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16,16-二甲基前列腺素E2对犬胃酸分泌及胃黏膜氢离子通透性的局部作用

Topical effects of 16,16 dimethyl prostaglandin E2 on gastric acid secretion and mucosal permeability to hydrogen ions in dogs.

作者信息

Cheung L Y, Lowry S F, Perry J, Larson K

出版信息

Gut. 1978 Sep;19(9):775-8. doi: 10.1136/gut.19.9.775.

Abstract

The effects of luminal instillation of 16,16 dimethyl PGE2 (dmPGE2) on gastric acid secretion and back diffusion of H+ were studied in anaesthetised dogs which were prepared with a segment of the greater curvature of the stomach mounted in a double lumen chamber. This model permitted simultaneous evaluation of two segments of mucosa, one control and the other test, supplied by the same vascular pedicle. Imfusion of histamine (1.0 microgram/kg/min, intravenously) stimulated brisk acid secretion in both chambers. Topical application of 25 microgram dmPGE2 in 20 ml 0.3 M HC1 to the test chamber for 30 minutes prevented acid secretion from the test mucosa during a second histamine infusion. Since the control chamber showed no evidence of inhibition this indicates that dmPGE2 acted directly on the secretory cells, rather than after absorption from the bloodstream. This observation, however, does not exclude a possible local effect on mucosal blood flow. Direct exposure of the gastric mucosa to dmPGE2 increased the rate of back diffusion of H+ because of disruption of the permeability barrier, indicated by increased H+ back diffusion, Na+ efflux, and a reduction in potential difference. However, H+ loss was small compared to the reduction in acid output.

摘要

在麻醉犬身上研究了腔内滴注16,16 - 二甲基前列腺素E2(dmPGE2)对胃酸分泌和H⁺反向扩散的影响。这些犬制备了一段胃大弯,安装在双腔室中。该模型允许同时评估由同一血管蒂供应的两段黏膜,一段为对照,另一段为测试。静脉输注组胺(1.0微克/千克/分钟)刺激两个腔室快速分泌胃酸。在测试腔室中,将25微克dmPGE2加入20毫升0.3 M盐酸中,局部应用30分钟,可在第二次输注组胺期间阻止测试黏膜分泌胃酸。由于对照腔室未显示抑制迹象,这表明dmPGE2直接作用于分泌细胞,而非从血液中吸收后起作用。然而,这一观察结果并不排除对黏膜血流可能存在的局部影响。胃黏膜直接暴露于dmPGE2会增加H⁺反向扩散速率,这是由于通透性屏障被破坏,表现为H⁺反向扩散增加、Na⁺外流以及电位差降低。然而,与酸分泌量的减少相比,H⁺的损失较小。

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16,16-dimethyl PGE2 and HCO3- efflux.16,16 - 二甲基前列腺素E2与碳酸氢根外流
Dig Dis Sci. 1983 Jul;28(7):649-50. doi: 10.1007/BF01299926.

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