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Histidine decarboxylase inhibition by O-methyl-3(+)catechin and gastric acid secretion in the cat.

作者信息

Albinus M, Frisch G, Hennings G

出版信息

Agents Actions. 1983 Apr;13(2-3):249-51. doi: 10.1007/BF01967344.

DOI:10.1007/BF01967344
PMID:6869127
Abstract

In the conscious cat the histidine decarboxylase inhibitor O-methyl-3(+)catechin (Zy 15029) promoted a dose-dependent atropine-sensitive increase in basal acid output. Gastric acid secretion stimulated by food or insulin at different time intervals after pretreatment with Zy 15029 was dose and time dependently diminished up to 70% whereas acid output following pentagastrin stimulation was not reduced by doses effective against the former two stimuli. Only a high dose, which due to side effects has to be claimed as not tolerable in the cat, reduced acid output by about 40%, when application of Zy 15029 and stimulation were 90 min apart. It is suggested that in the cat gastric acid response following the three different stimuli was at least in part but to a variable extent mediated by endogenous histamine. Dose-dependent side effects of Zy 15029 might have been due to histidine decarboxylase inhibition in brain and changes in histaminergic neurotransmission.

摘要

相似文献

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引用本文的文献

1
Histidine decarboxylase inhibition: a novel approach towards the development of an effective and safe gastric anti-ulcer drug.组氨酸脱羧酶抑制作用:一种开发有效且安全的抗胃溃疡药物的新方法。
Agents Actions. 1984 Dec;15(5-6):494-9. doi: 10.1007/BF01966762.

本文引用的文献

1
Gastric anti-ulcer activity of (+)-cyanidanol-3, a histidine decarboxylase inhibitor.
Eur J Pharmacol. 1981 Jan 5;69(1):25-32. doi: 10.1016/0014-2999(81)90598-7.
2
Pharmacologic control of temperature regulation.体温调节的药物控制
Annu Rev Pharmacol Toxicol. 1977;17:341-53. doi: 10.1146/annurev.pa.17.040177.002013.
3
Histaminergic mechanisms in brain.大脑中的组胺能机制。
Annu Rev Pharmacol Toxicol. 1977;17:325-39. doi: 10.1146/annurev.pa.17.040177.001545.