Kubokawa M, Mori Y, Fujimoto K, Kubota T
Department of Physiology, Osaka Medical College, Takatsuki, Japan.
Jpn J Physiol. 1998 Feb;48(1):1-8. doi: 10.2170/jjphysiol.48.1.
The present study investigated basolateral K+ channels and their pH-sensitivity in isolated bullfrog proximal tubule cells by using the patch-clamp technique, and compared channel activity with the basolateral membrane potential (EM) and intracellular pH (pHi) monitored by using double-barreled H+-selective microelectrodes in perfused bullfrog proximal tubules. In the patch-clamp experiments, K+ channels with inward slope conductance of about 50 pS were observed in the basolateral membrane of isolated proximal tubule cells in cell-attached patches. Raising pH of the bath with HCO3(-)-free HEPES Ringer solutions from 7.7 (control) to 8.2 in the presence of an H+ ionophore, FCCP (2 micro M), enhanced channel activity to 126.4% of controls; lowering bath pH to 7.2 and to 6.7 reduced channel activity to 26.4 and to 1.7% of controls. Microelectrode experiments in bullfrog proximal tubules perfused with HCO3(-) -free HEPES Ringer solutions showed that EM and pHi in control conditions of peritubular pH 7.7 without FCCP were -52.6 mV and 7.45. Raising peritubular pH to 8.2 in the presence of FCCP (2 micro M) increased EM and pHi to -61.8 mV and 7.73; lowering it to 7. 2 and to 6.7 decreased EM and pHi to -28.6 mV and 7.25 and to -10.6 mV and 6.95. These results suggest that changes in EM in response to cellular alkalinization or acidification made by HCO3(-)-free HEPES solutions are produced primarily by changes in activity of the pH-sensitive K+ channels.
本研究采用膜片钳技术,对分离的牛蛙近端小管细胞中的基底外侧钾通道及其pH敏感性进行了研究,并将通道活性与灌注牛蛙近端小管中使用双管H⁺选择性微电极监测的基底外侧膜电位(EM)和细胞内pH(pHi)进行了比较。在膜片钳实验中,在细胞贴附式膜片中,分离的近端小管细胞基底外侧膜中观察到内向斜率电导约为50 pS的钾通道。在存在H⁺离子载体羰基氰化物间氯苯腙(FCCP,2 μM)的情况下,用不含HCO₃⁻的HEPES林格液将浴液pH从7.7(对照)提高到8.2,可使通道活性增强至对照的126.4%;将浴液pH降低至7.2和6.7可使通道活性分别降低至对照的26.4%和1.7%。用不含HCO₃⁻的HEPES林格液灌注牛蛙近端小管的微电极实验表明,在无FCCP的情况下,管周pH 7.7的对照条件下,EM和pHi分别为-52.6 mV和7.45。在存在FCCP(2 μM)的情况下将管周pH提高到8.2,可使EM和pHi分别升高至-61.8 mV和7.73;将其降低至7.2和6.7可使EM和pHi分别降低至-28.6 mV和7.25以及-10.6 mV和6.95。这些结果表明,由不含HCO₃⁻的HEPES溶液引起的细胞碱化或酸化所导致的EM变化,主要是由pH敏感钾通道活性的变化引起的。