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地西泮对氨基甲酸乙酯麻醉下大鼠连续灌流胃胃酸分泌的刺激作用。

Stimulatory effect of diazepam on gastric acid secretion in the continuously perfused stomach in rats under urethane anesthesia.

作者信息

Lin W C

机构信息

Department of Pharmacology, China Medical College, Taichung, Taiwan, R.O.C.

出版信息

Res Commun Mol Pathol Pharmacol. 1997 Feb;95(2):157-68.

PMID:9090752
Abstract

The effects of diazepam, a typical benzodiazepine receptor agonist, on gastric acid secretion were studied in both conscious pylorus-ligated rats and the perfused stomach of rats under urethane anesthesia. Diazepam did not affect acid secretion in conscious pylorus-ligated rats. Under urethane anesthesia, diazepam showed a definite stimulation on gastric acid secretion. However this stimulatory action was caused neither by 4'-chlordiazepam, which is a peripheral benzodiazepine receptor agonist, nor beta-carbline-3-carboxylic acid methyl ester, which is an inverse benzodiazepine receptor agonist. Pretreatment with atropine, hexamethonium or bilateral truncal vagotomy inhibited the diazepam-induced acid secretion. Pretreatment with flumazenil, which is a benzodiazepine receptor antagonist, reduced the acid secretion induced by diazepam, but pretreatment with 1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxam ide, which is a peripheral benzodiazepine receptor antagonist, did not reduce the acid secretion induced by diazepam. 3-Mercaptopropionic acid, which is an inhibitor of GABA biosynthesis, picrotoxin and pentylenetetrazol inhibited diazepam-stimulated acid secretion. Gastric acid secretion stimulated by baclofen was not affected by flumazenil, 3-mercaptopropionic acid or picrotoxin. These results suggest that acid secretion is centrally stimulated by diazepam in rats under anesthesia, and the stimulatory action is closely associated with benzodiazepine-GABA complex receptors.

摘要

在清醒的幽门结扎大鼠和氨基甲酸乙酯麻醉下的大鼠灌流胃中,研究了典型的苯二氮䓬受体激动剂地西泮对胃酸分泌的影响。地西泮对清醒的幽门结扎大鼠的胃酸分泌没有影响。在氨基甲酸乙酯麻醉下,地西泮对胃酸分泌有明确的刺激作用。然而,这种刺激作用既不是由外周苯二氮䓬受体激动剂4'-氯地西泮引起的,也不是由反向苯二氮䓬受体激动剂β-咔啉-3-羧酸甲酯引起的。用阿托品、六甲铵或双侧迷走神经切断术预处理可抑制地西泮诱导的胃酸分泌。用苯二氮䓬受体拮抗剂氟马西尼预处理可减少地西泮诱导的胃酸分泌,但用外周苯二氮䓬受体拮抗剂1-(2-氯苯基)-N-甲基-N-(1-甲基丙基)-3-异喹啉甲酰胺预处理并不能减少地西泮诱导的胃酸分泌。γ-氨基丁酸生物合成抑制剂3-巯基丙酸、苦味毒和戊四氮可抑制地西泮刺激的胃酸分泌。巴氯芬刺激的胃酸分泌不受氟马西尼、3-巯基丙酸或苦味毒的影响。这些结果表明,在麻醉大鼠中,地西泮可通过中枢刺激胃酸分泌,且这种刺激作用与苯二氮䓬-GABA复合受体密切相关。

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