Nicoll R A, Madison D V
Science. 1982 Sep 10;217(4564):1055-7. doi: 10.1126/science.7112112.
The effect of general anesthetics on frog motoneurons and rat hippocampus pyramidal cells was examined with sucrose gap and intracellular recording, respectively. A number of volatile and intravenous anesthetics directly hyperpolarized the motoneurons. The potency of these agents in hyperpolarizing motoneurons was strongly correlated with their anesthetic potency. While the responses to barbiturates and alpha-chloralose were blocked by gamma-aminobutyric acid antagonists and were dependent on the chloride gradient, the responses to all the other anesthetics tested were generated by a separate mechanism. Intracellular recording from hippocampal pyramidal cells suggested that an increase in potassium conductance accounts for these responses. Such a nonsynaptic action would contribute to the decreased neuronal responsiveness observed for these compounds and thus to their anesthetic action.
分别采用蔗糖间隙法和细胞内记录法,研究了全身麻醉药对青蛙运动神经元和大鼠海马锥体细胞的作用。多种挥发性和静脉麻醉药可直接使运动神经元超极化。这些药物使运动神经元超极化的效力与其麻醉效力密切相关。虽然对巴比妥类药物和α-氯醛糖的反应可被γ-氨基丁酸拮抗剂阻断,且依赖于氯离子梯度,但对所有其他测试麻醉药的反应是由另一种机制产生的。海马锥体细胞的细胞内记录表明,钾电导增加是这些反应的原因。这种非突触作用将导致这些化合物所观察到的神经元反应性降低,从而促成其麻醉作用。