Daudet F, Leviel V, Kerny C, Guibert B, Barberis C
Eur J Pharmacol. 1983 Nov 25;95(3-4):199-205. doi: 10.1016/0014-2999(83)90635-0.
Simultaneously with a systemic injection of naloxone (NAL), the effects of the nigral application of the d(+)-amphetamine (AMPH) or of right forepaw stimulation on the release of [3H]dopamine [( 3H]DA) in the two caudate nuclei (CN) and the two substantia nigrae (SN) were examined in halothane-anesthetized cats. These experiments were carried out using four push-pull cannulae implanted bilaterally in the CN and SN and continuously supplied with [3H]tyrosine [( 3H]Tyr), the metabolic precursor of dopamine. Nigral AMPH application (1 muM) produced a local increase of the [3H]DA in spite of the NAL injection (5 mg/kg) but the presence of this drug prevented the expected effect of AMPH in the three other structures. Furthermore, the effects of electrical forepaw stimulation (EPS) were abolished by injection of NAL. NAL alone had no effect on the spontaneous release of [3H]DA. It is concluded that antagonism between NAL and AMPH could be due: (1) to enkephalinergic control of dopamine regulated nigral efferents, (2) to an action on the thalamic structures responsible for the reciprocal control of the two nigrostriatal dopaminergic pathways.
在氟烷麻醉的猫中,同时进行纳洛酮(NAL)的全身注射,研究了黑质应用d(+)-苯丙胺(AMPH)或右前爪刺激对两个尾状核(CN)和两个黑质(SN)中[3H]多巴胺[(3H]DA)释放的影响。这些实验是通过在双侧CN和SN中植入四个推挽式套管进行的,并持续供应多巴胺的代谢前体[3H]酪氨酸[(3H]Tyr)。尽管注射了NAL(5mg/kg),黑质应用AMPH(1μM)仍使[3H]DA局部增加,但该药物的存在阻止了AMPH在其他三个结构中的预期作用。此外,注射NAL消除了电刺激前爪(EPS)的作用。单独使用NAL对[3H]DA的自发释放没有影响。得出的结论是,NAL和AMPH之间的拮抗作用可能是由于:(1)脑啡肽能对多巴胺调节的黑质传出神经的控制,(2)对负责两条黑质纹状体多巴胺能通路相互控制的丘脑结构的作用。