Dudel J
Pflugers Arch. 1975;356(4):317-27. doi: 10.1007/BF00580005.
Glutamate was applied iontophoretically in short (10 to 20 ms) pulses through micropipettes of 10 to 30 M Omega resistance to synaptic spots on crayfish muscle fibres. The resulting glutamate induced postsynaptic currents (gEPSCs) were measured using a voltage clamp of the muscle fiber. Dose-response curves for the action of glutamate were constructed summing g-EPSCs elicited by two separate iontophoretic pipettes at the same synapse. The dose-response curves showed a log log slope of 2, the g-EPSC rising with the second power of the glutamate concentration. Following a small conditioning g-EPSC with delay of up to 1 s, a second g-EPSC was potentiated. For short delays maximum potentiation was 3-fold. For large g-EPSCs potentiation gave way to desensitization: following a large conditioning gEPSC a second one was reduced for delays of up to several seconds. Possible mechanisms of potentiation and desensitization are discussed.
通过电阻为10至30兆欧的微吸管,以短脉冲(10至20毫秒)离子电泳方式将谷氨酸施加到小龙虾肌肉纤维上的突触位点。使用肌肉纤维电压钳测量由此产生的谷氨酸诱导的突触后电流(gEPSCs)。通过对同一突触处两个独立离子电泳吸管引发的g-EPSCs求和,构建谷氨酸作用的剂量反应曲线。剂量反应曲线显示对数-对数斜率为2,g-EPSC随谷氨酸浓度的二次幂上升。在小的条件性g-EPSC之后,延迟长达1秒,第二个g-EPSC会增强。对于短延迟,最大增强倍数为3倍。对于大的g-EPSCs,增强作用会转变为脱敏作用:在一个大的条件性gEPSC之后,第二个g-EPSC在长达几秒的延迟后会减小。文中讨论了增强和脱敏的可能机制。