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腔面Nα-甲基组胺通过释放胃泌素刺激十二指肠溃疡患者的胃酸分泌。

Luminal Nalpha-methyl histamine stimulates gastric acid secretion in duodenal ulcer patients via releasing gastrin.

作者信息

Konturek P C, Konturek S J, Sito E, Kwiecien N, Obtulowicz W, Bielanski W, Hahn E G

机构信息

Department of Medicine, Erlangen-Nuremberg University, Erlangen, Germany.

出版信息

Eur J Pharmacol. 2001 Jan 26;412(2):181-5. doi: 10.1016/s0014-2999(01)00720-8.

Abstract

Nalpha-methyl histamine is an unusual histamine metabolite which is produced in the stomach infected by Helicobacter pylori and which was shown in animals to stimulate gastric acid secretion and to release gastrin in vitro isolated G-cells, but no information is available regarding its influence on gastric secretion and gastrin release in duodenal ulcer patients before and after H. pylori eradication. In this study, we compared the effects of intragastric administration of single or graded doses of Nalpha-methyl histamine on gastric acid secretion and plasma gastrin levels in 16 male duodenal ulcer patients (aging from 35 to 48 years and weighing 65-82 kg) before and after the eradication of H. pylori. Furthermore, the gastric luminal histamine and gastrin contents were determined before and after H. pylori eradication. In H. pylori-infected duodenal ulcer patients, the intragastric application of Nalpha-methyl histamine failed to affect gastric acid secretion or plasma gastrin levels. Following eradication of H. pylori, gastric luminal histamine and gastrin, and both basal gastric acid secretion and plasma gastrin levels, were significantly reduced. Nalpha-methyl histamine given intragastrically in graded doses to such H. pylori-eradicated duodenal ulcer patients was found to increase dose-dependently gastric acid output reaching at a dose of 5 mg, about 80% of histamine maximum induced by i.v. infusion of 25 microg/kg h of histamine dihydrochloride. We conclude that Nalpha-methyl histamine is a potent luminally active stimulant of gastrin release and gastric acid secretion in H. pylori-eradicated patients when luminal histamine is low but is not effective in H. pylori infected patients when luminal histamine is enhanced, possibly due to desensitization of gastrin (G-cells) and acid-producing (parietal) cells by Nalpha-methyl histamine produced excessively in H. pylori-infected stomach.

摘要

Nα-甲基组胺是一种特殊的组胺代谢产物,由感染幽门螺杆菌的胃产生,在动物实验中显示可刺激胃酸分泌,并在体外分离的G细胞中释放胃泌素,但关于其对十二指肠溃疡患者在根除幽门螺杆菌前后胃酸分泌和胃泌素释放的影响尚无相关信息。在本研究中,我们比较了16名男性十二指肠溃疡患者(年龄35至48岁,体重65 - 82千克)在根除幽门螺杆菌前后,胃内给予单次或分级剂量的Nα-甲基组胺对胃酸分泌和血浆胃泌素水平的影响。此外,还测定了根除幽门螺杆菌前后胃腔内组胺和胃泌素的含量。在感染幽门螺杆菌的十二指肠溃疡患者中,胃内应用Nα-甲基组胺未能影响胃酸分泌或血浆胃泌素水平。根除幽门螺杆菌后,胃腔内组胺和胃泌素以及基础胃酸分泌和血浆胃泌素水平均显著降低。给根除幽门螺杆菌的十二指肠溃疡患者胃内分级给予Nα-甲基组胺,发现其可剂量依赖性地增加胃酸分泌,在剂量为5毫克时,达到静脉输注25微克/千克·小时盐酸组胺诱导的组胺最大分泌量约80%。我们得出结论,在根除幽门螺杆菌的患者中,当胃腔内组胺水平较低时,Nα-甲基组胺是一种有效的胃腔内促胃泌素释放和胃酸分泌的刺激物,但在幽门螺杆菌感染患者中,当胃腔内组胺水平升高时则无效,这可能是由于幽门螺杆菌感染的胃中过度产生的Nα-甲基组胺使胃泌素(G细胞)和产酸(壁细胞)细胞脱敏所致。

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