Swain J E, Robitaille R, Dass G R, Charlton M P
Department of Physiology, University of Toronto, Ontario, Canada.
J Neurobiol. 1991 Nov;22(8):855-64. doi: 10.1002/neu.480220806.
We examined the role of phosphatases in synaptic transmission using the permeant phosphatase inhibitor okadaic acid (OA). In the crayfish neuromuscular junction (NMJ), postsynaptic effects including increases in input resistance occurred at doses greater than 5 microM OA. At lower doses (0.5-5 microM) the effects were solely presynaptic and transmitter release increased over three-fold despite small reductions in amplitude and duration of presynaptic action potentials. Potentiating effects of serotonin on transmitter release, which depend on phosphorylation, were increased by OA. Frequency facilitation was reduced but its decay was not affected. In frog NMJs, OA increased spontaneous and evoked release two-fold through presynaptic mechanisms. An inactive analog of OA, OA tetra-acetate, had no effect on transmitter release at frog and crayfish NMJ. Therefore, phosphatases have a strong modulating influence on synaptic transmission.
我们使用渗透性磷酸酶抑制剂冈田酸(OA)研究了磷酸酶在突触传递中的作用。在小龙虾神经肌肉接头(NMJ)中,当OA剂量大于5微摩尔时,会出现包括输入电阻增加在内的突触后效应。在较低剂量(0.5 - 5微摩尔)时,效应仅为突触前效应,尽管突触前动作电位的幅度和持续时间略有减小,但递质释放增加了三倍多。5-羟色胺对递质释放的增强作用(其依赖于磷酸化)因OA而增强。频率易化作用减弱,但其衰减不受影响。在青蛙神经肌肉接头中,OA通过突触前机制使自发释放和诱发释放增加了两倍。OA的无活性类似物OA四乙酸酯对青蛙和小龙虾神经肌肉接头的递质释放没有影响。因此,磷酸酶对突触传递具有强大的调节作用。