Ajima A, Hensch T, Kado R T, Ito M
Laboratory for Neural Networks, Frontier Research Program, RIKEN, Saitama, Japan.
Neurosci Res. 1991 Oct;12(1):281-6. doi: 10.1016/0168-0102(91)90117-h.
Synaptic potentials were recorded intracellularly from Purkinje cells in guinea pig cerebellar slices. EPSPs evoked by stimulation of parallel fibers were effectively blocked by perfusion of a slice with the synthetic analog of Joro spider toxin, 1-naphthylacetyl-spermine (NAS) at 250 microM. However, it did not influence those responses evoked by stimulation of climbing fibers. This action of NAS is in contrast to other commonly used glutamate antagonists, CNQX or APV: CNQX (5 microM) blocked both parallel fiber- and climbing fiber-induced responses, while APV (up to 1 mM) did not influence either except for a weak reduction observed in climbing fiber responses. NAS thus provides a useful tool for pharmacologically distinguishing parallel fiber and climbing fiber synapses.
在豚鼠小脑切片中,从浦肯野细胞内记录突触电位。用250微摩尔的Joro蜘蛛毒素合成类似物1-萘乙酰精胺(NAS)灌注切片,可有效阻断平行纤维刺激诱发的兴奋性突触后电位(EPSP)。然而,它并不影响攀缘纤维刺激诱发的反应。NAS的这种作用与其他常用的谷氨酸拮抗剂CNQX或APV不同:CNQX(5微摩尔)可阻断平行纤维和攀缘纤维诱发的反应,而APV(高达1毫摩尔)除了对攀缘纤维反应有微弱减弱外,对两者均无影响。因此,NAS为从药理学上区分平行纤维和攀缘纤维突触提供了一种有用的工具。