Snead O C
Neuropharmacology. 1982 Jun;21(6):539-43. doi: 10.1016/0028-3908(82)90044-2.
An investigation was made into the relationship between dopaminergic and EEG effects of gamma-butyrolactone (GBL) by comparing time-course and dose-response studies of these two actions of gamma-butyrolactone in rats implanted with permanent cortical electrodes. Dopaminergic effects were assessed by the changes induced by gamma-butyrolactone in the concentration of dopamine and dihydroxyphenylacetic acid (DOPAC) in the striatum and cortex. In addition, the effects of anticonvulsant drugs, known to overcome the EEG effects of gamma-butyrolactone, were assessed against the dopaminergic actions of this drug. The EEG changes induced by gamma-butyrolactone occurred with smaller doses, had an earlier onset and lasted longer than the elevation in striatal dopamine and DOPAC concentration induced by gamma-butyrolactone. There were marked sequential changes in EEG and behavior in the face of normal dopamine and DOPAC concentrations in animals given 200 mg/kg of gamma-butyrolactone. The anticonvulsants, ethosuximide and trimethadione, which abolish or attenuate seizure activity induced by gamma-butyrolactone, were effective in aborting or decreasing the rise in striatal dopamine concentration produced by gamma-butyrolactone. However, sodium valproate, also known to abolish or attenuate the EEG effects of gamma-butyrolactone exacerbated the dopamine effects of this compound. The elevation in dopamine produced by gamma-butyrolactone does not seem to be responsible for the EEG or behavioral effects seen with this substance.
通过比较γ-丁内酯(GBL)在植入永久性皮质电极的大鼠体内这两种作用的时程和剂量反应研究,对γ-丁内酯的多巴胺能效应与脑电图(EEG)效应之间的关系进行了研究。通过γ-丁内酯引起的纹状体和皮质中多巴胺和二羟基苯乙酸(DOPAC)浓度的变化来评估多巴胺能效应。此外,评估了已知能克服γ-丁内酯EEG效应的抗惊厥药物对该药物多巴胺能作用的影响。γ-丁内酯引起的EEG变化所需剂量较小,起效较早且持续时间比γ-丁内酯引起的纹状体多巴胺和DOPAC浓度升高更长。给予200mg/kgγ-丁内酯的动物在多巴胺和DOPAC浓度正常的情况下,EEG和行为出现明显的顺序性变化。抗惊厥药乙琥胺和三甲双酮可消除或减弱γ-丁内酯诱导的癫痫活动,它们能有效中止或降低γ-丁内酯引起的纹状体多巴胺浓度升高。然而,同样已知能消除或减弱γ-丁内酯EEG效应的丙戊酸钠却加剧了该化合物的多巴胺效应。γ-丁内酯引起的多巴胺升高似乎不是该物质所产生的EEG或行为效应的原因。