首页> 美国卫生研究院文献>The Journal of General Physiology >Electrical and adaptive properties of rod photoreceptors in bufo marinus. I. Effects of altered extracellular Ca(2+) levels
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Electrical and adaptive properties of rod photoreceptors in bufo marinus. I. Effects of altered extracellular Ca(2+) levels

机译:中华大蟾蜍杆状光感受器的电学和适应性。 I.改变细胞外Ca(2+)水平的影响

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摘要

The effects of altering extracellular Ca(2+) levels on the electrical and adaptive properties of toad rods have been examined. The retina was continually superfused in control (1.6 mM Ca(2+)) or test ringer’s solutions, and rod electrical activity was recorded intracellularly. Low-calcium ringer’s (10(-9)M Ca(2+)) superfused for up to 6 min caused a substantial depolarization of the resting membrane potential, an increase in light-evoked response amplitudes, and a change in the waveform of the light-evoked responses. High Ca(2+) ringer’s (3.2 mM) hyperpolarized the cell membrane and decreased response amplitudes. However, under conditions of either low or high Ca(2+) superfusion for up to 6 min, in both dark-adapted and partially light-adapted states, receptor sensitivity was virtually unaffected; i.e., the V-log I curve for the receptor potential was always located on the intensity scale at a position predicted by the prevailing light level, not by Ca(2+) concentration. Thus, we speculate that cytosol Ca(2+) concentration is capable of regulating membrane potential levels and light-evoked response amplitudes, but not the major component of rod sensitivity. Low Ca(2+) ringer’s also shortened the period of receptor response saturation after a bright but nonbleaching light flash, hence accelerating the onset of both membrane potential and sensitivity recovery during dark adaptation. Exposure of the retina to low Ca(2+) (10(-9)M) ringer’s for long periods (7-15 min) caused dark-adapted rods to lose responsiveness. Response amplitudes gradually decreased, and the rods became desensitized. These severe conditions of low Ca(2+) caused changes in the dark-adapted rod that mimic those observed in rods during light adaptation. We suggest that loss of receptor sensitivity during prolonged exposure to low Ca(2+) ringer’s results from a decrease of intracellular (intradisk) stores of Ca(2+); i.e., less Ca(2+) is thereby released per quantum catch.
机译:已经检查了改变细胞外Ca(2+)水平对蟾蜍棒的电学和适应性特性的影响。视网膜在对照(1.6 mM Ca(2+))或测试林格氏液中持续灌注,并在细胞内记录了棒的电活动。低钙林格氏(10(-9)M Ca(2+))融合长达6分钟导致静息膜电位大量去极化,光诱发反应幅度增加以及波形的变化诱发反应。高Ca(2+)林格氏(3.2 mM)使细胞膜超极化,并降低了响应幅度。然而,在低或高Ca(2+)灌注长达6分钟的条件下,在黑暗适应和部分光照适应状态下,受体敏感性实际上均不受影响;即,受体电位的V-log I曲线始终位于强度标度上,该强度标度由主要光线水平而不是由Ca(2+)浓度预测。因此,我们推测胞质Ca(2+)的浓度能够调节膜电位水平和光诱发反应幅度,但不是杆灵敏度的主要组成部分。低Ca(2+)振铃剂还缩短了明亮但不漂白的闪光后的受体反应饱和的时间,因此加快了暗适应过程中膜电位和敏感性恢复的开始。长时间(7-15分钟)使视网膜暴露于低Ca(2+)(10(-9)M)振铃器会导致暗适应的视杆丧失反应能力。响应幅度逐渐降低,并且杆变得不敏感。这些严重的低Ca(2+)状况导致暗适应杆的变化,模仿了光适应过程中在杆中观察到的变化。我们建议长时间暴露于低Ca(2+)林格的过程中受体敏感性的降低是由于Ca(2+)的细胞内(盘内)存储减少所致;也就是说,每个量子捕获释放出更少的Ca(2+)。

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