Funk D, Li Z, Fletcher P J, Lê A D
Department of Neuroscience, Center for Addiction and Mental Health, Toronto, Ontario, Canada M5S 2S1.
Neuroscience. 2005;131(2):475-9. doi: 10.1016/j.neuroscience.2004.11.026.
Inhibition of the median raphe nucleus (MRN) by the local injection of 5-HT(1A) or GABA(A) receptor agonists produces strong activational effects on feeding, drinking and locomotor activity. Using an animal model of relapse, we have shown that intra-MRN injection of the 5-HT(1A) autoreceptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) reinstates alcohol seeking in rats. The circuitry underlying the behavioral effects of intra-MRN injection of these drugs is not known. In order to identify the brain areas that may be involved, we measured levels of mRNA of the immediate early gene c-fos in discrete nuclei of the rat brain following intra-MRN infusions of these drugs. Male Wistar rats received intra-MRN infusions of 8-OH-DPAT (1 mug), muscimol (25 ng) or saline vehicle immediately prior to placement in locomotor activity chambers. Thirty minutes later, they were decapitated, and their brains processed for in situ hybridization of c-fos mRNA. In agreement with previous reports, injections of 8-OH-DPAT or muscimol into the MRN resulted in large increases in locomotor activity. Intra-MRN injections of these drugs increased c-fos in a number of brain nuclei previously shown to be involved in the rewarding effects of drugs of abuse in a regionally specific manner. Both drugs significantly increased the expression of c-fos mRNA in the medial frontal cortex, nucleus accumbens, lateral septum, dorsal bed nucleus of the stria terminalis and ventral tegmental area. In the ventral hippocampus, only 8-OH-DPAT increased c-fos, while in the basolateral nucleus of the amygdala and locus coeruleus, it was increased only by muscimol. These results are discussed in terms of the projections of the MRN and the pathways involved in relapse to alcohol and drug seeking.
在中缝正中核(MRN)局部注射5-羟色胺(1A)或γ-氨基丁酸(A)受体激动剂可对进食、饮水和运动活动产生强烈的激活作用。利用复发动物模型,我们已经证明向MRN内注射5-羟色胺(1A)自身受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)可使大鼠恢复觅酒行为。向MRN内注射这些药物所产生行为效应的神经回路尚不清楚。为了确定可能涉及的脑区,我们在向MRN内注入这些药物后,测量了大鼠脑内离散核团中即早基因c-fos的mRNA水平。雄性Wistar大鼠在被放入运动活动箱之前,立即向MRN内注入8-OH-DPAT(1微克)、蝇蕈醇(25纳克)或生理盐水。30分钟后,将它们断头,并对其大脑进行c-fos mRNA的原位杂交处理。与先前的报道一致,向MRN内注射8-OH-DPAT或蝇蕈醇会导致运动活动大幅增加。向MRN内注射这些药物会以区域特异性方式使先前已证明参与滥用药物奖赏效应的多个脑核中的c-fos增加。两种药物均显著增加了内侧前额叶皮质、伏隔核、外侧隔区、终纹床核背侧部和腹侧被盖区中c-fos mRNA的表达。在腹侧海马中,只有8-OH-DPAT增加了c-fos,而在杏仁核基底外侧核和蓝斑中,只有蝇蕈醇增加了c-fos。根据MRN的投射以及与酒精复发和觅药相关的通路对这些结果进行了讨论。