Medicinal Chemistry and Drug Action, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville 3052, Victoria, Australia.
Brain Res. 2011 Mar 24;1381:52-65. doi: 10.1016/j.brainres.2011.01.017. Epub 2011 Jan 15.
Depriving weaned rats of social contact by rearing them in isolation brings about a spectrum of behavioural and neuropathological changes in adulthood which resemble some of the characteristics observed in schizophrenia. Hence, isolation rearing provides a non-pharmacological means to induce in an animal model certain aspects of schizophrenia with a neurodevelopmental origin. We compared the prepulse inhibition and locomotor activity behaviours in group-reared and isolation-reared rats in the context of determining the robustness of any behavioural changes following a subchronic parenteral drug administration protocol. The expression of synaptic, myelin and GABA-related proteins was also assessed in the brains of these rats using semi-quantitative fluorescence immunohistochemistry. Compared to their group-reared counterparts, isolation-reared rats displayed disruption in prepulse inhibition which was lost after repeated testing and subchronic vehicle administration. However, isolation-reared rats showed open-field hyperlocomotion post-subchronic vehicle treatment compared to group-reared rats. Isolation rearing resulted in reduced expression of synaptophysin, synapsin I, myelin basic protein and GABA(B1) receptor proteins, along with an increase in 2',3'-cyclic nucleotide 3'-phosphodiesterase. Of the brain areas examined these observed changes were localised to the hippocampal regions and the substantia nigra. These results suggest an alteration in the synaptic, myelin and GABA-related functions in the brains of isolation-reared rats that displayed behavioural anomalies. Since dysfunction in these systems has also been implicated in schizophrenia, our findings provide additional evidence to support the use of isolation rearing for schizophrenia research; however, its use in the screening of putative antipsychotics following subchronic administration needs to be undertaken warily.
将断奶大鼠隔离饲养以剥夺其社交接触,会导致其成年后出现一系列行为和神经病理学变化,这些变化类似于精神分裂症的一些特征。因此,隔离饲养为在动物模型中诱导具有神经发育起源的某些精神分裂症特征提供了一种非药理学手段。我们比较了群体饲养和隔离饲养大鼠的预脉冲抑制和运动活性行为,以确定亚慢性药物给药方案后任何行为变化的稳健性。还使用半定量荧光免疫组织化学评估了这些大鼠大脑中突触、髓鞘和 GABA 相关蛋白的表达。与群体饲养大鼠相比,隔离饲养大鼠的预脉冲抑制出现中断,经过反复测试和亚慢性载体给药后消失。然而,与群体饲养大鼠相比,隔离饲养大鼠在亚慢性载体处理后表现出开阔场过度活跃。与群体饲养大鼠相比,隔离饲养导致突触小体蛋白、突触素 I、髓鞘碱性蛋白和 GABA(B1)受体蛋白的表达减少,同时 2',3'-环核苷酸 3'-磷酸二酯酶增加。在所检查的大脑区域中,这些观察到的变化定位于海马区和黑质。这些结果表明,隔离饲养大鼠的大脑中突触、髓鞘和 GABA 相关功能发生改变,这些大鼠表现出行为异常。由于这些系统的功能障碍也与精神分裂症有关,我们的发现为支持使用隔离饲养进行精神分裂症研究提供了额外的证据;然而,在亚慢性给药后筛选潜在的抗精神病药物时,需要谨慎使用。