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从大鼠浅表背角的神经胶质细胞记录到的缓慢去极化电位。

Slow depolarizing potentials recorded from glial cells in the rat superficial dorsal horn.

作者信息

Takahashi T, Tsuruhara H

机构信息

Department of Physiology, Kyoto University, Faculty of Medicine, Japan.

出版信息

J Physiol. 1987 Jul;388:597-610. doi: 10.1113/jphysiol.1987.sp016633.

Abstract
  1. Intracellular potentials were recorded from inexcitable cells in the superficial dorsal horn of the rat lumbar spinal cord in vitro. 2. These cells had a large resting membrane potential (up to -90 mV) but when depolarized were unable to produce action potentials. The resting potential was highly dependent upon extracellular K+ concentrations ([K+]o), with a slope of about 45 mV for a 10-fold change in [K+]o. 3. Electrical stimulation of dorsal roots evoked a slow depolarizing potential lasting for many seconds in the inexcitable cells. The slow potentials were not accompanied by any appreciable change in input conductance, nor were their amplitudes dependent upon the membrane potential. 4. The morphology of the inexcitable cells marked by intracellular injection of a fluorescent dye, Lucifer Yellow, was consistent with their being glial cells. 5. [K+]o values were measured by K+-sensitive electrodes simultaneously with intracellular glial potentials. Changes in the K+-electrode potential occurred in parallel with slow depolarizing potentials following stimulation of dorsal roots. When the stimulus intensity was altered, changes in the magnitude of the K+-electrode response were correlated with those of the slow potentials. 6. Replacement of extracellular Ca2+ by Mg2+ abolished both the slow potentials and K+-electrode responses evoked by afferent stimulation, suggesting that impulses in primary afferent fibres do not directly contribute to the glial slow potentials. 7. It is concluded that the slow potentials in glial cells result from a transient increase in [K+]o at the superficial dorsal horn, which is induced by activation of neighbouring internuncial neurones.
摘要
  1. 在体外对大鼠腰段脊髓背角浅层的非兴奋性细胞记录细胞内电位。2. 这些细胞具有较大的静息膜电位(高达 -90 mV),但去极化时无法产生动作电位。静息电位高度依赖于细胞外钾离子浓度([K+]o),[K+]o 变化 10 倍时斜率约为 45 mV。3. 电刺激背根在非兴奋性细胞中诱发持续数秒的缓慢去极化电位。缓慢电位不伴有输入电导的任何明显变化,其幅度也不依赖于膜电位。4. 通过细胞内注射荧光染料鲁米诺黄标记的非兴奋性细胞的形态与它们是神经胶质细胞一致。5. 用钾离子敏感电极同时测量 [K+]o 值和神经胶质细胞内电位。刺激背根后,钾离子电极电位的变化与缓慢去极化电位平行发生。当刺激强度改变时,钾离子电极反应幅度的变化与缓慢电位的变化相关。6. 用镁离子取代细胞外钙离子消除了传入刺激诱发的缓慢电位和钾离子电极反应,表明初级传入纤维中的冲动不直接导致神经胶质细胞的缓慢电位。7. 得出结论,神经胶质细胞中的缓慢电位是由背角浅层 [K+]o 的短暂升高引起的,这是由相邻中间神经元的激活诱导的。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f794/1192567/e62a4de238b7/jphysiol00529-0590-a.jpg

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