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阿片类药物在调节乙酰胆碱释放的作用位点之外的另一个作用位点调节肠道蠕动。

Opioids modulate intestinal peristalsis at a site of action additional to that modulating acetylcholine release.

作者信息

Kromer W, Schmidt H

出版信息

J Pharmacol Exp Ther. 1982 Oct;223(1):271-4.

PMID:7120123
Abstract

The nature of the interaction between cholinergic and opioid mechanisms controlling peristalsis in the intact segment of the guinea-pig ileum was examined. The induction of rhythmic peristaltic activity by acetylcholine was dose dependently inhibited and facilitated by preapplication of, respectively, normorphine and naloxone. The action of intestinal opioids occurs, at least partially, at a site of action differing from that modulating the release of acetylcholine from the myenteric plexus. Interruption of the peristaltic reflex by hexamethonium, atropine, tetrodotoxin or desensitization of the segments to serotonin also strongly impaired or abolished the initiation of circular muscle contractions produced by naloxone. Therefore, no indication could be found for a direct action of naloxone upon the circular muscle. Rather, intestinal opioids appear to be involved in regulating the activity of the reflex arc.

摘要

研究了豚鼠回肠完整段中控制蠕动的胆碱能和阿片类机制之间相互作用的性质。乙酰胆碱诱导的节律性蠕动活动分别被去甲吗啡和纳洛酮预先应用而剂量依赖性地抑制和促进。肠道阿片类药物的作用至少部分发生在与调节乙酰胆碱从肌间神经丛释放的作用部位不同的作用部位。六甲铵、阿托品、河豚毒素对蠕动反射的阻断或节段对5-羟色胺的脱敏也强烈损害或消除了纳洛酮引起的环行肌收缩的起始。因此,未发现纳洛酮对环行肌有直接作用的迹象。相反,肠道阿片类药物似乎参与调节反射弧的活动。

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