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比沙可啶的通便作用归因于巨噬细胞分泌的 PGE2 增加导致结肠中水通道蛋白-3 的表达减少。

The laxative effect of bisacodyl is attributable to decreased aquaporin-3 expression in the colon induced by increased PGE2 secretion from macrophages.

机构信息

Department of Clinical Pharmacokinetics, Hoshi University, Tokyo, Japan.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2011 Nov;301(5):G887-95. doi: 10.1152/ajpgi.00286.2011. Epub 2011 Aug 25.

Abstract

The purpose of this study was to investigate the role of aquaporin3 (AQP3) in the colon in the laxative effect of bisacodyl. After oral administration of bisacodyl to rats, AQP3, macrophages, cyclooxygenase 2 (COX2), and prostaglandin E(2) (PGE(2)) were examined in the colon. The mechanism by which bisacodyl decreases the expression of AQP3 was examined using HT-29 and Raw264.7 cells. When diarrhea occurred, a significant increase in the expression of PGE(2) and a decrease in AQP3 expression were observed. Immunostaining showed COX2 expression only in macrophages. The PGE(2) concentration increased significantly 30 min after the addition of bisacodyl to Raw264.7 cells. Thirty minutes after PGE(2) addition to HT-29 cells, the AQP3 expression level decreased to 40% of the control. When pretreated with indomethacin, bisacodyl did not induce an increase in the colon PGE(2) level, a decrease in the AQP3 expression level, or diarrhea. The results suggest that bisacodyl may decrease the expression of AQP3 in the colon, which inhibits water transfer from the luminal to the vascular side and leads to a laxative effect. This study also showed that direct activation of colon macrophages by bisacodyl increases the secretion of PGE(2), which acts as a paracrine factor and decreases AQP3 expression in colon mucosal epithelial cells.

摘要

本研究旨在探讨水通道蛋白 3(AQP3)在结肠中在比沙可啶通便作用中的作用。大鼠口服比沙可啶后,检测结肠中的 AQP3、巨噬细胞、环氧化酶 2(COX2)和前列腺素 E2(PGE2)。使用 HT-29 和 Raw264.7 细胞研究比沙可啶降低 AQP3 表达的机制。当发生腹泻时,观察到 PGE2 的表达显著增加,而 AQP3 的表达减少。免疫染色仅显示 COX2 在巨噬细胞中表达。向 Raw264.7 细胞中加入比沙可啶 30 分钟后,PGE2 浓度显著增加。向 HT-29 细胞中加入 PGE2 30 分钟后,AQP3 的表达水平降至对照的 40%。用吲哚美辛预处理时,比沙可啶不会诱导结肠 PGE2 水平升高、AQP3 表达水平降低或腹泻。结果表明,比沙可啶可能会降低结肠中 AQP3 的表达,从而抑制水从腔内向血管侧的转移,导致通便作用。本研究还表明,比沙可啶直接激活结肠巨噬细胞会增加 PGE2 的分泌,作为旁分泌因子,降低结肠黏膜上皮细胞中的 AQP3 表达。

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