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对蝾螈视网膜单个视杆细胞内节中的电压激活电流和钙激活电流进行了研究。

Voltage-activated and calcium-activated currents studied in solitary rod inner segments from the salamander retina.

作者信息

Bader C R, Bertrand D, Schwartz E A

出版信息

J Physiol. 1982 Oct;331:253-84. doi: 10.1113/jphysiol.1982.sp014372.

DOI:10.1113/jphysiol.1982.sp014372
PMID:7153904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1197749/
Abstract
  1. Solitary rod inner segments were obtained by enzymatic dissociation of the tiger salamander (Ambystoma tigrinum) retina. Their membrane currents were studied with the single-pipette voltage-clamp technique. Individual currents were isolated with the aid of pharmacological agents.2. Extracellular caesium blocked a current activated by hyperpolarization from -30 mV. Changing external sodium and potassium concentrations altered the value of the reversal potential in a manner consistent with the current being carried equally by both ions.3. Extracellular tetraethylammonium (TEA) blocked a current activated by depolarization from -70 mV. In normal medium this current had a reversal potential of -72 mV. Changing the external potassium concentration altered the value of the reversal potential in a manner consistent with the current being carried predominantly by potassium.4. Extracellular cobalt blocked a current activated by depolarization that had an initial inward and a later outward component.5. After EGTA was injected into an inner segment the outward component was suppressed. Cobalt then blocked an inward current. This current is believed to be carried predominantly by calcium. The conductance increased with depolarization from -45 mV and reached a maximum at approximately 0 mV. Following a step of depolarization the current activated rapidly (< 20 msec) and then remained constant for at least several seconds without evidence of inactivation.6. Injecting caesium into an inner segment eliminated a calcium-activated outward current believed to be carried by potassium ions.7. After the injection of caesium there remained another calcium-activated current with a reversal potential of -17 mV. Changing extracellular chloride concentration altered the value of the reversal potential in a manner consistent with chloride carrying at least 70% of the current. Another anion may carry the balance.8. When the five currents mentioned in items 2, 3, 5, 6 and 7 were blocked, the membrane resistance between -90 and -25 mV was linear, time-independent, and had a high value (2.1 GOmega).9. The five identified currents can all be activated in the physiological range of voltage in which salamander rods normally operate.
摘要
  1. 通过酶解虎螈(Ambystoma tigrinum)视网膜获得单个视杆细胞内段。采用单吸管电压钳技术研究其膜电流。借助药理试剂分离出单个电流。

  2. 细胞外铯阻断了从 -30 mV 超极化激活的电流。改变细胞外钠和钾浓度,以与两种离子等量携带电流相一致的方式改变了反转电位的值。

  3. 细胞外四乙铵(TEA)阻断了从 -70 mV 去极化激活的电流。在正常培养基中,该电流的反转电位为 -72 mV。改变细胞外钾浓度,以与电流主要由钾携带相一致的方式改变了反转电位的值。

  4. 细胞外钴阻断了由去极化激活的电流,该电流最初为内向电流,随后为外向电流。

  5. 将乙二醇双四乙酸(EGTA)注入内段后,外向电流成分受到抑制。然后钴阻断了内向电流。据信该电流主要由钙携带。电导从 -45 mV 去极化时增加,并在约 0 mV 达到最大值。在去极化步骤后,电流迅速激活(<20 毫秒),然后至少持续数秒保持恒定,无失活迹象。

  6. 将铯注入内段消除了一种据信由钾离子携带的钙激活外向电流。

  7. 注入铯后,仍存在另一种钙激活电流,其反转电位为 -17 mV。改变细胞外氯浓度,以与氯至少携带 70% 的电流相一致的方式改变了反转电位的值。另一种阴离子可能携带其余部分。

  8. 当第 2、3、5、6 和 7 项中提到的五种电流被阻断时,-90 至 -25 mV 之间的膜电阻呈线性、与时间无关,且具有高值(2.1 GΩ)。

  9. 所确定的这五种电流都可在虎螈视杆细胞正常运作的生理电压范围内被激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/1197749/a33abfa95476/jphysiol00671-0297-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/1197749/a33abfa95476/jphysiol00671-0297-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/1197749/a33abfa95476/jphysiol00671-0297-a.jpg

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