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Clinical experience with impromidine, a highly specific H2-receptor agonist.

作者信息

Bangerter U, Schlup M, Liechti M, Häcki W H, Halter F

出版信息

Digestion. 1981;22(4):196-202. doi: 10.1159/000198645.

DOI:10.1159/000198645
PMID:6458522
Abstract

The gastric secretory response to impromidine (SKF 92676), a potent selective histamine H2 agonist, has been studied in 40 patients with peptic ulcer disease or ulcer-like dyspepsia. Peak acid output following the intravenous infusion of impromidine, 10 micrograms kg-1h-1, or pentagastrin, 6 micrograms kg-1h-1, was not significantly different. This was also the case when the two drugs were administered subcutaneously at the same dose. Impromidine was well tolerated with only minor effects on the cardiovascular system both in 10 younger patients and in 20 subjects over the age of 55 years with mild to moderate cardiovascular disease. Impromidine can be considered an important tool for further investigation of the role of histamine at the H2-receptor site in man.

摘要

相似文献

1
Clinical experience with impromidine, a highly specific H2-receptor agonist.
Digestion. 1981;22(4):196-202. doi: 10.1159/000198645.
2
Gastric secretory studies in humans with impromidine (SK&F 92676)--a specific histamine H2 receptor agonist.使用英普咪定(SK&F 92676)——一种特异性组胺H2受体激动剂,对人体进行胃分泌研究。
Gastroenterology. 1980 Mar;78(3):505-11.
3
Gastric mucosal blood flow and acid secretory changes in man with impromidine: a new specific histamine-H2-receptor agonist.用英普咪定(一种新型特异性组胺-H2受体激动剂)对人体胃黏膜血流及胃酸分泌变化的研究
Gut. 1981 Jul;22(7):529-33. doi: 10.1136/gut.22.7.529.
4
Dose-response curve analysis of gastric secretory responses in the dog and man to impromidine: a new histamine-H2-receptor agonist.犬和人对英普咪定(一种新型组胺H2受体激动剂)的胃分泌反应的剂量-反应曲线分析
J Pharmacol Exp Ther. 1983 Apr;225(1):186-90.
5
Histamine H2 receptors and intrinsic factor secretion.组胺H2受体与内因子分泌
Scand J Gastroenterol. 1980;15(3):377-84. doi: 10.3109/00365528009181487.
6
Cardiovascular studies with impromidine (SK&F 92676), a new very potent and specific histamine H2-receptor agonist.使用新型强效特异性组胺H2受体激动剂英普咪定(SK&F 92676)进行的心血管研究。
J Pharm Pharmacol. 1979 Sep;31(9):577-82. doi: 10.1111/j.2042-7158.1979.tb13595.x.
7
Comparison of the agonist activity of impromidine (SK & F 92676) in anaesthetized rabbits and on the rabbit isolated fundic mucosa.在麻醉兔体内及兔离体胃底黏膜上,比较英普咪定(SK & F 92676)的激动剂活性。
Br J Pharmacol. 1981 Aug;73(4):917-9. doi: 10.1111/j.1476-5381.1981.tb08746.x.
8
Impromidine (SK & F 92676) acts as a partial agonist on the isolated whole stomach of the rat.英普咪定(SK&F 92676)对大鼠离体全胃起部分激动剂的作用。
Br J Pharmacol. 1980 May;69(1):6-7. doi: 10.1111/j.1476-5381.1980.tb10874.x.
9
Hypersensitivity of gastric parietal cells to selective H2-receptor stimulation in duodenal ulcer.十二指肠溃疡中胃壁细胞对选择性H2受体刺激的超敏反应。
Hepatogastroenterology. 1984 Apr;31(2):88-90.
10
Impromidine, a potent dilator of cat pial arterioles.
Eur J Pharmacol. 1981 Jul 17;73(2-3):225-7. doi: 10.1016/0014-2999(81)90096-0.

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