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金鱼延髓中的电介导抑制。

An electrically mediated inhibition in goldfish medulla.

作者信息

Korn H, Faber D S

出版信息

J Neurophysiol. 1975 Mar;38(2):452-71. doi: 10.1152/jn.1975.38.2.452.

Abstract
  1. Passive hyperpolarizing potentials (PHPs) have been recorded intracellularly from goldfish medullary neurons in the vicinity of the Mauthner cell (M-cell). They are evoked when this cell is activated antidromically by stimulation of the spinal cord, and orthodromically via the ipsilateral eighth nerve; when appropriately timed they block or delay spikes induced both directly and transsynaptically. 2. Since the PHPs and the M-cell spike have the same latency, time course, and all-or-none character, they cannot be generated by chemically mediated synaptic transmission. This conclusion is further supported by the evidence that PHP amplitude and time course are independent of membrane potential. 3. The analysis of the mechanism underlying PHP generation has been based on the hypothesis that they are brought about by the extracellular currents flowing to the axon cap during an M-cell action potential. Specifically, it was postulated that some of this current is channeled back to the axon cap region intracellularly through processes of PHP-exhibiting neurons, and that these cells are passively hyperpolarized by the associated inward transmembrane current flow. This model would require that PHP-exhibiting neurons send processes into the axon cap. This hypothesis is confirmed by the following: a) When the PHP is timed to occur during the conductance increase associated with a spike after hyperpolarization, it is reduced, as would be expected for a passive current flow across a membrane resistance. b) PHPs are not found in all medullary neurons in the vicinity of the M-cell, but rather in a specific neuronal population. c) PHP-exhibiting neurons have been identified following Procion yellow injections; as predicted, they issue one process, presumably the axon, which projects toward the M-cell axon cap area. d) The PHP can be stimulated by passing a cathodal current from a microelectrode located in the axon cap; it is not mimicked when the cathodal electrode is moved outside this region. The currents necessary to mimic a PHP are comparable to the estimated current flowing back to the axon cap during an M-cell action potential. 4. The input resistance of PHP-exhibiting neurons is in the range of 4 M alpha, and their estimated specific membrane resistance is in the range of 900-2,000 alpha-cm-2, which is not an unusually low value for neuronal membranes. By contrast, the intracellular channeling of current during a PHP can rather be attributed to a high extracellular tissue resistance within the axon cap, which was found to be at least 2.5 times that of the surrounding medullary tissue..
摘要
  1. 被动超极化电位(PHPs)已在金鱼延髓中与莫纳细胞(M细胞)相邻区域的神经元内记录到。当通过刺激脊髓对该细胞进行逆向激活,或通过同侧第八对脑神经进行顺向激活时,它们就会被诱发;当时间安排适当时,它们会阻断或延迟直接和经突触诱导的动作电位。2. 由于PHPs和M细胞动作电位具有相同的潜伏期、时程和全或无特性,它们不可能由化学介导的突触传递产生。PHP幅度和时程与膜电位无关这一证据进一步支持了这一结论。3. 对PHP产生机制的分析基于这样一种假设,即它们是由M细胞动作电位期间流向轴突帽的细胞外电流引起的。具体而言,推测部分这种电流通过表现出PHP的神经元的突起在细胞内回流到轴突帽区域,并且这些细胞因相关的内向跨膜电流而被被动超极化。该模型要求表现出PHP的神经元将突起发送到轴突帽。以下内容证实了这一假设:a)当PHP被安排在超极化后与动作电位相关的电导增加期间出现时,它会减小,这正如跨膜电阻上被动电流流动所预期的那样。b)并非在M细胞附近的所有延髓神经元中都能发现PHPs,而是在特定的神经元群体中发现。c)在注射普施安黄后已鉴定出表现出PHP的神经元;正如所预测的,它们发出一个突起,大概是轴突,其朝向M细胞轴突帽区域投射。d)可以通过从位于轴突帽中的微电极通阴极电流来刺激PHP;当阴极电极移到该区域之外时则不会模拟出PHP。模拟PHP所需的电流与M细胞动作电位期间估计回流到轴突帽的电流相当。4. 表现出PHP的神经元的输入电阻在4 MΩ范围内,其估计的比膜电阻在900 - 2000 Ω·cm²范围内,这对于神经元膜来说并不是异常低的值。相比之下,PHP期间电流的细胞内引导更可归因于轴突帽内高的细胞外组织电阻,已发现其至少是周围延髓组织电阻的2.5倍。

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