Kaila K, Heinonen E, Akerman K E
Acta Physiol Scand. 1984 Dec;122(4):599-605. doi: 10.1111/j.1748-1716.1984.tb07549.x.
The effects of the convulsant drug 4-Cl phenol on synaptic transmission were studied in the opener muscle of the crayfish walking leg. 4-Cl phenol was found to increase the amplitude of the excitatory postsynaptic potential without affecting the resting potential or input resistance of the muscle fiber. The drug did not change the frequency of spontaneous miniature postsynaptic potentials in K+-depolarized fibers. The postsynaptic voltage response to bath-applied glutamate (the excitatory transmitter compound) was decreased while the Cl(-) -conductance increase related to the action of bath-applied gamma-aminobutyric acid (the inhibitory transmitter) was not affected. In the light of previous results obtained on crayfish axons it is concluded that convulsant phenols induce an increase in the evoked release of transmitter by increasing the duration of the presynaptic depolarization through a block of voltage-dependent potassium channels.
研究了惊厥药物4-氯苯酚对小龙虾步足 opener 肌突触传递的影响。发现4-氯苯酚可增加兴奋性突触后电位的幅度,而不影响肌纤维的静息电位或输入电阻。该药物不会改变钾离子去极化纤维中自发微小突触后电位的频率。对浴槽施加的谷氨酸(兴奋性递质化合物)的突触后电压反应降低,而与浴槽施加的γ-氨基丁酸(抑制性递质)作用相关的氯离子电导增加不受影响。根据先前在小龙虾轴突上获得的结果,得出结论:惊厥性酚类通过阻断电压依赖性钾通道增加突触前去极化的持续时间,从而诱导递质诱发释放增加。