Collinge J, Pycock C
Eur J Pharmacol. 1982 Nov 5;85(1):9-14. doi: 10.1016/0014-2999(82)90418-6.
The possible interaction of the benzodiazepine diazepam with synaptic mechanisms of the central neurotransmitter 5-hydroxytryptamine (5-HT) has been studied in the rat using the superfusion in vitro release technique. The effect of diazepam (1-100 microM) on the spontaneous and potassium-induced release of radioactivity from superfused slices preloaded with [3H]5-HT prepared from cerebral cortex (fronto-parietal) and midbrain raphe region was monitored and compared. The results demonstrate a differential action of diazepam on the release of cortical and raphe 5-HT. In cerebral cortex diazepam significantly reduces both spontaneous and potassium-evoked release of [3H]5-HT. Conversely in raphe slices diazepam significantly enhances both spontaneous and potassium-evoked release of [3H]5-HT. In both tissues the effect of diazepam on K+-stimulated neurotransmitter release was abolished in the presence of picrotoxin. The experiments suggest that the effects of benzodiazepines on 5-HT mechanisms may be manifested at least in part through gamma-aminobutyric acid receptors.
利用体外灌流释放技术,在大鼠身上研究了苯二氮䓬类药物地西泮与中枢神经递质5-羟色胺(5-HT)突触机制之间可能存在的相互作用。监测并比较了地西泮(1-100微摩尔)对由大脑皮层(额顶叶)和中脑缝际区制备的预先加载[3H]5-HT的灌流切片中放射性物质的自发释放和钾诱导释放的影响。结果表明,地西泮对皮层和缝际区5-HT的释放具有不同的作用。在大脑皮层中,地西泮显著降低了[3H]5-HT的自发释放和钾诱发释放。相反,在缝际切片中,地西泮显著增强了[3H]5-HT的自发释放和钾诱发释放。在两种组织中,在存在苦味毒的情况下,地西泮对钾刺激的神经递质释放的作用均被消除。这些实验表明,苯二氮䓬类药物对5-HT机制的影响可能至少部分通过γ-氨基丁酸受体表现出来。