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大鼠脊髓背角神经元中的低电压和高电压激活钙电流

Low- and high-voltage-activated calcium currents in rat spinal dorsal horn neurons.

作者信息

Ryu P D, Randic M

机构信息

Department of Veterinary Physiology and Pharmacology, Iowa State University, Ames 50011.

出版信息

J Neurophysiol. 1990 Feb;63(2):273-85. doi: 10.1152/jn.1990.63.2.273.

Abstract
  1. Calcium currents in immature rat spinal dorsal horn neurons in transverse slices were studied with the single-electrode voltage-clamp technique. Using experimental conditions that minimized voltage-dependent Na+ and K+ currents, we distinguished low- and high-voltage-activated calcium currents on the basis of their voltage dependence and sensitivity to the Ca2(+)-channel agonist and antagonist drugs. 2. The low-voltage-activated transient calcium current is evoked with weak depolarizing voltage commands. It begins to activate at potentials positive to -70 mV and increases in amplitude and rate of decay with depolarization, the peak values being reached between -40 and -30 mV. The current is fully activated at a holding potential of about -110 mV. Steady-state inactivation is complete at potentials in the range of -60 to -50 mV. 3. The transient component of the high-threshold calcium current appears at membrane potentials close to -40 mV and slowly decays within several hundreds of milliseconds. The amplitude of the current increases with more negative holding potentials (-100 to -40 mV). 4. The sustained component of the high-threshold calcium current seems to activate at potentials positive to -40 mV and exhibits little inactivation during 0.3- to 0.5-s depolarizing commands. This component is better isolated at more depolarized holding potentials (between -40 and -30 mV) that inactivate the transient components of the low- and high-threshold calcium currents. 5. A rundown of calcium currents was seen in dorsal horn cells. The time stability of the transient and sustained components of the high-threshold calcium current was lower than that of the low-threshold transient current. The latter current seemed to be insensitive up to 1 h. 6. (-)-Bay K 8644 (1-10 microM), a dihydropyridine agonist, enhanced the high-threshold calcium current, in particular the sustained component, but not the transient low-threshold calcium current. The dihydropyridine antagonist nifedipine (5-50 microM) selectively reduced the sustained component of the high-threshold calcium current while having little or no effect on the transient components of the low- and high-threshold calcium currents. 7. Cadmium ions (60-100 microM) and cobalt ions (2 mM) markedly reduced both components of the high-threshold calcium current, and Cd2+ only slightly decreased the low-threshold transient current. However, all three components are indiscriminately blocked by higher concentrations of Cd2+ and Co2+.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用单电极电压钳技术研究了未成熟大鼠脊髓背角神经元横切片中的钙电流。利用使电压依赖性钠电流和钾电流最小化的实验条件,我们根据其电压依赖性以及对钙通道激动剂和拮抗剂药物的敏感性,区分了低电压激活和高电压激活的钙电流。2. 低电压激活的瞬时钙电流由微弱的去极化电压指令诱发。它在正于 -70 mV 的电位开始激活,随着去极化其幅度和衰减速率增加,峰值在 -40 至 -30 mV 之间达到。该电流在约 -110 mV 的钳制电位下完全激活。稳态失活在 -60 至 -50 mV 的电位范围内完成。3. 高阈值钙电流的瞬时成分出现在接近 -40 mV 的膜电位处,并在几百毫秒内缓慢衰减。电流幅度随着更负的钳制电位(-100 至 -40 mV)增加。4. 高阈值钙电流的持续成分似乎在正于 -40 mV 的电位激活,并且在 0.3 至 0.5 秒的去极化指令期间几乎没有失活。该成分在更去极化的钳制电位(-40 至 -30 mV 之间)能更好地分离出来,此电位会使低阈值和高阈值钙电流的瞬时成分失活。5. 在背角细胞中观察到钙电流的衰减。高阈值钙电流的瞬时和持续成分的时间稳定性低于低阈值瞬时电流。后者的电流在长达一小时内似乎不敏感。6. 二氢吡啶激动剂(-)-Bay K 8644(1 - 10 μM)增强了高阈值钙电流,特别是持续成分,但不增强低阈值瞬时钙电流。二氢吡啶拮抗剂硝苯地平(5 - 50 μM)选择性地降低了高阈值钙电流的持续成分,而对低阈值和高阈值钙电流的瞬时成分几乎没有影响或没有影响。7. 镉离子(60 - 100 μM)和钴离子(2 mM)显著降低了高阈值钙电流的两个成分,并且 Cd2 + 仅轻微降低了低阈值瞬时电流。然而,更高浓度的 Cd2 + 和 Co2 + 会无差别地阻断所有三个成分。(摘要截于 400 字)

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