Collins G G, Anson J
Neuropharmacology. 1987 Feb-Mar;26(2-3):167-71. doi: 10.1016/0028-3908(87)90205-x.
A study has been made of the effects of ranges of concentrations of phenobarbitone, pentobarbitone and thiopentone on responses evoked by gamma-aminobutyric acid (GABA), L-glutamate, L-aspartate, N-methyl-D-aspartate, kainate and quisqualate in slices of olfactory cortex of the rat. All three barbiturates affected GABA-evoked depolarizations similarly in that responses were potentiated by small doses but markedly inhibited at greater concentrations. Responses to L-aspartate and L-glutamate were little affected except at the largest dose of phenobarbitone tested (10 mM). The responses evoked by the selective agonists of excitatory amino acid receptors were inhibited by the barbiturates, the relative sensitivities being quisqualate greater than or equal to N-methyl-D-aspartate greater than or equal to kainate with phenobarbitone, quisqualate greater than or equal to kainate greater than N-methyl-D-aspartate with pentobarbitone and quisqualate greater than kainate = N-methyl-D-aspartate with thiopentone. The possible significance of these findings is discussed.
研究了苯巴比妥、戊巴比妥和硫喷妥钠不同浓度范围对大鼠嗅皮质切片中γ-氨基丁酸(GABA)、L-谷氨酸、L-天冬氨酸、N-甲基-D-天冬氨酸、 kainate和quisqualate所诱发反应的影响。所有三种巴比妥类药物对GABA诱发的去极化作用影响相似,即小剂量时反应增强,但在较高浓度时则明显受到抑制。对L-天冬氨酸和L-谷氨酸的反应影响很小,除非测试的苯巴比妥最大剂量(10 mM)。兴奋性氨基酸受体选择性激动剂所诱发的反应受到巴比妥类药物的抑制,相对敏感性为:苯巴比妥时 quisqualate≥N-甲基-D-天冬氨酸≥kainate,戊巴比妥时quisqualate≥kainate>N-甲基-D-天冬氨酸,硫喷妥钠时quisqualate>kainate = N-甲基-D-天冬氨酸。讨论了这些发现的可能意义。