Okuyama S, Shimamura H, Hashimoto S, Aihara H
Arch Int Pharmacodyn Ther. 1986 Dec;284(2):246-54.
Single neuronal activity was recorded extracellularly in the substantia nigra pars compacta (SNC) in rats anesthetized with chloral hydrate. Haloperidol in a dose of 10 micrograms/kg had no significant effects on the SNC neurons. R(-)apomorphine (cumulative i.v. dose of 40 micrograms/kg, given as: 5, 5, 10 and 20 micrograms/kg) inhibited the firing rate of dopaminergic neurons, in a dose-dependent manner. Haloperidol (cumulative i.v. dose of 10 micrograms/kg, as: 2.5, 2.5 and 5 micrograms/kg) reversed the effect of apomorphine. Complete reversal of the firing rate to haloperidol was observed with a dose of 10 micrograms/kg. In rats pretreated with 10 micrograms/kg of haloperidol, there was a dramatic shift to the right of the apomorphine dose-response curve (cumulative i.v. dose of 800 micrograms/kg, as: 50, 50, 100, 200 and 400 micrograms/kg), and this inhibition was reversed by haloperidol (cumulative i.v. dose of 400 micrograms/kg, as: 50, 50, 100 and 200 micrograms/kg). Apomorphine in doses of 40 micrograms/kg and 800 micrograms/kg elicited yawning behavior and stereotypy, respectively. Apomorphine in a dose of 800 micrograms/kg elicited stereotypy in rats treated 3 min before with 10 micrograms/kg of haloperidol. Therefore, electrophysiological determinations of events in the SNC dopaminergic neurons are given support by the behavior observed in these rats.
在水合氯醛麻醉的大鼠中,细胞外记录黑质致密部(SNC)的单个神经元活动。剂量为10微克/千克的氟哌啶醇对SNC神经元无显著影响。R(-)阿扑吗啡(静脉累积剂量为40微克/千克,给药方式为:5、5、10和20微克/千克)以剂量依赖性方式抑制多巴胺能神经元的放电率。氟哌啶醇(静脉累积剂量为10微克/千克,给药方式为:2.5、2.5和5微克/千克)可逆转阿扑吗啡的作用。观察到剂量为10微克/千克时,放电率完全恢复至氟哌啶醇作用前水平。在用10微克/千克氟哌啶醇预处理的大鼠中,阿扑吗啡剂量-反应曲线(静脉累积剂量为800微克/千克,给药方式为:50、50、100、200和400微克/千克)显著右移,且这种抑制作用可被氟哌啶醇(静脉累积剂量为400微克/千克,给药方式为:50、50、100和200微克/千克)逆转。剂量为40微克/千克和800微克/千克的阿扑吗啡分别引发打哈欠行为和刻板行为。在提前3分钟用10微克/千克氟哌啶醇处理的大鼠中,剂量为800微克/千克的阿扑吗啡引发刻板行为。因此,这些大鼠的行为观察结果支持了对SNC多巴胺能神经元事件的电生理测定。