Pinto L H, Ostroy S E
J Gen Physiol. 1978 Mar;71(3):329-45. doi: 10.1085/jgp.71.3.329.
The ionizable groups and conductances of the rod plasma membrane were studied by measuring membrane potential and input impedance with micropipettes that were placed in the rod outer segments. Reduction of the pH from 8.0 to 6.8 or from 7.8 to 7.3 resulted in membrane depolarization in the dark from 8.0 to 6.8 or from 7.8 to 7.3 resulted in membrane depolarization in the dark (by 2- 3 mV) and an increased size of the light response (also by 2-3 mV). The dark depolarization was accompanied by and increased resting input impedance (by 11-35 Momega). When the pH was decreased in a perfusate in which Cl(-) was replaced by isethionate, the membrane depolarized. When the pH was decreased in a perfusate in which Na(+) was replaced by choline, an increase of input impedance was observed (11-50 Momega) even though a depolarization did not occur. These results are consistent with the interpretation that the effects of decreased extracellular pH result mainly from a decrease in rod membrane K(+) conductance that is presumably cause by protonation of ionizable groups having a pK(a) between 7.3 and 7.8. Furthermore, from these results and results obtained by using CO(2) and NH(3) to affect specifically the internal pH of the cell, it seems unlikely that altered cytoplasmic [H(+)] is a cytoplasmic messenger for excitation of the rod. When the rods were exposed to perfusate in which Na(+) was replaced by choline, the resting (dark) input impedance increased (by 26 Momega +/- 5 Momega SE), and the light-induced changes in input impedance became undetectable. Replacement of Cl(-) by isethionate had no detectable effect on either the resting input impedance or the light-induced changes in input impedance. These results confirm previous findings that the primary effect of light is to decrease the membrane conductance to Na(+) and show that, if any other changes in conductance occur, they depend upon the change in Na(+) conductance. The results are consistent with the following relative resting conductances of the rod membrane: G(Na(+)) similar to G(K(+)) more than 2-5 G(Cl(-)).
通过将微电极置于视杆细胞外段来测量膜电位和输入阻抗,从而研究视杆细胞膜的可电离基团和电导。将pH从8.0降至6.8或从7.8降至7.3,会导致视杆细胞在黑暗中膜去极化(降低2 - 3 mV),同时光反应的幅度增加(也增加2 - 3 mV)。黑暗中的去极化伴随着静息输入阻抗的增加(增加11 - 35 MΩ)。当在灌流液中用羟乙基磺酸根取代Cl⁻时降低pH,膜会去极化。当在灌流液中用胆碱取代Na⁺时降低pH,尽管未发生去极化,但观察到输入阻抗增加(11 - 50 MΩ)。这些结果与以下解释一致:细胞外pH降低的影响主要源于视杆细胞膜K⁺电导的降低,这可能是由pK(a)在7.3至7.8之间的可电离基团质子化所致。此外,从这些结果以及通过使用CO₂和NH₃特异性影响细胞内pH所获得的结果来看,似乎细胞内[H⁺]的改变不太可能是视杆细胞兴奋的细胞内信使。当视杆细胞暴露于用胆碱取代Na⁺的灌流液中时,静息(黑暗)输入阻抗增加(增加26 MΩ±5 MΩ标准误),并且光诱导的输入阻抗变化变得无法检测到。用羟乙基磺酸根取代Cl⁻对静息输入阻抗或光诱导的输入阻抗变化均无明显影响。这些结果证实了先前的发现,即光的主要作用是降低膜对Na⁺的电导,并且表明,如果发生任何其他电导变化,它们取决于Na⁺电导的变化。结果与视杆细胞膜以下相对静息电导一致:G(Na⁺)≈G(K⁺)>2 - 5 G(Cl⁻)。