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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Downregulation of Aquaporin 3 Mediated the Laxative Effect in the Rat Colon by a Purified Resin Glycoside Fraction from Pharbitis Semen
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Downregulation of Aquaporin 3 Mediated the Laxative Effect in the Rat Colon by a Purified Resin Glycoside Fraction from Pharbitis Semen

机译:Aquaporin 3的下调介导通过纯化的树脂糖苷馏分从肺炎精液中介导大鼠结肠中的泻药作用

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Background. Pharbitis Semen, the seeds of Pharbitis nil, is widely used as a traditional purgative medicine in China, Korea, and Japan. This study investigated the laxative effects of a purified resin glycoside fraction obtained in our previous study from Pharbitis Semen in vivo and in vitro. Materials and Methods. After orally administering a purified resin glycoside fraction from Pharbitis Semen (RFP) to rats, the content of fecal water, AQP3, NF-B, COX-2 expression, and the prostaglandin E-2 (PGE(2)) concentrations in the colon were examined. Moreover, human intestinal epithelial cells (HT-29) were used to investigate the mechanism of RFP decreasing the AQP3 expression. Results. Results obtained showed that treatment with RFP increased the feces excretion and fecal water content of rats in a dose-dependent manner. More interestingly, AQP3 expression was suppressed by RFP treatment both in the rat colons and in HT-29 cells, while the NF-B pathway-mediated PGE(2) production was activated. Interestingly, pretreating rats with BAY-11-7082 (NF-B inhibitor) or indomethacin (COX-2 inhibitor) and RFP neither induced diarrhea nor decreased the AQP3 expression in the colon. Conclusions. The purgative property of the purified resin glycoside fraction was attributed to NF-B activation in the colon, which increased the COX-2-mediated secretion of PGE(2). PGE(2) decreased AQP3 expression which inhibits water absorbed from the intestine to the blood vessel side, resulting in the laxative effect of RFP.
机译:背景。 Pharbitis精液,植物炎的种子,广泛用作中国,韩国和日本的传统泻药。该研究研究了在我们以前的研究中获得的纯化树脂糖苷级分的泻药效应从体内和体内测定的Pharbisitis精液中获得的。材料和方法。在口服从肺炎精液(RFP)对大鼠的纯化树脂糖苷馏分后,粪便水,AQP3,NF-B,COX-2表达和前列腺素E-2(PGE(2))浓度的含量检查了。此外,人肠上皮细胞(HT-29)用于研究RFP降低AQP3表达的机制。结果。得到的结果表明,用剂量依赖性方式增加RFP的治疗增加了大鼠的粪便排泄和粪便含水量。更有趣的是,在大鼠冒号和HT-29细胞中,RFP治疗抑制了AQP3表达,而NF-B途径介导的PGE(2)产生被激活。有趣的是,用Bay-11-7082(NF-B抑制剂)或吲哚美辛(COX-2抑制剂)和RFP的预处理大鼠既没有诱导腹泻,也没有降低结肠中的AQP3表达。结论。纯化的树脂糖苷级分的泻药属性归因于结肠中的NF-B活化,其增加了PGE(2)的COX-2介导的分泌。 PGE(2)降低了AQP3表达,其抑制从肠道吸收到血管侧的水,导致RFP的泻药作用。

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