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[麻醉性镇痛药、氟哌利多、地西泮和氟硝西泮对小动脉平滑肌的影响(作者译)]

[Influence of narcotic analgesics, droperidol, diazepam, and flunitrazepam on the smooth muscles of small arteries (author's transl)].

作者信息

Pasch T, Bugsch L A

出版信息

Anaesthesist. 1979 Jun;28(6):283-9.

PMID:37771
Abstract

In isolated segments of the rat tail artery, the influence of narcotic analgesics, their antagonists, droperidol, diazepam, and flunitrazepam on the vascular smooth muscle was investigated. The wall of this vessel consists of about 75 per cent smooth muscle fibres. For all agents studied, pressure-diameter relations were determined before and after a virtually maximum constriction which was induced with noradrenaline. The results were compared with those obtained under control conditions, i.e. prior to the addition of the drugs to the bath solution. Tested in pure Tyrode's solution, none of the agents produced a noticeable constriction or relaxation. Among the analgesics and their antagonists, morphine was the most potent in inhibiting the noradrenaline-induced constriction of the vessel (mean increase in diameter 15%). Pentazocine and levallorphan were less effective (mean increase 8%), and the administration of pethidine and naloxone was followed by even less relaxation, resulting in mean diameter increases of 4%. Piritramide and fentanyl did not show any effect. Depending on the pressure level, droperidol caused the diameter to increase 2 to 10%. Flunitrazepam brought about a marked relaxation (mean increase in diameter 15%), diazepam, however, did not influence the vessel segments. The results obtained show that the haemodynamic effects of the drugs used in this study, in particular those on the peripheral resistance, may, at least partially, be due to their direct influences on the vascular smooth muscle. The real pharmacologic mechanisms by which these effects are initiated, in most cases still remain to be investigated.

摘要

在大鼠尾动脉的离体节段中,研究了麻醉性镇痛药、其拮抗剂、氟哌利多、地西泮和氟硝西泮对血管平滑肌的影响。该血管壁约由75%的平滑肌纤维组成。对于所有研究的药物,在使用去甲肾上腺素诱导几乎最大程度收缩前后测定压力-直径关系。将结果与在对照条件下(即在向浴液中添加药物之前)获得的结果进行比较。在纯台氏液中进行测试时,这些药物均未产生明显的收缩或舒张作用。在镇痛药及其拮抗剂中,吗啡抑制去甲肾上腺素诱导的血管收缩作用最强(直径平均增加15%)。喷他佐辛和烯丙左吗喃的效果较差(平均增加8%),而给予哌替啶和纳洛酮后舒张作用更小,直径平均增加4%。匹利卡明和芬太尼未显示任何作用。根据压力水平,氟哌利多使直径增加2%至10%。氟硝西泮引起明显的舒张(直径平均增加15%),然而,地西泮对血管节段没有影响。所获得的结果表明,本研究中使用的药物的血流动力学效应,特别是对周围阻力的效应,至少部分可能是由于它们对血管平滑肌的直接影响。在大多数情况下,引发这些效应的真正药理机制仍有待研究。

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