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电生性钠钾泵对蟾蜍视杆细胞电活动的作用。

The contribution of the electrogenic sodium-potassium pump to the electrical activity of toad rods.

作者信息

Torre V

出版信息

J Physiol. 1982 Dec;333:315-41. doi: 10.1113/jphysiol.1982.sp014456.

Abstract
  1. The membrane potential of rods in the isolated toad retina was recorded while changing the ionic composition of the extracellular medium.2. Caesium (Cs(+)) at a concentration of 1 mM was sufficient to completely block the sag from the peak to the plateau in the bright-flash voltage response.3. In the presence of 10 mM-Cs(+) the bright-flash response increased in amplitude to about 90 mV, thus reaching an absolute membrane potential of between -110 and -135 mV. These responses consisted of an initial fast component of about 35 mV followed by a much slower component which could be as large as 50 mV.4. At the peak of the initial fast component the rod membrane conformed closely to the behaviour of a K(+) electrode with a P(Na)/P(K) ratio of 0.023. On average the amplitude of the slow component was about 35 mV in the presence of 2.6 mM-K(+) and was reduced to about 25 mV in a K(+)-free Ringer.5. Addition of 100 muM-strophanthidin to the perfusate induced several reversible changes in the electrical activity of rods. The dark resting membrane potential depolarized by about 5 mV and the kinetics of the voltage response to dim flashes of light slowed down. The voltage sensitivity initially increased by about 30%, but the peak of the response to a bright flash of light was reduced by about 13 mV.6. In rods treated with 10 mM-Cs(+) the slow component present in the bright flash response was abolished by strophanthidin with an apparent K(m) of 3 muM.7. The amplitude of the slow component decreased with a time lag of about 2 min when external Na(+) was reduced. A previous exposure of the retina to a Na(+)-free Ringer solution for at least 3 min modified the voltage photoresponse in a way similar to that observed in the presence of 100 muM-strophanthidin.8. When external Ca(2+) concentration (Ca(2+)) was increased from 2 to 5 mM the slow component decreased by about 30%. When Ca(2+) was reduced the slow component increased. A twofold increase was observed when Ca(2+) was lower than 10(-4) M.9. It is suggested that the slow component of the voltage response in the presence of external Cs(+) is caused by an electrogenic current driven by the Na(+)-K(+) transport system, during a voltage-dependent block of external Cs(+) of some K(+) channels.
摘要
  1. 在改变细胞外液离子成分的同时,记录分离的蟾蜍视网膜中视杆细胞的膜电位。

  2. 浓度为1 mM的铯(Cs(+))足以完全阻断明闪光电压响应中从峰值到平台期的下垂。

  3. 在存在10 mM - Cs(+)的情况下,明闪光响应的幅度增加到约90 mV,从而达到 - 110至 - 135 mV之间的绝对膜电位。这些响应包括一个约35 mV的初始快速成分,随后是一个慢得多的成分,其幅度可达50 mV。

  4. 在初始快速成分的峰值处,视杆细胞膜的行为与P(Na)/P(K)比为0.023的钾电极非常相似。在存在2.6 mM - K(+)的情况下,慢成分的平均幅度约为35 mV,而在无钾林格液中则降至约25 mV。

  5. 向灌流液中添加100 μM毒毛花苷会引起视杆细胞电活动的几种可逆变化。暗静息膜电位去极化约5 mV,对暗光闪烁的电压响应动力学减慢。电压敏感性最初增加约30%,但对明闪光的响应峰值降低约13 mV。

  6. 在经10 mM - Cs(+)处理的视杆细胞中,毒毛花苷以3 μM的表观米氏常数消除了明闪光响应中存在的慢成分。

  7. 当外部钠离子(Na(+))减少时,慢成分的幅度会有大约2分钟的延迟下降。视网膜先前暴露于无钠林格液中至少3分钟,对视杆细胞电压光响应的改变方式与在存在100 μM毒毛花苷时观察到的相似。

  8. 当外部钙离子浓度(Ca(2+))从2 mM增加到5 mM时,慢成分减少约30%。当Ca(2+)降低时,慢成分增加。当Ca(2+)低于10(-4) M时,观察到慢成分增加了两倍。

  9. 有人认为,在外部存在Cs(+)的情况下,电压响应的慢成分是由钠钾转运系统驱动的生电电流引起的,此时外部Cs(+)对一些钾通道产生电压依赖性阻断。

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