine, and non-competitively by nifedipine, but not by prazosin or methysergide, showing that the vasoconstriction is mediated by alpha 2-adrenoceptors. Dihydroergotoxine decreases the tachycardia elicited by stimulation of the cardioaccelerator nerves, this effect being antagonized by yohimbine. It also reduced the pressor response to (-)-phenylephrine. These results indicated that, on the peripheral vascular system of the rat, dihydroergotoxine acts as an alpha 1-adrenoceptor blocker and an alpha 2-adrenoceptor agonist.

摘要

已在脊髓横断及经乌拉坦或戊巴比妥麻醉的大鼠中研究了双氢麦角毒碱的α-肾上腺素能活性。在麻醉大鼠中,血压效应因麻醉剂而异:乌拉坦导致低血压,戊巴比妥导致高血压。后一种升压反应是外周效应。在脊髓横断大鼠中,育亨宾竞争性地降低了双氢麦角毒碱的血管升压反应,硝苯地平非竞争性地降低了该反应,但哌唑嗪或甲基麦角新碱则无此作用,表明血管收缩是由α2-肾上腺素能受体介导的。双氢麦角毒碱可降低刺激心脏加速神经引起的心动过速,育亨宾可拮抗此效应。它还降低了对(-)-去氧肾上腺素的升压反应。这些结果表明,在大鼠外周血管系统上,双氢麦角毒碱起α1-肾上腺素能受体阻滞剂和α2-肾上腺素能受体激动剂的作用。

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