Raynauld J P, Laviolette J R
J Neurosci Methods. 1987 Mar;19(3):249-55. doi: 10.1016/s0165-0270(87)80009-2.
Large input currents can be generated by an asymmetry in the chloride activity seen by Ag-AgCl electrodes used at the input of intracellular amplifiers because offset compensation no longer takes place at the input of the amplifier but rather later in the circuit in many modern amplifiers. This situation occurs when chloride-free solution, such as potassium acetate, potassium citrate or various intracellular dyes are used as pipette and electrode holder filling solutions. Omitting the agar bridge at the reference electrode, or using a platinum electrode will have similar results. Values of cellular membrane potentials can be significantly contaminated under such conditions, particularly where the amplifier input resistance did not exceed 10(10) omega and where small cells were studied. Unexpected iontophoresis of Cl- can occur when the asymmetry is such as to make the recording pipette negative. These offsets can be avoided in all situations by the use of salt bridges which insure that the two Ag/AgCl junctions are in contact with Cl- of the same activity.
在细胞内放大器输入端使用的银-氯化银电极所感知的氯离子活性不对称时,会产生大的输入电流,因为在许多现代放大器中,失调补偿不再在放大器输入端进行,而是在电路的后续部分进行。当使用无氯溶液(如醋酸钾、柠檬酸钾或各种细胞内染料)作为移液管和电极支架填充溶液时,就会出现这种情况。省略参比电极处的琼脂桥或使用铂电极也会有类似结果。在这种情况下,细胞膜电位值可能会受到显著污染,特别是在放大器输入电阻不超过10¹⁰Ω且研究的是小细胞时。当不对称性使得记录移液管带负电时,可能会发生意外的氯离子离子电泳。在所有情况下,通过使用盐桥可以避免这些失调,盐桥可确保两个银/氯化银结与具有相同活性的氯离子接触。