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利用细胞内氯离子和pH敏感微电极研究静息绵羊心脏浦肯野纤维中氯离子的调节。

Regulation of chloride in quiescent sheep-heart Purkinje fibres studied using intracellular chloride and pH-sensitive micro-electrodes.

作者信息

Vaughan-Jones R D

出版信息

J Physiol. 1979 Oct;295:111-37. doi: 10.1113/jphysiol.1979.sp012957.

Abstract
  1. The intracellular Cl activity, alpha iCl was measured inside quiescent sheep cardiac Purkinje fibres, bathed in normal Tyrode at pH 7.40, buffered with approximately 22 mM-bicarbonate/approximately 5% CO2 + 95% O2. The measurements were made using liquid ion-exchanger Cl-sensitive micro-electrodes. 2. After internal Cl levels had been depleted by prolonged exposure to Cl-free media (glururonate-substituted) when external Cl was restored, there was a rapid re-accumulation of Cl inside the fibres to levels that were much higher than those expected for a passive Cl distribution. Such a process can be conveniently defined as an active inward Cl pump. 3. The inward-pumping was noticeably temperature-sensitive (Q10 approximately 2.6), its rate was reduced about eighteenfold in the nominal absence of external bicarbonate/CO2 and it was substantially inhibited by the drug SITS (4-acetamido-4'-isothiocyanato-stilbene-2,2'-disulphonic acid). 4. The fall of alpha iCl in Cl-free solution was slow and was also equally temperature-sensitive and substantially inhibited by SITS, but was only slightly impaired in the nominal absence of external bicarbonate/CO2. 5. pHi was measured using recessed-tip pH-sensitive micro-electrodes, and in some experiments both pHi and alpha iCl were monitored simultaneously. When alpha iCl slowly declined in Cl-free solution then pHi slowly became alkaline. Upon restoring external Cl, then there was, as usual, a rapid recovery of a high alpha iCl and this was accompanied by a rapid re-acidification of pHi. Both the recovery of alpha iCl and pHi were exponential with virtually the same time constant. 6. Both the slow alkalinization of pHi in Cl-free solution and the rapid re-acidification upon restoring external Cl were substantially inhibited by the drug SITS. 7. When [k]O was raised to 45 mM or more (by removing equivalent amounts of [Na]O), there was a large depolarization of Em and a slow rise of alpha iCl, which was not accompanied by a large change of pHi. The rise of alpha iCl appeared to be unaffected by SITS. 8. It is suggested that a Cl/CHO-3 exchange mechanism can operate reversibly across the membrane of quiescent Purkinje fibres, and that it can account, at least in part, for the high levels of alpha iCl measured in the resting state. It is also concluded that Cl can cross the membrane in other ways, especially in high-K solution possibly by moving passively through conductance channels that are open under these conditions.
摘要
  1. 在pH 7.40的正常台氏液中,用约22 mM碳酸氢盐/约5%二氧化碳+95%氧气缓冲,对静息状态的绵羊心脏浦肯野纤维内部的细胞内氯离子活性(αiCl)进行测量。测量使用液体离子交换剂氯离子敏感微电极。2. 在长时间暴露于无氯培养基(葡萄糖醛酸盐替代)使内部氯离子水平耗尽后,恢复外部氯离子时,纤维内部的氯离子迅速重新积累至远高于被动氯离子分布预期的水平。这样一个过程可方便地定义为主动内向氯离子泵。3. 内向泵明显对温度敏感(Q10约为2.6),在名义上无外部碳酸氢盐/二氧化碳时其速率降低约18倍,且被药物SITS(4-乙酰氨基-4'-异硫氰酸基芪-2,2'-二磺酸)显著抑制。4. 在无氯溶液中αiCl的下降缓慢,同样对温度敏感且被SITS显著抑制,但在名义上无外部碳酸氢盐/二氧化碳时仅略有受损。5. 使用凹陷尖端pH敏感微电极测量细胞内pH(pHi),在一些实验中同时监测pHi和αiCl。当αiCl在无氯溶液中缓慢下降时,pHi缓慢变为碱性。恢复外部氯离子后,如往常一样,αiCl迅速恢复到高水平,同时伴随着pHi的迅速再酸化。αiCl和pHi的恢复均呈指数形式,时间常数基本相同。6. 无氯溶液中pHi的缓慢碱化以及恢复外部氯离子时的迅速再酸化均被药物SITS显著抑制。7. 当细胞外钾离子浓度([k]O)升高至45 mM或更高(通过去除等量的细胞外钠离子([Na]O))时,膜电位(Em)出现大幅去极化,αiCl缓慢上升,且pHi无大幅变化。αiCl的上升似乎不受SITS影响。8. 提示氯离子/碳酸氢根离子交换机制可在静息浦肯野纤维膜上可逆运行,且至少部分可解释静息状态下测得的高αiCl水平。还得出结论,氯离子可通过其他方式穿过膜,尤其是在高钾溶液中,可能是通过在这些条件下开放的电导通道被动移动。

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