Lorden J F, Callahan M, Dawson R
J Comp Physiol Psychol. 1980 Feb;94(1):99-114. doi: 10.1037/h0077650.
Conditioned taste aversions induced by pairing the consumption of saccharin with an amphetamine injection are attenuated in rats with depletion of central catecholamines caused by intraventricular administration of 6-hydroxydopamine (6-OHDA). The hypothesis that dopamine (DA) depletion is responsible for this effect was tested. The reduction in conditioning caused by intraventricular 6-OHDA could not be duplicated either with injections of 6-OHDA into the substantia nigra (Experiment 1) or with intraventricular 6-OHDA injections in animals pretreated with desmethylimipramine (Experiment 2). Both treatments, however, produced large depletions of telencephalic DA. 6-Hydroxydopa infusions caused a preferential loss of telencephalic norepinephrine (NE) but also failed to alter taste aversion learning. It is concluded that the effect of intraventricular 6-OHDA on amphetamine-induced aversions was the result of depletion of both NE and DA. In a third experiment the generality of the effect was examined by pairing saccharin consumption with injections of the amphetamine congener fenfluramine. Depletion of both NE and DA failed to alter fenfluramine-induced aversions. Infusion of 6-OHDA into the substantia nigra, however, retarded the extinction of such an aversion. Evidence is discussed for a peripheral site of action for fenfluramine in the conditioned aversion paradigm.
通过将糖精的摄入与苯丙胺注射配对诱导的条件性味觉厌恶,在通过脑室内注射6-羟基多巴胺(6-OHDA)导致中枢儿茶酚胺耗竭的大鼠中会减弱。检验了多巴胺(DA)耗竭是造成这种效应的原因这一假设。脑室内注射6-OHDA所导致的条件作用的降低,既不能通过向黑质注射6-OHDA(实验1)来复制,也不能通过在预先用去甲丙咪嗪处理的动物中进行脑室内6-OHDA注射来复制(实验2)。然而,这两种处理都导致了端脑DA的大量耗竭。6-羟基多巴输注导致端脑去甲肾上腺素(NE)优先丧失,但也未能改变味觉厌恶学习。得出的结论是,脑室内6-OHDA对苯丙胺诱导的厌恶的影响是NE和DA两者耗竭的结果。在第三个实验中,通过将糖精的摄入与苯丙胺同系物芬氟拉明的注射配对来检验这种效应的普遍性。NE和DA的耗竭未能改变芬氟拉明诱导的厌恶。然而,向黑质注射6-OHDA会延缓这种厌恶的消退。讨论了在条件性厌恶范式中芬氟拉明的外周作用位点的证据。