Jouvenceau A, Billard J M, Wiley R G, Lamour Y, Dutar P
Laboratoire de Physiopharmacologie du Système Nerveux, INSERM U 161, Paris, France.
Neuroreport. 1994 Sep 8;5(14):1781-4. doi: 10.1097/00001756-199409080-00024.
The consequences of intracerebroventricular injection of the toxin 192-IgG-saporin on the electrophysiological properties of CA1 pyramidal cells were investigated using intracellular recordings in the in vitro hippocampal slice preparation. We present the first electrophysiological evidence of a dysfunction of hippocampal cholinergic afferents following injection of 192-IgG-saporin. The synaptic events mediated by acetylcholine were altered in such animals: the slow cholinergic excitatory postsynaptic potentials as well as the cholinergic activation of GABAergic interneurones were dramatically depressed or even absent; the amplitude and duration of the afterhyperpolarization following a burst of spikes were increased, while other neuronal properties were not modified. These specific alterations suggest that the toxin 192-IgG-saporin is a specific tool for the experimental study of cholinergic denervation in the hippocampus.
采用体外海马脑片制备技术,通过细胞内记录,研究了脑室内注射毒素192-IgG-皂草素对CA1锥体细胞电生理特性的影响。我们首次提供了注射192-IgG-皂草素后海马胆碱能传入神经功能障碍的电生理证据。在这些动物中,由乙酰胆碱介导的突触事件发生了改变:缓慢的胆碱能兴奋性突触后电位以及GABA能中间神经元的胆碱能激活显著降低甚至消失;一串动作电位后的超极化后电位的幅度和持续时间增加,而其他神经元特性未改变。这些特异性改变表明,毒素192-IgG-皂草素是海马胆碱能去神经支配实验研究的一种特异性工具。