Ennis C, Minchin M C
Department of Biomedical Research, Wyeth Research Ltd, Berkshire, U.K.
Neuropharmacology. 1988 Oct;27(10):1003-6. doi: 10.1016/0028-3908(88)90059-7.
The effects of various benzodiazepine receptor ligands on the GABA autoreceptor have been studied in slices of cerebral cortex of the rat. The GABAA receptor agonist muscimol inhibited the K+-stimulated release of [3H]GABA with a pIC25 of 7.65 +/- 0.11. This effect was antagonised by the GABAA receptor antagonist bicuculline, which had an IC50 of 0.36 +/- 0.03 microM. Small concentrations (less than 1 microM) of the benzodiazepine full agonist clonazepam did not significantly alter K+-evoked release of [3H]GABA but shifted the concentration-effect curve for muscimol to the left. This effect was blocked by the benzodiazepine antagonist flumazenil. By contrast, the benzodiazepine full inverse agonist methyl beta-carboline-3-carboxylate shifted the muscimol concentration-effect curve to the right and this too was blocked by flumazenil. The results suggest that the GABA autoreceptor in cortical slices from the rat is modulated by a benzodiazepine receptor.
已在大鼠大脑皮质切片中研究了各种苯二氮䓬受体配体对GABA自身受体的影响。GABAA受体激动剂蝇蕈醇抑制K⁺刺激的[³H]GABA释放,其pIC₂₅为7.65±0.11。这种作用被GABAA受体拮抗剂荷包牡丹碱拮抗,其IC₅₀为0.36±0.03微摩尔。低浓度(小于1微摩尔)的苯二氮䓬完全激动剂氯硝西泮不会显著改变K⁺诱发的[³H]GABA释放,但会使蝇蕈醇的浓度-效应曲线左移。这种作用被苯二氮䓬拮抗剂氟马西尼阻断。相比之下,苯二氮䓬完全反向激动剂β-咔啉-3-羧酸甲酯使蝇蕈醇浓度-效应曲线右移,这也被氟马西尼阻断。结果表明,大鼠皮质切片中的GABA自身受体受苯二氮䓬受体调节。