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猫新皮层神经元中钠依赖性钾电流对兴奋性的长期降低作用。

Long-lasting reduction of excitability by a sodium-dependent potassium current in cat neocortical neurons.

作者信息

Schwindt P C, Spain W J, Crill W E

机构信息

Department of Physiology and Biophysics, University of Washington School of Medicine, Seattle 98195.

出版信息

J Neurophysiol. 1989 Feb;61(2):233-44. doi: 10.1152/jn.1989.61.2.233.

Abstract
  1. The function and ionic mechanism of a slow outward current were studied in large layer V neurons of cat sensorimotor cortex using an in vitro slice preparation and single microelectrode voltage clamp. 2. With Ca2+ influx blocked, a slow relaxation ("tail") of outward current followed either (1) repetitive firing evoked for 1 s or (2) a small 1-s depolarizing voltage clamp step that activated the persistent Na+ current of neocortical neurons, INaP. When a depolarization that activated INaP was maintained, an outward current gradually developed and increased in amplitude over a period of tens of seconds to several minutes. An outward tail current of similar duration followed repolarization. The slow outward current was abolished by TTX, indicating it depended on Na+ influx. 3. With Ca2+ influx blocked, the onset of the slow Na+-dependent outward current caused spike frequency adaptation during current-evoked repetitive firing. Following the firing, the decay of the Na+-dependent current caused a slow afterhyperpolarization (sAHP) and a long-lasting reduction of excitability. It also was responsible for habituation of the response to repeated identical current pulses. 4. The Na+-dependent tail current had properties expected of a K+ current. Membrane chord conductance increased during the tail, and tail amplitude was reduced or reversed by membrane potential hyperpolarization and raised extracellular K+ concentration [( K+]0). 5. The current tail was reduced reversibly by the K+ channel blockers TEA (5-10 mM), muscarine (5-20 microM), and norepinephrine (100 microM). These agents also resulted in a larger, more sustained inward current during the preceding step depolarization. Comparison of current time course before and after the application of blocking agents suggested that, in spite of its capability for slow buildup and decay, the onset of the Na+-dependent outward current occurs within 100 ms of an adequate step depolarization. 6. With Ca2+ influx blocked, extracellular application of dantrolene sodium (30 microM) had no clear effect on the current tail or the corresponding sAHP.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 利用体外脑片制备技术和单微电极电压钳,研究了猫感觉运动皮层V层大神经元中缓慢外向电流的功能和离子机制。2. 在Ca2+内流被阻断的情况下,外向电流的缓慢松弛(“尾电流”)出现在以下两种情况之后:(1)持续1秒的重复放电;(2)一个持续1秒的小去极化电压钳步骤,该步骤激活了新皮层神经元的持续性钠电流(INaP)。当维持激活INaP的去极化时,外向电流逐渐形成,并且在几十秒到几分钟的时间内幅度增大。复极化后会出现持续时间相似的外向尾电流。缓慢外向电流被TTX消除,表明它依赖于Na+内流。3. 在Ca2+内流被阻断的情况下,依赖于Na+的缓慢外向电流的起始导致了电流诱发重复放电期间的放电频率适应。放电之后,依赖于Na+的电流的衰减导致了缓慢的超极化后电位(sAHP)和兴奋性的长期降低。它还导致了对重复相同电流脉冲反应的习惯化。4. 依赖于Na+的尾电流具有钾电流所预期的特性。尾电流期间膜弦电导增加,并且尾电流幅度通过膜电位超极化和细胞外钾离子浓度升高([K+]0)而降低或反转。5. 钾通道阻滞剂TEA(5 - 10 mM)、毒蕈碱(5 - 20 microM)和去甲肾上腺素(100 microM)可使电流尾电流可逆性降低。这些药物还导致在前一步去极化期间出现更大、更持久的内向电流。比较应用阻断剂前后的电流时间进程表明,尽管依赖于Na+的外向电流具有缓慢形成和衰减的能力,但其起始发生在适当的阶跃去极化的100毫秒内。6. 在Ca2+内流被阻断的情况下,细胞外应用丹曲林钠(30 microM)对电流尾电流或相应的sAHP没有明显影响。(摘要截短至400字)

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