Barbour B, Keller B U, Llano I, Marty A
Laboratoire de Neurobiologie, Ecole Normale Supérieure, Paris, France.
Neuron. 1994 Jun;12(6):1331-43. doi: 10.1016/0896-6273(94)90448-0.
In the molecular layer of the cerebellar cortex, Purkinje cells and interneurons receive a common excitatory input from parallel fibers. The AMPA/kainate receptor-mediated parallel fiber excitatory postsynaptic current (EPSC) recorded in Purkinje cells decays much more slowly than that recorded in interneurons. We show that this slowness of decay does not result from dendritic filtering and that it is unlikely to reflect the deactivation kinetics of the postsynaptic receptors. Agents blocking glutamate uptake prolong the EPSC in Purkinje cells. We conclude that the slow EPSC decay results from the continued presence of transmitter glutamate. This may be due to retarded transmitter diffusion around spines or to cross-talk between neighboring active synapses.
在小脑皮质的分子层中,浦肯野细胞和中间神经元从平行纤维接收共同的兴奋性输入。在浦肯野细胞中记录到的由AMPA/海人藻酸受体介导的平行纤维兴奋性突触后电流(EPSC)的衰减比在中间神经元中记录到的要慢得多。我们表明,这种衰减的缓慢并非源于树突滤波,也不太可能反映突触后受体的失活动力学。阻断谷氨酸摄取的药物会延长浦肯野细胞中的EPSC。我们得出结论,EPSC衰减缓慢是由于递质谷氨酸持续存在。这可能是由于递质在棘突周围扩散受阻,或者是相邻活跃突触之间的串扰所致。