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尿素抑制髓袢升支粗段细胞中的钠-钾-2氯协同转运。

Urea inhibits Na-K-2Cl cotransport in medullary thick ascending limb cells.

作者信息

Kaji D M, Diaz J, Parker J C

机构信息

Department of Medicine, Veterans Affairs Medical Center, Bronx, New York 10468, USA.

出版信息

Am J Physiol. 1997 Feb;272(2 Pt 1):C615-21. doi: 10.1152/ajpcell.1997.272.2.C615.

Abstract

We examined the effect of physiological concentrations of urea (100-500 mM) on Na-K-2Cl cotransport in cultured cells from mouse medullary thick ascending limb (mTAL). Urea acutely inhibited bumetanide-sensitive K influx in mTAL cells in a concentration-dependent fashion, with a statistically significant inhibition (19%) at 100 mM and 86% inhibition at 500 mM. The effect of urea was entirely reversible and was blocked by prior treatment with okadaic acid, a phosphatase inhibitor, suggesting that urea exerts its action upstream of the phosphorylation-dephosphorylation step. Cell volume was unchanged in the presence of 500 mM urea. The number of [3H]bumetanide binding sites, a measure of the number of functioning cotransporter sites, was decreased in the presence of urea, and the decrease in bumetanide binding was proportional to the decrease in bumetanide-sensitive K influx. Urea also stimulated the Ba-sensitive swelling-activated K efflux from mTAL cells. Thus urea, in concentrations that prevail in the renal medulla, alters ion transport in mTAL cells.

摘要

我们研究了生理浓度的尿素(100 - 500 mM)对从小鼠髓袢升支粗段(mTAL)培养的细胞中钠钾氯协同转运体的影响。尿素以浓度依赖的方式急性抑制mTAL细胞中布美他尼敏感的钾离子内流,在100 mM时具有统计学显著抑制作用(19%),在500 mM时抑制率达86%。尿素的作用完全可逆,且被磷酸酶抑制剂冈田酸预处理所阻断,这表明尿素在磷酸化 - 去磷酸化步骤的上游发挥作用。在500 mM尿素存在的情况下,细胞体积未发生变化。[3H]布美他尼结合位点的数量(衡量功能性协同转运体位点数量的指标)在尿素存在时减少,且布美他尼结合的减少与布美他尼敏感的钾离子内流的减少成比例。尿素还刺激了mTAL细胞中钡敏感的肿胀激活钾离子外流。因此,在肾髓质中占主导的浓度下,尿素会改变mTAL细胞中的离子转运。

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