首页> 外文期刊>Clinical and experimental pharmacology & physiology >Regulation of 86Rb+ ion transport across polarized human colonocytes by bis-phenolic compounds.
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Regulation of 86Rb+ ion transport across polarized human colonocytes by bis-phenolic compounds.

机译:双酚化合物对极化人结肠细胞中86Rb +离子运输的调节。

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摘要

1. Phenolphthalein, a well-known laxative, stimulates the secretion of Na+ and Cl- ions and accompanying water into the intestinal tract. Measurement of 86Rb+ efflux from several, but not all, cell types indicates that phenolphthalein also results in release of cellular K+ ions. 2. In the present study, the transport of 86Rb+ across human colonocyte cells (T84) cultured on trans-well inserts was examined. The T84 cells were cultured until they developed tight junctions and a high trans-epithelial resistance. 3. Results show that phenolphthalein applied to the apical, but not the basolateral, surface of cells causes the release of 86Rb+ from the apical surface. Basolateral treatment of cells with phenolphthalein had no effect on the release of 86Rb+. 4. Simultaneously with the increased 86Rb+ efflux, indirect evidence of enhanced Na+/K+-ATPase activity was also observed. 5. Although ouabain inhibited the increased Na+ pump activity, it did not affect apical 86Rb+ release. 6. As evidenced by near steady state 86Rb+ uptake data, the increased Na+/K+-ATPase activity was insufficient to restore intracellular concentrations of K+ in the presence of phenolphthalein. 7. 4,4(9-Fluorenylidene)diphenol, a homologue of phenolphthalein, had a similar effect on 86Rb+ transport by T84 cells. 8. These results indicate a primary stimulation of 86Rb+ efflux from the apical surface of polarized T84 cells by apically applied bis-phenolic compounds. 9. A secondary stimulation of the basolateral Na+/K+-ATPase is thought to result from intracellular Na+ increase, as documented in several other cell types exposed to bis-phenolic compounds, although not directly measured in these experiments. 10. The results also indicate that bis-phenolic compounds interact specifically with some apical but not basolateral membrane structures in regulating 86Rb+ efflux from polarized T84 cells.
机译:1.酚酞,一种众所周知的泻药,刺激Na +和Cl-离子的分泌,并伴随水分进入肠道。对几种(但不是全部)细胞类型进行86Rb +外排的测量表明,酚酞还导致细胞K +离子的释放。 2.在本研究中,研究了86Rb +在跨孔插入物中培养的人类结肠细胞(T84)的转运。培养T84细胞,直到它们发展成紧密的连接和高的跨上皮抵抗力。 3.结果表明,酚酞应用于细胞的顶表面而不是基底外侧,引起从顶表面释放86Rb +。酚酞对细胞进行基底外侧处理对86Rb +的释放没有影响。 4.同时,随着86Rb +外排量的增加,也观察到Na + / K + -ATPase活性增强的间接证据。 5.尽管哇巴因抑制了Na +泵浦活动的增加,但它不影响根尖86Rb +的释放。 6.如接近稳定的86Rb +摄取数据所证明的,在酚酞存在下,增加的Na + / K + -ATPase活性不足以恢复细胞内K +的浓度。 7. 4,4(9-Fluorenylidene)diphenol,酚酞的同系物,对T84细胞的86Rb +转运具有相似的作用。 8.这些结果表明,顶端施用双酚类化合物可从极化T84细胞的顶端表面初步刺激86Rb +外流。 9.如在暴露于双酚类化合物的其他几种细胞类型中所记录的,尽管在这些实验中未直接测量,但据认为基底外侧Na + / K + -ATPase的二次刺激是由细胞内Na +的增加引起的。 10.结果还表明,双酚类化合物在调节极化T84细胞的86Rb +外排时,与某些顶端但不与基底外侧膜结构发生特异性相互作用。

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