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一种新型的基于离子载体的双管氯离子微电极。

A new double-barrelled, ionophore-based microelectrode for chloride ions.

作者信息

Kondo Y, Bührer T, Seiler K, Frömter E, Simon W

机构信息

Zentrum der Physiologie, Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt, Federal Republic of Germany.

出版信息

Pflugers Arch. 1989 Sep;414(6):663-8. doi: 10.1007/BF00582133.

Abstract

A new Cl- selective microelectrode based on the ionophore 5,10,15,20-tetraphenyl-21H,23H-porphin manganese(III) chloride is presented which discriminates better against HCO3- and several organic anions than electrodes containing the Corning 477913 ion-exchanger. Using a redesigned construction procedure, fine-tip double-barrelled microelectrodes were produced which had slopes of -52.4 +/- 0.6 mV (SE, n = 24), resistances of about 7.10(11) omega and a selectivity coefficient log KpotCLHCO3 of -1.40 +/- 0.03. Some electrodes showed a small unexplained sensitivity to pH greater than 7.6. When used to puncture cells of isolated S3 segments of rabbit renal proximal tubule during perfusion with HCO3- Ringer solution, the electrodes gave a membrane potential of -69.8 +/- 1.5 mV and an intracellular Cl- activity, [Cl-]i, of 35.3 +/- 2.6 mmol/l. Upon switching bath and lumen perfusions to Cl- -free solutions the "residual" [Cl-]i dropped to 1.20 +/- 0.03 mmol/l, while in similar measurements with ion-exchanger electrodes the "residual" [Cl-]i dropped only to 10.9 +/- 0.5 mmol/l. These observations demonstrate the superiority of the new electrode and prove that previously determined high [Cl-]i values in Cl- -free ambient solutions reflect interference problems rather than non-exchangeable intracellular chloride.

摘要

本文介绍了一种基于离子载体5,10,15,20-四苯基-21H,23H-卟吩氯化锰(III)的新型氯离子选择性微电极,与含有康宁477913离子交换剂的电极相比,它对碳酸氢根离子和几种有机阴离子的区分能力更强。采用重新设计的制作工艺,制备出了细尖端双管微电极,其斜率为-52.4±0.6 mV(标准误,n = 24),电阻约为7×10¹¹Ω,选择性系数log KpotCLHCO3为-1.40±0.03。一些电极对pH大于7.6时表现出较小的无法解释的敏感性。当在灌注碳酸氢根林格溶液期间用于穿刺兔肾近端小管分离的S3节段细胞时,这些电极测得的膜电位为-69.8±1.5 mV,细胞内氯离子活性[Cl⁻]i为35.3±2.6 mmol/L。当将浴液和管腔灌注液换成无氯溶液时,“残余”[Cl⁻]i降至1.20±0.03 mmol/L,而在使用离子交换剂电极的类似测量中,“残余”[Cl⁻]i仅降至10.9±0.5 mmol/L。这些观察结果证明了新型电极的优越性,并证明了先前在无氯环境溶液中测定的高[Cl⁻]i值反映的是干扰问题,而非不可交换的细胞内氯离子。

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