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本文引用的文献

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The influence of potassium and chloride ions on the membrane potential of single muscle fibres.钾离子和氯离子对单根肌纤维膜电位的影响。
J Physiol. 1959 Oct;148(1):127-60. doi: 10.1113/jphysiol.1959.sp006278.
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The action of calcium on the electrical properties of squid axons.钙对鱿鱼轴突电特性的作用。
J Physiol. 1957 Jul 11;137(2):218-44. doi: 10.1113/jphysiol.1957.sp005808.
3
Active chloride transport in the isolated toad bladder.离体蟾蜍膀胱中的活性氯转运
Am J Physiol. 1967 Jul;213(1):179-84. doi: 10.1152/ajplegacy.1967.213.1.179.
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Light-induced resistance changes in single photoreceptors of Necturus and Gekko.美西螈和壁虎单个光感受器中光诱导的电阻变化。
Vision Res. 1969 Apr;9(4):453-63. doi: 10.1016/0042-6989(69)90134-5.
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Receptive fields of cones in the retina of the turtle.海龟视网膜中视锥细胞的感受野。
J Physiol. 1971 Apr;214(2):265-94. doi: 10.1113/jphysiol.1971.sp009432.
6
Studies on the mass receptor potential of the isolated frog retina. II. On the basis of the ionic mechanism.离体蛙视网膜的群体感受器电位研究。II. 基于离子机制
Vision Res. 1969 Dec;9(12):1443-51. doi: 10.1016/0042-6989(69)90060-1.
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Electrophysiological study of the mechanisms subserving color coding in the fish retina.鱼类视网膜中颜色编码机制的电生理研究。
Cold Spring Harb Symp Quant Biol. 1965;30:559-66. doi: 10.1101/sqb.1965.030.01.054.
8
Inactivation of horizontal cells in turtle retina by glutamate and aspartate.谷氨酸和天冬氨酸对龟视网膜水平细胞的失活作用。
Science. 1972 Nov 17;178(4062):767-8. doi: 10.1126/science.178.4062.767.
9
Kinetics of the photocurrent of retinal rods.视网膜视杆细胞光电流的动力学
Biophys J. 1972 Aug;12(8):1073-94. doi: 10.1016/S0006-3495(72)86145-9.
10
The effects of intracellular iontophoretic injection of calcium and sodium ions on the light response of Limulus ventral photoreceptors.细胞内离子电渗法注射钙和钠离子对鲎腹侧光感受器光反应的影响。
J Gen Physiol. 1972 Jun;59(6):701-19. doi: 10.1085/jgp.59.6.701.

海蟾蜍视网膜光感受器电位的离子机制。

Ionic mechanism for the photoreceptor potential of the retina of Bufo marinus.

作者信息

Brown J E, Pinto L H

出版信息

J Physiol. 1974 Feb;236(3):575-91. doi: 10.1113/jphysiol.1974.sp010453.

DOI:10.1113/jphysiol.1974.sp010453
PMID:4207130
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1350850/
Abstract
  1. Membrane potentials were recorded from single rods in the isolated retina of Bufo marinus while the ionic composition of the extracellular medium was rapidly changed. Substitution of 2 mM aspartate(-) for Cl(-) produced a prompt depolarization of horizontal cells, but no modification of either resting potential or response to light in receptor cells. This implies that feed-back from horizontal cells to receptor cells was not active.2. During substitution of choline(+) or Li(+) for Na(+), and during isosmotic substitution of sucrose for NaCl, the resting potential of receptor cells became more negative and responses to light were abolished. During exposure to K(+)-free medium, the resting potential became slightly more negative and the responses to light became larger and developed small after-depolarizations. Exposure to K(+) of four times normal resulted in permanent diminution of response magnitude and permanent change of response waveshape. Removal of Mg(2+), four times normal Mg(2+) or substitution of methylsulphate(-) for Cl(-) had no effect on resting potential or responses to light. With the exception of the small effects seen with altered K(+) these results are consistent with the receptor potential being generated by a light-induced decrease of membrane conductance to Na(+).3. Exposure to decreased Ca(2+) caused both a depolarization of the receptor membrane in the dark and an increase in the magnitude of the maximal response that could be evoked by a test stimulus. The magnitude of the increase in response equalled the magnitude of the depolarization. Exposure to increased Ca(2+) or steady background light caused both a steady hyperpolarization and a decrease in the magnitude of the maximal response that could be evoked by a test stimulus. For steady hyperpolarizations greater than 3.5 mV, whether caused by elevated Ca(2+) or steady background light, the decrease in response magnitude exceeded the magnitude of the hyperpolarization. These results imply that externally applied Ca(2+) ions mimic the effects of steady background lights, but the applied Ca(2+) ions must do more than merely decrease membrane conductance to Na(+).
摘要
  1. 在快速改变细胞外介质离子组成的同时,记录了海蟾蜍离体视网膜中单个视杆细胞的膜电位。用2 mM天冬氨酸(-)替代Cl(-)可使水平细胞迅速去极化,但对感受器细胞的静息电位或光反应均无影响。这表明水平细胞向感受器细胞的反馈是不活跃的。

  2. 用胆碱(+)或Li(+)替代Na(+)期间,以及用蔗糖等渗替代NaCl期间,感受器细胞的静息电位变得更负,对光的反应消失。暴露于无K(+)培养基中时,静息电位略微变得更负,对光的反应变大并出现小的去极化后电位。暴露于四倍正常浓度的[K(+)](细胞外)会导致反应幅度永久性降低和反应波形永久性改变。去除Mg(2+)、四倍正常浓度的[Mg(2+)](细胞外)或用甲硫酸盐(-)替代Cl(-)对静息电位或光反应均无影响。除了[K(+)](细胞外)改变时观察到的微小影响外,这些结果与感受器电位是由光诱导的膜对Na(+)的电导降低所产生的观点一致。

  3. 暴露于降低的[Ca(2+)](细胞外)会导致暗处感受器膜去极化,并使测试刺激可诱发的最大反应幅度增加。反应增加的幅度等于去极化的幅度。暴露于增加的[Ca(2+)](细胞外)或稳定的背景光会导致稳定的超极化以及测试刺激可诱发的最大反应幅度降低。对于大于3.5 mV的稳定超极化,无论是由升高的[Ca(2+)](细胞外)还是稳定的背景光引起的,反应幅度的降低都超过了超极化的幅度。这些结果表明,外部施加的Ca(2+)离子模拟了稳定背景光的作用,但施加的Ca(2+)离子所起的作用必定不止于仅仅降低膜对Na(+)的电导。