首页> 外文期刊>Biological & pharmaceutical bulletin >Effects of progesterone and norethisterone on cephalexin transport and peptide transporter PEPT1 expression in human intestinal cell line Caco-2.
【24h】

Effects of progesterone and norethisterone on cephalexin transport and peptide transporter PEPT1 expression in human intestinal cell line Caco-2.

机译:孕酮和炔诺孕酮对人肠道细胞株Caco-2中头孢氨苄转运和肽转运子PEPT1表达的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

We investigated the effects of progesterone and norethisterone on the apical-to-basolateral and basolateral-to-apical transports of cephalexin, a typical peptide transporter PEPT1 substrate, and the PEPT1 mRNA and protein expression levels, using the human intestinal cell line, Caco-2. Caco-2 cell monolayers (passages 50 to 60) were cultured on permeable membrane, plastic culture dish and culture tube. The Caco-2 cell monolayers were pretreated with progesterone and norethisterone (3, 10, 30 microM) for 24 h. After the pretreatment, the apical-to-basolateral and basolateral-to-apical transports of cephalexin were measured, and the densities of PEPT1 mRNA and protein expression levels were analyzed by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot, respectively. The apical-to-basolateral transport of cephalexin was significantly decreased by the progesterone and norethisterone (30 microM each) pretreatments. By contrast, the basolateral-to-apical transport of cephalexin was not altered by the same pretreatments. The densities of PEPT1 mRNA and protein expressions were significantly decreased by progesterone and norethisterone (each at 3 and 10 microM) pretreatments compared with those of the non-treated Caco-2 cells. The results suggest that the transcription of the PEPT1 gene is downregulated by the progesterone and norethisterone pretreatments. Further studies are needed to clarify whether the inhibition of the PEPT1 gene transcription by progesterone pretreatment proceeds via sigma1-receptor or progesterone receptor.
机译:我们研究了黄体酮和炔诺孕酮对头孢氨苄从顶向基底外侧和基底外侧向顶转运的作用,一种典型的肽转运蛋白PEPT1底物,以及PEPT1 mRNA和蛋白质表达水平,使用了人类肠道细胞系Caco- 2。将Caco-2细胞单层(第50至60代)培养在可渗透膜,塑料培养皿和培养管上。用孕酮和炔诺酮(3、10、30 microM)预处理Caco-2细胞单层24 h。预处理后,测量头孢氨苄的顶向基底外侧和基底向顶转运,并通过逆转录聚合酶链反应(RT-PCR)和Western印迹分析PEPT1 mRNA的密度和蛋白表达水平,分别。孕酮和炔诺酮(各30 microM)预处理可显着降低头孢氨苄从顶向基底外侧的运输。相比之下,相同的预处理并未改变头孢氨苄的从基底外侧到顶端的转运。与未处理的Caco-2细胞相比,孕酮和炔诺酮(分别为3和10 microM)预处理可显着降低PEPT1 mRNA和蛋白表达的密度。结果表明,孕酮和炔诺酮预处理可下调PEPT1基因的转录。需要进一步的研究来阐明孕酮预处理对PEPT1基因转录的抑制是通过sigma1受体还是通过孕激素受体进行。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号