Müller W, Misgeld U, Heinemann U
Abteilung Neurophysiologie, Max-Planck-Institut für Psychiatrie, Planegg-Martinsried, Federal Republic of Germany.
Exp Brain Res. 1988;72(2):287-98. doi: 10.1007/BF00250251.
Nominally K-sensitive microelectrodes were used to measure carbachol (CCh) in order to study the dependence of muscarinic effects on CCh concentration and exposure time in guinea pig hippocampal slices. Interference presumably originating from tissue choline-compounds was neutralized by pre-equilibration of the slices with 500 microM choline and calibration of the CCh-sensitive microelectrodes in the presence of the same choline-concentration. Muscarinic depolarization and reduction of the afterhyperpolarization (AHP) following a train of action potentials by bath applied CCh were monitored in granule cells and CA3 pyramidal neurons by intracellular recording. A fast bath application mode of CCh was designed, by which CCh tissue concentration reached a peak after 2-3 min and was washed out with a half time of about 8 min. After application of 30 nmol CCh in this way, the AHP was reduced according to the variation of CCh concentration over time. Neurons depolarized with some delay after the reduction of the AHP and started to repolarize 1 min before the peak of tissue CCh concentration (0.6 microM) was reached. Pirenzepine (1-10 microM) blocked only the depolarization, while atropine (1-10 microM) blocked both the depolarization and the reduction of the AHP. When superfusing with CCh containing saline, 80% of the final concentration was reached in the bath after 12 min, but in the tissue only after 45 min. The slow increase of tissue CCh concentration was concurrent with the slow decrease of the AHP. No effect on the membrane potential was observed. Atropine, but not pirenzepine, blocked the reduction of the AHP. Superfusion with a high CCh concentration (100-300 microM) containing saline depolarized neurons and reduced the AHP. Then pirenzepine repolarized neurons, whereas atropine both repolarized the cells and restored the AHP. It is concluded tha the muscarinic depolarization depends not only on the CCh concentration, but also on the rate of rise of CCh, while the reduction of the AHP depends solely on the concentration. This result is discussed in terms of the possibility that the depolarization is mediated by a short term desensitizing M1 muscarinic receptor subtype and the reduction of the AHP is mediated by a M2 muscarinic receptor subtype.
为了研究豚鼠海马切片中,毒蕈碱样效应与卡巴胆碱(CCh)浓度和暴露时间的关系,使用了名义上对钾离子敏感的微电极来测量CCh。通过用500微摩尔胆碱对切片进行预平衡,并在相同胆碱浓度存在的情况下对CCh敏感微电极进行校准,来中和可能源于组织胆碱化合物的干扰。通过细胞内记录,监测颗粒细胞和CA3锥体神经元中,浴加CCh后毒蕈碱样去极化以及一串动作电位后超极化(AHP)的降低情况。设计了一种快速浴加CCh的模式,通过这种模式,CCh组织浓度在2 - 3分钟后达到峰值,并以约8分钟的半衰期被洗脱。以这种方式施加30纳摩尔CCh后,AHP根据CCh浓度随时间的变化而降低。AHP降低后,神经元有一定延迟地去极化,并在组织CCh浓度峰值(0.6微摩尔)达到前1分钟开始复极化。哌仑西平(1 - 10微摩尔)仅阻断去极化,而阿托品(1 - 10微摩尔)同时阻断去极化和AHP的降低。当用含CCh的生理盐水灌注时,12分钟后浴中达到最终浓度的80%,但组织中仅在45分钟后达到。组织CCh浓度的缓慢升高与AHP的缓慢降低同时发生。未观察到对膜电位的影响。阿托品而非哌仑西平阻断了AHP的降低。用含高浓度CCh(100 - 300微摩尔)的生理盐水灌注使神经元去极化并降低了AHP。然后哌仑西平使神经元复极化,而阿托品既使细胞复极化又恢复了AHP。得出的结论是,毒蕈碱样去极化不仅取决于CCh浓度,还取决于CCh的上升速率,而AHP的降低仅取决于浓度。根据去极化由短期脱敏的M1毒蕈碱受体亚型介导以及AHP的降低由M2毒蕈碱受体亚型介导的可能性,对这一结果进行了讨论。