Nieoullon A, Cheramy A, Leviel V, Glowinski J
Eur J Pharmacol. 1979 Jan 15;53(3):289-96. doi: 10.1016/0014-2999(79)90135-3.
The effects of the unilateral application of d-amphetamine, benztropine, haloperidol and thioproperazine to one substantia nigra on the release of 3H-dopamine (3H-DA) in the two caudate nuclei were examined in halothane-anesthetized cats. For this purpose animals were implanted with push-pull cannulae and 3H-DA was estimated in superfusates during the continuous delivery of L-3,5-3H-tyrosine. The nigral application of d-amphetamine (10-6 M) or benztropine (10-6 M) reduced the release of 3-H-DA in in the ipsilateral caudate nucleus and induced an opposite effect in the contralateral side. In contrast, the nigral application of haloperidol (10-6 M) or thioproperazine (10-6 M) slightly increased the release of 3H-DA in the ipsilateral caudate nucleus and induced a reduction of 3H-transmitter release in the contralateral side. These results emphasize the role of the dendritic release of DA in the control of the activity of dopaminergic neurons and confirm our previous findings concerning the existence of a reciprocal control in the activity of the two dopaminergic pathways.
在氟烷麻醉的猫中,研究了向一侧黑质单侧应用d-苯丙胺、苯海索、氟哌啶醇和硫丙嗪对双侧尾状核中3H-多巴胺(3H-DA)释放的影响。为此,给动物植入推挽式套管,并在持续输注L-3,5-3H-酪氨酸期间,估计灌流液中的3H-DA。向黑质应用d-苯丙胺(10-6M)或苯海索(10-6M)可减少同侧尾状核中3-H-DA的释放,并在对侧产生相反的作用。相反,向黑质应用氟哌啶醇(10-6M)或硫丙嗪(10-6M)可使同侧尾状核中3H-DA的释放略有增加,并导致对侧3H-递质释放减少。这些结果强调了多巴胺树突状释放对多巴胺能神经元活动控制的作用,并证实了我们先前关于两条多巴胺能通路活动中存在相互控制的发现。