Niles L P, Pickering D S, Arciszewski M A
Department of Neurosciences, McMaster University, Hamilton, Ontario, Canada.
J Neural Transm. 1987;70(1-2):117-24. doi: 10.1007/BF01252513.
In order to determine whether the in vitro ability of the pineal indoleamine hormone, melatonin, to modulate binding at the GABA-benzodiazepine receptor complex is operative in vivo we have examined the effects of chronic melatonin administration on 3H-GABA and 3H-diazepam binding in rat brain. Melatonin was injected daily in increasing doses for three weeks and animals were sacrificed at 2 or 26 hours after the final injection. A melatonin-induced enhancement of 3H-GABA binding was observed in both single-point and saturation binding experiments. Scatchard analysis of 3H-diazepam binding revealed a melatonin-induced increase in binding affinity at 26 hours in the forebrain and at 2 hours in the cerebellum with no significant changes in binding site concentration. These findings are consistent with the proposal that melatonin's psychopharmacological effects are due at least in part to its ability to enhance central GABAergic transmission by modulating GABA receptor activity.
为了确定松果体吲哚胺激素褪黑素在体外调节γ-氨基丁酸-苯二氮䓬受体复合物结合的能力在体内是否起作用,我们研究了长期给予褪黑素对大鼠脑内3H-γ-氨基丁酸和3H-地西泮结合的影响。以递增剂量每日注射褪黑素,持续三周,在最后一次注射后2小时或26小时处死动物。在单点和饱和结合实验中均观察到褪黑素诱导的3H-γ-氨基丁酸结合增强。对3H-地西泮结合的Scatchard分析显示,褪黑素在26小时时诱导前脑结合亲和力增加,在2小时时诱导小脑结合亲和力增加,结合位点浓度无显著变化。这些发现与以下观点一致,即褪黑素的心理药理学作用至少部分归因于其通过调节γ-氨基丁酸受体活性来增强中枢γ-氨基丁酸能传递的能力。