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从金鱼视网膜分离出的单个水平细胞的膜特性。

Membrane properties of solitary horizontal cells isolated from goldfish retina.

作者信息

Tachibana M

出版信息

J Physiol. 1981 Dec;321:141-61. doi: 10.1113/jphysiol.1981.sp013976.

Abstract
  1. Solitary horizontal cells were obtained by dissociating the adult goldfish retina using the enzyme papain. The cells were identified on morphological grounds and could be kept in culture for over a week. 2. Solitary horizontal cells, penetrated with micro-electrodes, had resting potentials of about -75 mV in normal solution. When external K+ concentration was changed, the membrane potential varied from EK calculated from the Nernst equation. 3. All solitary horizontal cells tested showed an action potential in response to superthreshold depolarizing current pulses. The action potential had an overshoot of about +20 mV and a plateau potential lasting for several seconds. 4. The action potential appeared to be Ca-dependent for the following reasons: (a) TTX or low [Na+] did not affect the action potential, (b) Sr2+, Ba2+ or high [Ca2+] enhanced the action potential, while (c) Co2+ or high [Mg2+] blocked it. No regenerative activity has been observed in horizontal cells in the retina but it is possible that the regenerative mechanism is suppressed normally. 5. A role for K+ was indicated by an increase in the duration and amplitude of the action potential on the application of tetraethylammonium. 6. The steady-state current--voltage (I--V) curve, measured by applying constant current pulses, was S-shaped (current on the abscissa) and composed of inward- and outward-going rectifying regions and a transitional region between them. A similar non-linear I--V relationship has been reported in vivo. 7. The transitional region was characterized by a sudden potential jump and hysteresis, suggesting the presence of a 'negative resistance'. This potential jump appeared not to be produced by the Ca-conductance mechanism mentioned above, since similar jumps were observed in the presence of Co2+.
摘要
  1. 通过用木瓜蛋白酶解离成年金鱼视网膜获得孤立的水平细胞。这些细胞根据形态学特征得以识别,并且能够在培养中保存超过一周。2. 用微电极刺入的孤立水平细胞在正常溶液中的静息电位约为 -75 mV。当外部钾离子浓度改变时,膜电位根据能斯特方程计算得出的 EK 而变化。3. 所有测试的孤立水平细胞对阈上去极化电流脉冲均表现出动作电位。该动作电位有大约 +20 mV 的超射值和持续数秒的平台电位。4. 动作电位似乎依赖于钙离子,原因如下:(a) 河豚毒素或低 [钠离子] 不影响动作电位,(b) 锶离子、钡离子或高 [钙离子] 增强动作电位,而 (c) 钴离子或高 [镁离子] 阻断动作电位。在视网膜的水平细胞中未观察到再生活动,但正常情况下再生机制有可能受到抑制。5. 应用四乙铵后动作电位的持续时间和幅度增加,表明钾离子起作用。6. 通过施加恒定电流脉冲测量的稳态电流 - 电压 (I - V) 曲线呈 S 形(横坐标为电流),由内向和外向整流区域以及它们之间的过渡区域组成。体内也报道过类似的非线性 I - V 关系。7. 过渡区域的特征是电位突然跳跃和滞后现象,表明存在“负电阻”。这种电位跳跃似乎不是由上述钙离子电导机制产生的,因为在存在钴离子的情况下也观察到了类似的跳跃。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcff/1249618/94ee9d67526c/jphysiol00728-0148-a.jpg

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