Heidbreder C, Feldon J
Swiss Federal Institute of Technology Zürich (ETH), Institute of Toxicology, Schwerzenbach, Switzerland.
Synapse. 1998 Aug;29(4):310-22. doi: 10.1002/(SICI)1098-2396(199808)29:4<310::AID-SYN3>3.0.CO;2-8.
The administration of psychostimulants increases dopamine (DA) release within the nucleus accumbens (NAC), a terminal projection site of mesolimbic DA neurons, originating in the ventral tegmental area (VTA). Recent evidence demonstrates that two subdivisions of the NAC, the dorsolateral core and the ventromedial shell, can be distinguished by morphological and immunohistochemical differences, as well as by their distinct anatomical connections. It has been suggested that these two subregions subserve different functions that are related to goal-directed behaviors, stimulus-reward associations, and reinforcement induced by addictive drugs. The shell region, in particular, modulates inputs from the limbic system, whereas the core is preferentially innervated by nuclei that process motor information. In the present study, we sought to investigate if (1) the direct infusion of d-amphetamine (AMPH) by reverse microdialysis into either the core or shell of the NAC across its anteroposterior axis differentially affects dialysate DA and 5-HT levels, and (2) these subterritories also subserve different behavioral functions. Following the determination of basal DA and 5-HT levels, four increasing concentrations of AMPH (0.05, 0.10, 0.50, 1.00 microM) were substituted for the dialysis perfusate for 60 min each. Movement units were detected by an infrared sensor and were transmitted through a motion interface to an activity monitor analyzer. AMPH produced a dose-dependent increase in locomotor activity after microinfusion into either the rostral shell, caudal shell or core of the NAC. The potency of the AMPH-induced locomotor activating effect was significantly higher in the rostral shell of the NAC compared with the caudal shell and the core. The lowest concentrations of AMPH (0.05, 0.1 microM) produced an equipotent decrease in dialysate DA in either the rostral shell, caudal shell, or core. At 1.0 microM, however, AMPH selectively increased DA in the rostral shell, whereas DA reached baseline values both in the caudal shell and core. Basal dialysate DA levels were significantly higher in the core relative to both the rostral and caudal parts of the shell. The highest dose of AMPH significantly increased dialysate 5-HT levels over baseline only in the caudal shell of the NAC. The basal dialysate 5-HT levels did not significantly differ between the three subterritories of the NAC. These results emphasize the heterogeneity and functional compartmentalization within the NAC, the differential regulation of neurochemical and motor responses across the anteroposterior axis of the NAC, and the preferential effect of AMPH in the rostral shell subterritory of the NAC.
精神兴奋剂的施用会增加伏隔核(NAC)内的多巴胺(DA)释放,伏隔核是中脑边缘多巴胺能神经元的终末投射部位,起源于腹侧被盖区(VTA)。最近的证据表明,NAC的两个亚区,即背外侧核和腹内侧壳,可以通过形态学和免疫组织化学差异以及它们独特的解剖学连接来区分。有人提出,这两个亚区发挥着与目标导向行为、刺激-奖励关联以及成瘾药物诱导的强化作用相关的不同功能。特别是壳区调节来自边缘系统的输入,而核区则优先接受处理运动信息的核团的支配。在本研究中,我们试图探究:(1)通过反向微透析将d-苯丙胺(AMPH)直接注入NAC沿前后轴的核区或壳区是否会对透析液中的DA和5-羟色胺(5-HT)水平产生不同影响;(2)这些亚区域是否也发挥不同的行为功能。在测定基础DA和5-HT水平后,用四种递增浓度的AMPH(0.05、0.10、0.50、1.00微摩尔)分别替代透析灌注液60分钟。运动单元通过红外传感器检测,并通过运动接口传输到活动监测分析仪。将AMPH微注入NAC的吻侧壳区、尾侧壳区或核区后,均产生了剂量依赖性的运动活动增加。与尾侧壳区和核区相比,AMPH诱导的运动激活效应在NAC吻侧壳区的效力显著更高。最低浓度的AMPH(0.05、0.1微摩尔)在吻侧壳区、尾侧壳区或核区均使透析液DA等量减少。然而,在1.0微摩尔时,AMPH选择性地增加了吻侧壳区的DA,而尾侧壳区和核区的DA均恢复到基线值。相对于壳区的吻侧和尾侧部分,核区的基础透析液DA水平显著更高。仅在NAC的尾侧壳区,最高剂量的AMPH使透析液5-HT水平显著高于基线。NAC的三个亚区域之间的基础透析液5-HT水平无显著差异。这些结果强调了NAC内的异质性和功能分区、NAC沿前后轴对神经化学和运动反应的差异调节,以及AMPH在NAC吻侧壳区亚区域的优先作用。