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毫摩尔浓度的氨氯吡咪可阻断近端肾小管细胞的钾离子电导。

Millimolar amiloride concentrations block K conductance in proximal tubular cells.

作者信息

Discala F, Hulin P, Belachgar F, Planelles G, Edelman A, Anagnostopoulos T

机构信息

INSERM U. 323, Faculté de Médecine Necker Enfants-Malades, Paris, France.

出版信息

Br J Pharmacol. 1992 Oct;107(2):532-8. doi: 10.1111/j.1476-5381.1992.tb12779.x.

Abstract
  1. Amiloride, applied at millimolar concentrations, results in the blockade of K+ conductance in amphibian proximal convoluted cells (PCT), fused into giant cells. 2. Amiloride results directly in a blockade of K+ conductance that is not related to inhibition of the Na(+)-H+ antiport, which would lower intracellular pH, adversely affecting K+ conductance. On the contrary, high amiloride concentrations promote entry of this lipophilic base in the cell, leading to higher cell pH. 3. Under voltage clamp conditions, control vs. amiloride, current-voltage curves from PCT fused giant cells intersect at -86.2 +/- 3.4 mV, a value close to the equilibrium potential for potassium. 4. Hexamethylene amiloride, 10(-5) M, irreversibly depolarizes the membrane potential. 5. Barium decreased by 50% the initial slope of realkalinization, following removal of a solution containing NH4Cl, as did amiloride. In addition, these blockers reduced membrane conductance by 40%, suggesting that a fraction of the amiloride-suppressible NH4+ efflux may be conductive. 6. Amiloride does not directly inhibit the Na(+)-K+, ATPase in our preparation, contrary to the prevalent belief. 7. In vivo studies show that amiloride interferes with an apical K+ conductance but it does not alter basolateral K+ conductance.
摘要
  1. 以毫摩尔浓度应用的氨氯吡咪会导致融合成巨细胞的两栖动物近端曲管细胞(PCT)中的钾离子电导被阻断。2. 氨氯吡咪直接导致钾离子电导被阻断,这与抑制钠氢反向转运体无关,抑制钠氢反向转运体会降低细胞内pH值,对钾离子电导产生不利影响。相反,高浓度的氨氯吡咪会促进这种亲脂性碱进入细胞,导致细胞内pH值升高。3. 在电压钳制条件下,对照与氨氯吡咪处理的PCT融合巨细胞的电流-电压曲线在-86.2±3.4 mV处相交,该值接近钾离子的平衡电位。4. 10⁻⁵ M的六甲烯氨氯吡咪会使膜电位不可逆地去极化。5. 去除含氯化铵的溶液后,钡和氨氯吡咪一样,使再碱化的初始斜率降低了50%。此外,这些阻滞剂使膜电导降低了40%,这表明氨氯吡咪可抑制的一部分铵离子外流可能是有传导性的。6. 与普遍看法相反,在我们的实验制剂中,氨氯吡咪并不直接抑制钠钾ATP酶。7. 体内研究表明,氨氯吡咪会干扰顶端钾离子电导,但不会改变基底外侧钾离子电导。

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