Watanabe Kazuhiro, Jinriki Toshiya, Sato Juichi
Hokkaido Pharmaceutical University, School of Pharmacy, Hokkaido, Japan.
Biol Pharm Bull. 2006 Jan;29(1):90-5. doi: 10.1248/bpb.29.90.
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.
我们使用人肠细胞系Caco-2,研究了孕酮和炔诺酮对头孢氨苄(一种典型的肽转运体PEPT1底物)从顶端到基底外侧以及从基底外侧到顶端转运的影响,以及对PEPT1 mRNA和蛋白表达水平的影响。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微摩尔)对Caco-2细胞单层进行预处理24小时。预处理后,测量头孢氨苄从顶端到基底外侧以及从基底外侧到顶端的转运,并分别通过逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法分析PEPT1 mRNA和蛋白表达水平的密度。孕酮和炔诺酮(各30微摩尔)预处理显著降低了头孢氨苄从顶端到基底外侧的转运。相比之下,相同的预处理并未改变头孢氨苄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(各3和10微摩尔)预处理显著降低了PEPT1 mRNA和蛋白表达的密度。结果表明,孕酮和炔诺酮预处理下调了PEPT1基因的转录。需要进一步研究以阐明孕酮预处理对PEPT1基因转录的抑制是否通过sigma1受体或孕酮受体进行。