Huang L Y, Barker J L
Science. 1980 Jan 11;207(4427):195-7. doi: 10.1126/science.7350656.
Stereoisomers of the barbiturate anesthetic pentobarbital were applied to mouse spinal neurons growing in tissue culture. Intracellular recordings of neuronal membrane properties revealed that the (+) and (-) isomers caused direct changes in membrane potential and conductance on some but not all of the cells tested. The action of the (+) isomer was predominantly excitatory, whereas the (-) isomer produced predominantly inhibitory responses. The (-) isomer was considerably more effective in potentiating inhibitory responses to the transmitter gamma-aminobutyric acid. The results show that pentobarbital has multiple effects on neuronal excitability and demonstrate the presence of stereospecific sites of barbiturate action on central neurons.
将巴比妥类麻醉剂戊巴比妥的立体异构体应用于在组织培养中生长的小鼠脊髓神经元。对神经元膜特性的细胞内记录显示,(+)和(-)异构体在部分而非全部测试细胞上引起膜电位和电导的直接变化。(+)异构体的作用主要是兴奋性的,而(-)异构体主要产生抑制性反应。(-)异构体在增强对递质γ-氨基丁酸的抑制性反应方面更为有效。结果表明,戊巴比妥对神经元兴奋性有多种作用,并证明巴比妥类药物在中枢神经元上存在立体特异性作用位点。