Reuss L
J Gen Physiol. 1984 Sep;84(3):423-45. doi: 10.1085/jgp.84.3.423.
Transepithelial fluid transport (Jv) and intracellular Na+ and Cl- activities (aNai, aCli) were measured in isolated Necturus gallbladders to establish the contribution of different proposed apical membrane entry mechanisms to transepithelial salt transport. In 10 mM HCO3-Ringer's, Jv was 13.5 +/- 1.1 microliter X cm-2 X h-1, and was significantly reduced by a low bicarbonate medium and by addition of amiloride (10(-3)M) or SITS (0.5 X 10(-3)M) to the mucosal bathing solution. Bumetanide (10(-5)M) was ineffective. Bilateral Na+ removal abolished Jv. The hypothesis of NaCl cotransport was rejected on the basis of the following results, all obtained during mucosal bathing solution changes: during Na+ removal, aNai fell 4.3 times faster than aCli; during Cl- removal, aCli fell 7.5 times faster than aNai; amiloride (10(-3) M) reduced aNai at a rate of 2.4 +/- 0.3 mM/min, whereas aCli was not changed; bumetanide (10(-5) M) had no significant effects on Jv or aCli. The hypothesis of Na-K-Cl cotransport was rejected for the same reasons; in addition, K+ removal from the mucosal bathing solution (with concomitant Ba2+ addition) did not alter aNai or aCli. The average rate of NaCl entry under normal transporting conditions, estimated from Jv, assuming that the transported fluid is an isosmotic NaCl solution, was 22.5 nmol X cm-2 X min-1. Upon sudden cessation of NaCl entry, assuming no cell volume changes, aNai and aCli should fall at an average rate of 4.8 mM/min. To compare this rate with the rates of Na+ and Cl- entry by ion exchange, the Na+ or Cl- concentration in the mucosal bathing solution was reduced rapidly to levels such that electroneutral cation or anion exchange, respectively, should cease. The rate of Na+ or Cl- entry before this maneuver was estimated from the initial rate of fall of the respective intracellular ionic activity upon the mucosal solution substitution. aNai and aCli decreased at initial rates of 3.7 +/- 0.4 and 5.9 +/- 0.8 mM/min, respectively. The rate of fall of aNai upon reduction of external [Na] was not affected by amiloride (10(-3) M), and the rate of fall of aCli upon reduction of external [Cl] was unchanged by SITS (0.5 X 10(-3) M), which indicates that net cation or anion exchange was, in fact, abolished by the changes in Na+ and Cl- gradients, respectively. I conclude that double exchange (Na+/H+ and Cl-/HCO-3) is the predominant or sole mechanism of apical membrane NaCl entry in this epithelium.
在分离的美西螈胆囊中测量跨上皮液体转运(Jv)以及细胞内Na⁺和Cl⁻活性(aNai、aCli),以确定不同提出的顶端膜进入机制对跨上皮盐转运的贡献。在10 mM HCO₃ - 林格氏液中,Jv为13.5±1.1微升·厘米⁻²·小时⁻¹,低碳酸氢盐培养基以及向黏膜浴液中添加氨氯吡脒(10⁻³M)或SITS(0.5×10⁻³M)可使其显著降低。布美他尼(10⁻⁵M)无效。双侧去除Na⁺可消除Jv。基于以下所有在黏膜浴液变化期间获得的结果,NaCl共转运假说被否定:在去除Na⁺期间,aNai下降速度比aCli快4.3倍;在去除Cl⁻期间,aCli下降速度比aNai快7.5倍;氨氯吡脒(10⁻³M)使aNai以2.4±0.3 mM/分钟的速率降低,而aCli未改变;布美他尼(10⁻⁵M)对Jv或aCli无显著影响。由于相同原因,Na - K - Cl共转运假说也被否定;此外,从黏膜浴液中去除K⁺(同时添加Ba²⁺)并未改变aNai或aCli。在正常转运条件下,假设转运的液体是等渗NaCl溶液,根据Jv估算的NaCl进入平均速率为22.5 nmol·厘米⁻²·分钟⁻¹。在NaCl进入突然停止时,假设细胞体积不变,aNai和aCli应平均以4.8 mM/分钟的速率下降。为了将该速率与通过离子交换的Na⁺和Cl⁻进入速率进行比较,将黏膜浴液中的Na⁺或Cl⁻浓度迅速降低至分别应停止电中性阳离子或阴离子交换的水平。在此操作之前,根据黏膜溶液替换后各自细胞内离子活性的初始下降速率估算Na⁺或Cl⁻进入速率。aNai和aCli分别以3.7±0.4和5.9±0.8 mM/分钟的初始速率下降。降低外部[Na]时aNai的下降速率不受氨氯吡脒(10⁻³M)影响,降低外部[Cl]时aCli的下降速率不受SITS(0.5×10⁻³M)影响,这表明实际上分别通过Na⁺和Cl⁻梯度的变化消除了净阳离子或阴离子交换。我得出结论,双重交换(Na⁺/H⁺和Cl⁻/HCO₃⁻)是该上皮细胞顶端膜NaCl进入的主要或唯一机制。