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新型毒蕈碱拮抗剂药物哌仑西平对人体胰腺分泌的作用。

Action of pirenzepine, a new muscarinic antagonist drug, on human pancreatic secretion.

作者信息

Nishimura S, Laugier R, Sarles H

出版信息

Scand J Gastroenterol. 1985 Oct;20(8):990-4. doi: 10.3109/00365528509088860.

Abstract

The action of a new muscarinic antagonist drug on the pancreatic secretion has been studied in 12 healthy subjects. A stable pancreatic secretory plateau was obtained with submaximal hormonal stimulation (0.125 CU/kg/h secretin: 30 ng/kg/h caerulein). The highest dose of pirenzepine (40 mg) inhibited both volume and enzymatic concentration and output (-72.2% and -77.9% of plateau value for chymotrypsin and lipase output, respectively, 30 min after pirenzepine injection). The inhibition appeared immediately, lasted for more than 60 min, and was dose-related. The calcium dose-response curve paralleled those of lipase and chymotrypsin outputs. These results were comparable to those obtained with other anti-acetylcholine drugs and may be associated with the action of certain doses of ethanol on pancreatic secretion. In contrast, the lowest pirenzepine dose used (10 mg) induced a delayed stimulation of bicarbonate output, and bicarbonate concentration was not altered.

摘要

在12名健康受试者中研究了一种新型毒蕈碱拮抗剂药物对胰腺分泌的作用。通过次最大激素刺激(0.125 CU/kg/h促胰液素:30 ng/kg/h雨蛙素)获得了稳定的胰腺分泌平台。哌仑西平的最高剂量(40 mg)抑制了体积、酶浓度和输出(注射哌仑西平30分钟后,糜蛋白酶和脂肪酶输出分别为平台值的-72.2%和-77.9%)。抑制作用立即出现,持续超过60分钟,且与剂量相关。钙剂量反应曲线与脂肪酶和糜蛋白酶输出的曲线平行。这些结果与用其他抗乙酰胆碱药物获得的结果相当,并且可能与一定剂量乙醇对胰腺分泌的作用有关。相比之下,所用的最低哌仑西平剂量(10 mg)引起了碳酸氢盐输出的延迟刺激,且碳酸氢盐浓度未改变。

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