Jacobsen C, Røigaard-Petersen H, Sheikh M I
Institute of Medical Biochemistry, University of Aarhus, Denmark.
FEBS Lett. 1988 Aug 15;236(1):95-9. doi: 10.1016/0014-5793(88)80292-8.
Characteristics of 22Na+ fluxes through Na+ channels in luminal-membrane vesicles isolated from either pars recta or pars convoluta of rabbit proximal tubule were studied. In NaCl-loaded vesicles from pars recta, transient accumulation of 22Na+ is observed, which is inhibited by amiloride. The isotope accumulation is driven by an electrical diffusion potential as shown in experiments using either these membrane vesicles loaded with different anions, or an outwardly directed K+ gradient with a K+ ionophore valinomycin. The vesicles containing the channel show a cation selectivity with the order Li+ greater than Na+ greater than K+. The amiloride-sensitive 22Na+ flux is dependent on intravesicular Ca2+. In NaCl-loaded vesicles from pars convoluta, no overshoot for 22Na+ uptake is observed. Furthermore, addition of amiloride to the incubation medium did not influence the uptake of 22Na+ in these vesicle preparations. It is concluded that Na+ channels are only present in pars recta of rabbit proximal tubule.
对从兔近端小管直部或曲部分离的管腔膜囊泡中通过钠离子通道的22Na+通量特性进行了研究。在来自直部的装载氯化钠的囊泡中,观察到22Na+的瞬时积累,其被氨氯吡脒抑制。同位素积累由电扩散电位驱动,如使用装载不同阴离子的这些膜囊泡或用钾离子载体缬氨霉素形成外向钾离子梯度的实验所示。含有该通道的囊泡表现出阳离子选择性,顺序为Li+>Na+>K+。氨氯吡脒敏感的22Na+通量依赖于囊泡内的Ca2+。在来自曲部的装载氯化钠的囊泡中,未观察到22Na+摄取的过冲现象。此外,向孵育培养基中添加氨氯吡脒并不影响这些囊泡制剂中22Na+的摄取。得出的结论是,钠离子通道仅存在于兔近端小管的直部。