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红霉素和胃动素可刺激袋貂的奥迪括约肌运动,并抑制经括约肌的胆汁流动。

Erythromycin and motilin stimulate sphincter of Oddi motility and inhibit trans-sphincteric flow in the Australian possum.

作者信息

Saccone G T, Liu Y F, Thune A, Harvey J R, Baker R A, Toouli J

机构信息

Department of Surgery, Flinders Medical Centre, Bedford Park, South Australia.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1992 Dec;346(6):701-6. doi: 10.1007/BF00168745.

Abstract

The actions of erythromycin lactobionate and porcine motilin on trans-sphincteric flow and simultaneous sphincter of Oddi motility were studied in 15 anaesthetized Australian Brush-tailed possums (Trichosurus vulpecula). Erythromycin (25-200 micrograms/kg) and motilin (25-200 ng/kg) were administered as graded doses by close intraarterial injection. Trans-sphincteric flow was measured as inflow and outflow. Both motilin and erythromycin decreased trans-sphincteric inflow (both P < 0.0001) and outflow (P < 0.0001 and P = 0.0017 respectively) in a dose-dependent manner. The highest dose of each agent abolished trans-sphincteric flow. These agents increased sphincter of Oddi phasic contraction frequency and basal pressure up to 2 and 3 fold respectively (P < 0.05). The amplitude of the sphincter of Oddi phasic contractions were not influenced in any consistent fashion by either agent. The durations of the responses (trans-sphincteric inflow) elicited by erythromycin and motilin were dose dependent (P = 0.0225 and P = 0.0001 respectively). The actions of erythromycin (200 micrograms/kg) or motilin (100 ng/kg) on trans-sphincteric flow and sphincter of Oddi motility were not influenced by neural blockade with tetrodotoxin. These findings support the hypothesis that erythromycin acts as a motilin agonist and both substances increase the resistance to flow through the sphincter of Oddi by raising the basal pressure and frequency of contractions.

摘要

在15只麻醉的澳大利亚帚尾袋貂(帚尾袋貂)中研究了乳糖酸红霉素和猪胃动素对跨括约肌流量以及同时存在的Oddi括约肌运动的作用。通过动脉内近距离注射以分级剂量给予红霉素(25 - 200微克/千克)和胃动素(25 - 200纳克/千克)。跨括约肌流量通过流入量和流出量来测量。胃动素和红霉素均以剂量依赖性方式降低跨括约肌流入量(均P < 0.0001)和流出量(分别为P < 0.0001和P = 0.0017)。每种药物的最高剂量消除了跨括约肌流量。这些药物分别使Oddi括约肌的相性收缩频率和基础压力增加高达2倍和3倍(P < 0.05)。两种药物均未以任何一致的方式影响Oddi括约肌相性收缩的幅度。红霉素和胃动素引起的反应持续时间(跨括约肌流入量)呈剂量依赖性(分别为P = 0.0225和P = 0.0001)。红霉素(200微克/千克)或胃动素(100纳克/千克)对跨括约肌流量和Oddi括约肌运动的作用不受河豚毒素神经阻滞的影响。这些发现支持了以下假设,即红霉素作为胃动素激动剂起作用,并且两种物质通过提高基础压力和收缩频率来增加通过Oddi括约肌的流动阻力。

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