Backus K H, Berger T, Kettenmann H
Department of Neurobiology, University of Heidelberg, F.R.G.
Brain Res. 1991 Feb 8;541(1):103-9. doi: 10.1016/0006-8993(91)91081-b.
Short application of the neurokinin receptor agonist substance P (SP) leads to a biphasic depolarization of astrocytes cultured from rat cortex. The rapid and transient depolarizing event lasted few seconds, the slow one several minutes. In some cells, only the slow depolarizing component was observed. During the slow depolarizing event, the sensitivity of the membrane potential for a change in the K+ gradient decreased, indicating a decrease in the relative K+ permeability of the membrane. The rapid SP-induced depolarization could be reversed, when the membrane potential was depolarized to about 0 mV by elevation of the extracellular K+ concentration, indicating a reversal potential close to the Cl- equilibrium potential. When the membrane was clamped close to the resting membrane potential using the whole-cell patch-clamp technique, SP induced a biphasic inward current with a similar time course as the SP-induced membrane depolarization. Evaluating current-to-voltage curves indicated a conductance decrease during the slow inward current with a reversal potential of the SP-dependent current close to the K+ equilibrium potential. The mean open time of single K+ channels, measured in the cell-attached configuration of the patch-clamp technique, decreased after application of SP. In contrast, the mean open time of single Cl- channels increased. We conclude that activation of neurokinin receptors in astrocytes modulates the activity of K+ and Cl- channels, leading to a complex depolarization of the membrane potential.
短暂应用神经激肽受体激动剂P物质(SP)会导致从大鼠皮层培养的星形胶质细胞出现双相去极化。快速且短暂的去极化事件持续几秒,缓慢的去极化事件持续几分钟。在一些细胞中,仅观察到缓慢的去极化成分。在缓慢去极化事件期间,膜电位对K⁺梯度变化的敏感性降低,表明膜的相对K⁺通透性降低。当通过提高细胞外K⁺浓度使膜电位去极化至约0 mV时,SP诱导的快速去极化可以被逆转,这表明逆转电位接近Cl⁻平衡电位。当使用全细胞膜片钳技术将膜钳制在接近静息膜电位时,SP诱导出双相内向电流,其时间进程与SP诱导的膜去极化相似。评估电流 - 电压曲线表明,在缓慢内向电流期间电导降低,且SP依赖性电流的逆转电位接近K⁺平衡电位。在膜片钳技术的细胞贴附模式下测量的单个K⁺通道的平均开放时间在应用SP后减少。相反,单个Cl⁻通道的平均开放时间增加。我们得出结论,星形胶质细胞中神经激肽受体的激活调节K⁺和Cl⁻通道的活性,导致膜电位出现复杂的去极化。