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[人胃酸抑制及硫前列素EMD 33290预防跨黏膜电位差下降]

[Human acid inhibition and prevention of a drop in the transmucosal potential difference by thioprostaglandin EMD 33290].

作者信息

Dammann H G, Müller P, Heun J, Simon B

出版信息

Schweiz Med Wochenschr. 1982 Jun 5;112(23):829-31.

PMID:7100879
Abstract

The effect of graded doses of EMD 33290 on basal acid secretion in healthy volunteers was tested over a time period of 6 hours. In addition, studies were conducted to determine if pretreatment with this thioprostaglandin could prevent the characteristic fall in human gastric potential difference associated with intragastric instillation of 1,000 mg aspirin or of 50 ml 4 mmol/l sodium taurocholate. Basal acid output was reduced by 65% and 75% after a 2 and 3 mg single dose of EMD 33290 respectively. 1 mg of this prostaglandin E2 analog showed no detectable antisecretory activity. EMD 33290 in a single dose of 50 micrograms and 250 micrograms effectively protected human gastric mucosa against the injurious effects of aspirin and sodium taurocholate. It is therefore concluded that EMD 33290 has two distinct properties in the human stomach, viz. antisecretory and protective, which are independent of each other.

摘要

在6小时的时间段内测试了不同剂量的EMD 33290对健康志愿者基础胃酸分泌的影响。此外,还进行了研究以确定用这种硫代前列腺素预处理是否可以预防与胃内滴注1000 mg阿司匹林或50 ml 4 mmol/l牛磺胆酸钠相关的人胃电位差的特征性下降。单次给予2 mg和3 mg EMD 33290后,基础胃酸分泌分别减少了65%和75%。1 mg这种前列腺素E2类似物未显示出可检测到的抗分泌活性。单次给予50微克和250微克的EMD 33290可有效保护人胃黏膜免受阿司匹林和牛磺胆酸钠的损伤作用。因此得出结论,EMD 33290在人胃中有两种不同的特性,即抗分泌和保护作用,且这两种作用相互独立。

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