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Histamine and acute haemorrhagic lesions in rat gastric mucosa: prevention of stress ulcer formation by (+)-catechin, an inhibitor of specific histidine decarboxylase in vitro.

作者信息

Reimann H J, Lorenz W, Fischer M, Frölich R, Meyer H J, Schmal A

出版信息

Agents Actions. 1977 Mar;7(1):69-73. doi: 10.1007/BF01964883.

DOI:10.1007/BF01964883
PMID:871094
Abstract

Acute haemorrhagic lesions in the oesophagus, stomach and duodenum ('stress ulcers') occur relatively often under clinical conditions and are always dangerous to the patient (lethality rate about 70%). Since conservative and surgical treatment are without significant success up to now, prevention by adaptation to stressors or by administration of drugs seems mandatory. An improved technique for producing acute gastric lesions in rats by immobilization and a new method for assessing this disease in the animals is presented in this communication. High precision is obtained within a single experimental series especially from day to day. Since histamine was suggested to be involved in the pathogenesis of stress ulcer disease, (+)-catechin, a rather specific inhibitor of specific histidine decarboxylase from rat stomach, was tested in immobilized rats. It prevented the formation of acute gastric lesions by 80% in seven series of experiments lasting for half a year. Since the drug has low toxicity in man, it is recommended for clinical trials.

摘要

相似文献

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The gastric antisecretory activity of 3-methoxy-5,7,3'4'-tetrahydroxyflavan (ME)--a specific histidine decarboxylase inhibitor in rats.
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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。
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Gastric protection by meciadanol. A new synthetic flavonoid inhibiting histidine decarboxylase.美西达醇的胃保护作用。一种新型合成黄酮类化合物,可抑制组氨酸脱羧酶。
Dig Dis Sci. 1986 Aug;31(8):847-52. doi: 10.1007/BF01296054.
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