Abteilung für Allgemeine Zoologie, FB Biologie, Universität Kaiserslautern, Postfach 3049, D-67653 Kaiserslautern, Germany.
Pflugers Arch. 1998 Jul;436(4):608-14. doi: 10.1007/s004240050678.
We have measured membrane current, membrane potential and intracellular Na+ and Ca2+ concentrations, [Na+]i and [Ca2+]i, of the giant glial cell in the nervous system of the leech Hirudo medicinalis using conventional microelectrodes and the fluorescent dyes sodium-binding benzofuran isophthalate (SBFI) and fura-2. When the Na+ was removed from the saline, the membrane conductance increased twofold from 1.29±0.1 µS to 2.57±0.18 µS (mean ± SEM; n=27). The rise in membrane conductance was accompanied by a current, which reversed around –74 mV, and the amplitude of K+-induced depolarizations or currents increased during Na+ removal, suggesting an increase in the K+ conductance of the glial membrane. We also monitored [Ca2+]i when removing external Na+ in the presence and absence of external Ca2+, and during injection of the Ca2+-chelator BAPTA into the cells. Our results indicate that Na+ modulates a K+ conductance of these glial cells, independent of intra- and extracellular Ca2+.
我们使用常规微电极和荧光染料钠离子结合苯并呋喃异邻苯二甲酸盐(SBFI)和 fura-2 测量了医用水蛭神经系统中巨大神经胶质细胞的膜电流、膜电位以及细胞内 Na+和 Ca2+浓度 [Na+]i 和 [Ca2+]i。当将 Na+从盐水中去除时,膜电导从 1.29±0.1 µS 增加到 2.57±0.18 µS(平均值 ± SEM;n=27)。膜电导的增加伴随着电流的出现,该电流在约-74 mV 处反转,并且在 Na+去除期间,K+-诱导的去极化或电流的幅度增加,这表明神经胶质细胞膜的 K+电导增加。当在存在和不存在外 Ca2+的情况下去除外 Na+时,以及在将 Ca2+螯合剂 BAPTA 注入细胞时,我们还监测了 [Ca2+]i。我们的结果表明,Na+调节这些神经胶质细胞的 K+电导,而与细胞内外 Ca2+无关。