首页> 外文期刊>Neuropharmacology >In vitro modulation of the firing rate of dopamine neurons in the rat substantia nigra pars compacta and the ventral tegmental area by antipsychotic drugs.
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In vitro modulation of the firing rate of dopamine neurons in the rat substantia nigra pars compacta and the ventral tegmental area by antipsychotic drugs.

机译:抗精神病药对大鼠黑质致密部和腹侧被盖区多巴胺神经元放电速率的体外调节。

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摘要

An in vitro experimental midbrain slice preparation is described which allows simultaneous extracellular recordings of the (spontaneous) electrical activity of dopamine neurons in the rat substantia nigra (SN) and the ventral tegmental area (VTA). Under identical in vitro circumstances the mean firing frequency of the SN dopamine neurons was higher than that of the VTA dopamine neurons (2.1 vs. 1.4Hz). With this slice preparation, modulation of the electrical activity of SN and VTA dopamine neurons by (new) drugs can be quickly determined. Experiments with the selective D2 receptor agonist quinpirole and the selective D2 receptor antagonist (-)-sulpiride indicated that dopamine neurons in the SN and VTA hardly differ in their pharmacological properties for the D2-like (auto)receptor. (-)-Sulpiride and to a lesser extent risperidone induced a small increase in firing rate in SN and VTA neurons, which was reversible upon wash-out. Olanzapine-induced increase in firing rate was persistent in SN and VTA neurons, whereas the clozapine-induced increase in firing rate was only completely recovered upon wash-out in SN neurons. The difference in firing rates of SN and VTA dopamine neurons could have consequences for the effectiveness of dopaminergic drugs acting at the D2-like dopamine (auto)receptor on these neurons.
机译:描述了体外实验中脑切片制剂,其允许同时记录大鼠黑质(SN)和腹侧被盖区(VTA)中多巴胺神经元的(自发)电活动。在相同的体外条件下,SN多巴胺神经元的平均激发频率高于VTA多巴胺神经元(2.1与1.4Hz)。通过这种切片准备,可以快速确定(新)药物对SN和VTA多巴胺神经元电活动的调节。用选择性D2受体激动剂喹吡罗和选择性D2受体拮抗剂(-)-舒必利进行的实验表明,SN和VTA中的多巴胺神经元对D2样(自身)受体的药理特性几乎没有差异。 (-)-舒必利和利培酮在较小程度上引起SN和VTA神经元放电速率的小幅增加,这在洗脱后是可逆的。奥氮平诱导的放电率在SN和VTA神经元中持续存在,而氯氮平诱导的放电率仅在SN神经元被冲刷后才能完全恢复。 SN和VTA多巴胺神经元放电速度的差异可能会对作用在这些神经元上的D2样多巴胺(自身)受体的多巴胺能药物的有效性产生影响。

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