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首页> 外文期刊>Neuropsychopharmacology >The Effects of Temporary Inactivation of the Core and the Shell Subregions of the Nucleus Accumbens on Prepulse Inhibition of the Acoustic Startle Reflex and Activity in Rats
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The Effects of Temporary Inactivation of the Core and the Shell Subregions of the Nucleus Accumbens on Prepulse Inhibition of the Acoustic Startle Reflex and Activity in Rats

机译:伏隔核的核心和壳部分区域的暂时失活对大鼠惊吓反射和活动的脉冲抑制的影响。

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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 GABAA receptor agonist muscimol (0.5g/0.2l per side). The control group consisted of vehicle infused and unoperated rats. To ascertain the region selectivity of the infusions, 0.2l 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 72h 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.
机译:伏伏核可以分解成至少两个子区域:“核心”和“壳”。使用这些子区域的暂时化学灭活,我们研究了它们是否在听觉惊吓反射和活动的前脉冲抑制(PPI)的调节中有差异。为了这个目的,在大鼠的两侧都向其植入了针对核或壳的引导套管,并注入了GABAA受体激动剂麝香酚(每侧0.5g / 0.2l)。对照组由输注载体和未手术的大鼠组成。为了确定输注的区域选择性,将0.2l [3H]麝香酚注入另一组大鼠的核或壳中。行为结果表明,与对照组相比,核心的失活导致丧失了PPI的前脉冲强度依赖性。此外,与对照组相比,核心失活在输注后直接导致运动障碍,但此后24小时和72h引起运动亢进。在两个实验中,与对照相比,壳的失活都是无效的。放射自显影图的分析表明,药物向其他子区域的扩散极小,从而支持了灭活区域的选择性。这些结果进一步支持核和壳之间的功能解离,前者优先参与PPI和运动。将麝香酚注入核心后,持续的活动亢进可以用伏伏核中发生的补偿机制来解释。

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