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E 前列腺素对犬胃电位差的影响。

Effects of E prostaglandins on canine gastric potential difference.

作者信息

Dajani E Z, Callison D A, Bertermann R E

出版信息

Am J Dig Dis. 1978 May;23(5):436-42. doi: 10.1007/BF01072927.

Abstract

Measurement of the gastric transmucosal potential difference (PD) was used to study the effect of gastric antisecretory prostaglandins on the integrity of the gastric mucosa of the Heidenhain pouch dog. Intragastric administration of SC-29333 [(+/-)-15-deoxy-16-alpha,beta-hydroxy-16-methyl PGE1 methyl ester] slightly but significantly increased the transmucosal PD when compared to vehicle control. In addition, SC-29333 administered either intravenously or intragastrically, significantly inhibited the PD fall induced by aspirin, a well-established barrier breaker. In contrast, the intragastric administration of 16,16-dimethyl PGE2 methyl ester (Me-PGE2) significantly lowered the transmucosal PD and failed to modify the actions of aspirin on the integrity of the gastric mucosa. However, the intravenous administration of either prostaglandin did not affect the basal transmucosal PD values. These studies suggest that SC-29333 may strengthen the integrity of the gastric mucosal barrier against aspirin, and this could have important therapeutic potential.

摘要

采用测量胃黏膜跨膜电位差(PD)的方法,研究胃抗分泌前列腺素对海登海因小胃犬胃黏膜完整性的影响。与溶剂对照组相比,胃内给予SC - 29333 [(±)-15 - 脱氧-16 - α,β-二羟基-16 - 甲基前列腺素E1甲酯]可使跨膜PD轻微但显著升高。此外,静脉内或胃内给予SC - 29333均可显著抑制由阿司匹林(一种公认的屏障破坏剂)诱导的PD下降。相反,胃内给予16,16 - 二甲基前列腺素E2甲酯(Me - PGE2)可显著降低跨膜PD,并且不能改变阿司匹林对胃黏膜完整性的作用。然而,静脉内给予这两种前列腺素均不影响基础跨膜PD值。这些研究表明,SC - 29333可能增强胃黏膜屏障对阿司匹林的抵抗力,这可能具有重要的治疗潜力。

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