Pothuizen Helen H J, Jongen-Rêlo Ana L, Feldon Joram
Laboratory of Behavioural Neurobiology, Swiss Federal Institute of Technology Zurich, Schwerzenbach, Switzerland.
Neuropsychopharmacology. 2005 Apr;30(4):683-96. doi: 10.1038/sj.npp.1300643.
The nucleus accumbens can be dissociated into at least two subregions: a 'core' and a 'shell'. Using temporary chemical inactivation of these subregions, we investigated whether they are differentially involved in the regulation of prepulse inhibition (PPI) of the acoustic startle reflex and activity. For this purpose, rats were bilaterally implanted with guide cannulae aimed at either the core or the shell and infused with the GABA(A) receptor agonist muscimol (0.5 microg/0.2 microl per side). The control group consisted of vehicle infused and unoperated rats. To ascertain the region selectivity of the infusions, 0.2 microl of [3H]muscimol was infused into either the core or the shell of an additional group of rats. The behavioral results demonstrated that in comparison to the control group, inactivation of the core led to a loss of the prepulse intensity dependency of PPI. Moreover, core inactivation resulted in akinesia directly after infusion, but in hyperactivity 24 and 72 h thereafter in contrast to the control group. In both experiments, inactivation of the shell was ineffective compared to controls. Analysis of the autoradiograms revealed that the spread of drug into the other subregion was minimal, supporting the region selectivity of the inactivation. These results lend further support to the existence of a functional dissociation between the core and the shell, with the former being preferentially involved in PPI and locomotion. The persistent hyperactivity after the muscimol infusion into the core could be explained by compensatory mechanisms taking place in the nucleus accumbens.
“核心”和“壳”。利用这些亚区的临时化学失活,我们研究了它们是否在听觉惊吓反射的前脉冲抑制(PPI)和活动调节中发挥不同作用。为此,将大鼠双侧植入导向套管,分别针对核心或壳,并注入GABA(A)受体激动剂蝇蕈醇(每侧0.5微克/0.2微升)。对照组由注入溶剂且未手术的大鼠组成。为确定注入的区域选择性,向另一组大鼠的核心或壳中注入0.2微升[3H]蝇蕈醇。行为学结果表明,与对照组相比,核心失活导致PPI的前脉冲强度依赖性丧失。此外,核心失活在注入后直接导致运动不能,但与对照组相比,在24小时和72小时后导致多动。在两个实验中,壳失活与对照组相比无效。放射自显影片分析显示药物扩散到其他亚区的程度最小,支持失活的区域选择性。这些结果进一步支持了核心和壳之间存在功能分离,前者优先参与PPI和运动。向核心注入蝇蕈醇后持续的多动可由伏隔核中发生的代偿机制来解释。