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泻药对人体直肠跨黏膜电位差的影响。

The effect of cathartic agents on transmucosal electrical potential difference in the human rectum.

作者信息

Ewe K, Wanitschke R

出版信息

Klin Wochenschr. 1980 Mar 17;58(6):299-306. doi: 10.1007/BF01476572.

Abstract

Active ion transport in the colon is generating a transmucosal electrical potential difference (PD) of about 40 mV. Cathartic agents inhibit electrolyte and water net-absorption or cause net-secretion which should be reflected in a change of PD. In 83 normal subjects the effect of an isotonic eletrolyte solution (control) and different cathartic agents on rectal PD was tested: Laxatives (bisacodyl, rhein), bile acids (cholic and deoxycholic acid), fatty acids (oleic and ricinoleic acid) and cardiac glycosides (meproscillarin, digitoxin, digoxin). Bisacodyl, deoxycholic acid in high concentration, meproscillarin and digitoxin significantly decreased PD, while the other substances did not. Cathartics act on different transport mechanisms which together with different absorption characteristics of the proximal and distal colon may explain the difference in effecting the PD. Rectal PD measurement provides an easy and convenient tool to document effects of cathartic agents on electrolyte transport, otherwise difficult to obtain, and is applicable for clinical use.

摘要

结肠中的主动离子转运正在产生约40 mV的跨粘膜电位差(PD)。泻药抑制电解质和水的净吸收或引起净分泌,这应反映在PD的变化中。在83名正常受试者中,测试了等渗电解质溶液(对照)和不同泻药对直肠PD的影响:泻药(比沙可啶、大黄酸)、胆汁酸(胆酸和脱氧胆酸)、脂肪酸(油酸和蓖麻油酸)和强心苷(甲丙氨酯洋地黄毒苷、地高辛、洋地黄毒苷)。比沙可啶、高浓度的脱氧胆酸、甲丙氨酯洋地黄毒苷和洋地黄毒苷显著降低了PD,而其他物质则没有。泻药作用于不同的转运机制,这与近端和远端结肠不同的吸收特性一起,可能解释了对PD影响的差异。直肠PD测量提供了一种简单方便的工具,用于记录泻药对电解质转运的影响,否则难以获得,并且适用于临床使用。

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