Kita T, Kita H, Kitai S T
Brain Res. 1985 Dec 23;360(1-2):304-10. doi: 10.1016/0006-8993(85)91246-6.
Gamma-aminobutyric acid (GABA)ergic responses evoked by electrical stimulation in the neostriatal slice preparation were studied in neurons injected intracellularly with Na-conductance blocker QX-314. Local stimulation elicited depolarizing postsynaptic potentials (DPSPs) in the QX-314-injected neurons when the membrane potential was more negative than -60 mV. When DPSPs were minimized by depolarizing current injection in the QX-314-injected neuron, hyperpolarization was clearly observed following local stimulation. The maximum duration of the hyperpolarizing response to strong local stimulation was about 130 ms. The hyperpolarizing response was blocked by the addition of bicuculline or picrotoxin to the Ringer solution. Intracellular Cl- injections produced changes in the pattern of the local stimulation-induced responses; the initial depolarizing response was followed by a relatively large amplitude long duration depolarization. The polarity of the long duration depolarizing response could not be reversed by depolarizing currents which were normally sufficient to reverse the polarity of DPSPs in the neurons without Cl- injection. The application of pentobarbital enhanced the amplitude and the duration of the hyperpolarizing responses. The reversal potential of the pentobarbital-enhanced response was estimated to be -60 mV. On the basis of their reversal potential, sensitivity to injected Cl-, sensitivity to GABA blockers picrotoxin and bicuculline, and the effect of pentobarbital, these hyperpolarizing responses are shown to be GABAergic Cl-mediated inhibitory postsynaptic potentials (IPSPs).
在向细胞内注射钠电导阻滞剂QX - 314的神经元中,研究了新纹状体脑片制备中电刺激诱发的γ-氨基丁酸(GABA)能反应。当膜电位比 - 60 mV更负时,局部刺激在注射QX - 314的神经元中诱发去极化突触后电位(DPSP)。当通过向注射QX - 314的神经元中注入去极化电流使DPSP最小化时,局部刺激后可明显观察到超极化。对强局部刺激的超极化反应的最大持续时间约为130毫秒。向林格氏液中添加荷包牡丹碱或苦味毒可阻断超极化反应。细胞内注射Cl⁻会使局部刺激诱导的反应模式发生变化;最初的去极化反应之后是相对较大幅度、长时间的去极化。长时间去极化反应的极性不能被通常足以逆转未注射Cl⁻的神经元中DPSP极性的去极化电流所逆转。戊巴比妥的应用增强了超极化反应的幅度和持续时间。戊巴比妥增强反应的反转电位估计为 - 60 mV。基于它们的反转电位、对注射Cl⁻的敏感性、对GABA阻滞剂苦味毒和荷包牡丹碱的敏感性以及戊巴比妥的作用,这些超极化反应被证明是GABA能Cl⁻介导的抑制性突触后电位(IPSP)。