Ehrenfeld J, Cragoe E J, Harvey B J
Pflugers Arch. 1987 Jun;409(1-2):200-7. doi: 10.1007/BF00584772.
We have investigated the possible existence of a Na+/H+ ion exchanger in the frog skin epithelium by using isotopic methods and two amiloride analogues:5-(N-ethyl-N-isopropyl)-amiloride (EIPA) and phenamil. We found phenamil to be a specific blocker of sodium entry to its cellular transport compartment since it inhibited both the transepithelial Na+ influxes (J13) with a K1 of 4 X 10(-7) mol/l and the Na+ pool (control: 77 +/- 4 neq X h-1 X cm-2; phenamil: 21 +/- 1 neq X h-1 X cm-2). On the contrary EIPA (10(-5) mol/l) had no effect on J13 nor on the apical Na+ conductance. Acidification of the epithelium by passing from a normal Ringer (25 mmol/l HCO3-, 5% CO2, pH 7.34) to a HCO3(-)-free Ringer (5% CO2, pH 6.20) while blocking the Na+ conductance with phenamil, produced a large stimulation of Na+ influxes exclusively across the basolateral membranes (J32), after return to a normal Ringer (J32 = 706 +/- 76 and 1635 +/- 199 neq X h-1 X cm-2 in control and acid-loaded epithelia respectively). The stimulation of J32 was initiated when the epithelia were acid-loaded with Ringer of pH lower than 6.90 and was blocked by amiloride (KI = 7 X 10(-6) mol/l) and EIPA (KI = 5 X 10(-7) mol/l) whereas phenamil had no effect. In Na+-loaded epithelia (ouabain treated) the Na+ efflux across the basolateral membranes was stimulated by an inwardly directed proton gradient and was blocked by EIPA (10(-5) mol/l) or amiloride (10(-4) mol/l), a result suggesting reversibility of the mechanism. We conclude that a Na+ permeability mediated by a Na+/H+ ion exchanger exists in the basolateral membranes, which is stimulated by intracellular acidification and is sensitive to amiloride or EIPA. This exchanger is proposed to be involved in intracellular pH regulation.
5-(N-乙基-N-异丙基)-氨氯吡脒(EIPA)和非那明,研究了蛙皮上皮细胞中Na⁺/H⁺离子交换体可能的存在情况。我们发现非那明是钠进入其细胞转运区室的特异性阻滞剂,因为它抑制了跨上皮Na⁺内流(J13),其抑制常数K1为4×10⁻⁷mol/L,同时也抑制了Na⁺池(对照:77±4纳摩尔×小时⁻¹×厘米⁻²;非那明:21±1纳摩尔×小时⁻¹×厘米⁻²)。相反,EIPA(10⁻⁵mol/L)对J13和顶端Na⁺电导均无影响。当从正常林格液(25mmol/L HCO₃⁻,5% CO₂,pH 7.34)转变为无HCO₃⁻的林格液(5% CO₂,pH 6.20)使上皮细胞酸化,同时用非那明阻断Na⁺电导时,在恢复到正常林格液后,仅通过基底外侧膜产生了对Na⁺内流的大幅刺激(J32)(对照和酸负荷上皮细胞中J32分别为706±76和1635±199纳摩尔×小时⁻¹×厘米⁻²)。当上皮细胞用pH低于6.90的林格液进行酸负荷时,J32的刺激开始,并被氨氯吡脒(KI = 7×10⁻⁶mol/L)和EIPA(KI = 5×10⁻⁷mol/L)阻断,而非那明则无作用。在Na⁺负荷的上皮细胞(哇巴因处理)中,通过基底外侧膜的Na⁺外流受到内向质子梯度的刺激,并被EIPA(10⁻⁵mol/L)或氨氯吡脒(10⁻⁴mol/L)阻断,这一结果表明该机制具有可逆性。我们得出结论,基底外侧膜中存在由Na⁺/H⁺离子交换体介导的Na⁺通透性,它受到细胞内酸化的刺激,并且对氨氯吡脒或EIPA敏感。该交换体被认为参与细胞内pH调节。