Klemperer G, Essig A
Department of Physiology, Boston University School of Medicine, Massachusetts 02118.
J Membr Biol. 1988 Dec;106(2):107-18. doi: 10.1007/BF01871392.
The effects of serosal substitution of isosmotic Na2SO4-Ringer solution for NaCl-Ringer solution were studied in the short-circuited frog skin (Rana pipiens, Northern variety). Despite prompt changes of transepithelial measurements, initial cellular effects were slight. After 30 to 45 min, however, the transcellular current had decreased and the cell electrical potential had depolarized, in association with decrease of the apical membrane fractional resistance and basolateral membrane conductance. Apical membrane slope conductance was unaffected. Similar effects were obtained with isolated epithelia. With the use of gluconate or NO3 in place of Cl, the effects on cellular current and conductance were minimal or insignificant, despite changes of the cell potential, fractional resistance, and basolateral conductance similar to those seen with sulfate. Following prolonged exposure to serosal SO4-Ringer, the extent of depolarization induced by raising the serosal K concentration decreased, indicating diminution of basolateral K conductance and the existence of other basolateral conductances. Equilibration in serosal gluconate-Ringer enhanced polarization on serosal restoration of Cl or removal of Na, again indicating a time-dependent change in the basolateral conductance pattern. Depolarization on removal of serosal Cl was not attributable to inhibition of the pump. Nor was it the result of decrease of the K equilibrium potential EK: exposure to serosal SO4-Ringer decreased cell K activity aKc from 104 +/- 6 to 58 +/- 4 mM (n = 5), but EK was reduced only slightly; exposure to serosal gluconate increased aKc and EK. Serosal sulfate lowered the cell Na activity aNac, but the electrochemical potential difference for Na across the apical surface was unaffected. The concurrent decrease of both aKc and aNac following serosal substitution of SO4 for Cl raises questions concerning mechanisms of osmoregulation.
在短路的青蛙皮肤(北美豹蛙北方变种)中研究了用等渗Na₂SO₄-林格液替代NaCl-林格液对浆膜的影响。尽管跨上皮测量值迅速变化,但最初的细胞效应轻微。然而,30至45分钟后,跨细胞电流下降,细胞电势去极化,同时顶端膜分数电阻和基底外侧膜电导降低。顶端膜斜率电导未受影响。分离的上皮细胞也得到了类似的结果。用葡萄糖酸盐或NO₃代替Cl时,尽管细胞电势、分数电阻和基底外侧电导的变化与用硫酸盐时相似,但对细胞电流和电导的影响最小或不显著。长时间暴露于浆膜SO₄-林格液后,提高浆膜K浓度所诱导的去极化程度降低,表明基底外侧K电导减小,且存在其他基底外侧电导。在浆膜葡萄糖酸盐-林格液中平衡增强了在浆膜恢复Cl或去除Na时的极化,再次表明基底外侧电导模式存在时间依赖性变化。去除浆膜Cl时的去极化并非由于泵的抑制。也不是K平衡电位EK降低的结果:暴露于浆膜SO₄-林格液使细胞K活性aKc从104±6 mM降至58±4 mM(n = 5),但EK仅略有降低;暴露于浆膜葡萄糖酸盐使aKc和EK增加。浆膜硫酸盐降低了细胞Na活性aNac,但Na跨顶端表面的电化学势差未受影响。用SO₄替代Cl后浆膜中aKc和aNac同时降低,这引发了关于渗透调节机制的问题。