Krištofiková Zdena, Vrajová Monika, Sírová Jana, Valeš Karel, Petrásek Tomáš, Schönig Kai, Tews Björn, Schwab Martin, Bartsch Dusan, Stuchlík Aleš, Rípová Daniela
Prague Psychiatric Centre , Prague , Czech Republic.
Front Behav Neurosci. 2013 Aug 12;7:90. doi: 10.3389/fnbeh.2013.00090. eCollection 2013.
It has been suggested that Nogo-A, a myelin-associated protein, could play a role in the pathogenesis of schizophrenia and that Nogo-A-deficient rodents could serve as an animal model for schizophrenic symptoms. Since changes in brain laterality are typical of schizophrenia, we investigated whether Nogo-A-deficient rats showed any signs of disturbed asymmetry in cortical N-methyl-d-aspartate (NMDA) receptor-nitric oxide synthase (NOS) pathway, which is reported as dysfunctional in schizophrenia. In particular, we measured separately in the right and left hemisphere of young and old Nogo-A-deficient male rats the expression of NMDA receptor subunits (NR1, NR2A, and NR2B in the frontal cortex) and activities of NOS isoforms [neuronal (nNOS), endothelial (eNOS), and inducible (iNOS) in the parietal cortex]. In young controls, we observed right/left asymmetry of iNOS activity and three positive correlations (between NR1 in the left and NR2B laterality, between NR2B in the right and left sides, and between NR1 in the right side and nNOS laterality). In old controls, we found bilateral decreases in NR1, an increase in NR2B in the right side, and two changes in correlations in the NR1-nNOS pathway. In young Nogo-A-deficient rats, we observed an increase in iNOS activity in the left hemisphere and two changes in correlations in NR1-nNOS and NR2A-eNOS, compared to young controls. Finally, we revealed in old Nogo-A-deficient animals, bilateral decreases in NR1 and one change in correlation between eNOS-iNOS, compared to old controls. Although some findings from schizophrenic brains did not manifest in Nogo-A-deficient rats (e.g., no alterations in NR2B), others did (e.g., alterations demonstrating accelerated aging in young but not old animals, those occurring exclusively in the right hemisphere in young and old animals and those suggesting abnormal frontoparietal cortical interactions in young animals).
有研究表明,髓鞘相关蛋白Nogo - A可能在精神分裂症的发病机制中起作用,并且Nogo - A基因缺陷的啮齿动物可作为精神分裂症症状的动物模型。由于大脑不对称性的改变是精神分裂症的典型特征,我们研究了Nogo - A基因缺陷的大鼠在皮质N - 甲基 - D - 天冬氨酸(NMDA)受体 - 一氧化氮合酶(NOS)通路中是否表现出任何不对称性紊乱的迹象,该通路在精神分裂症中被报道存在功能障碍。具体而言,我们分别测量了年轻和年老的Nogo - A基因缺陷雄性大鼠左右半球中NMDA受体亚基(额叶皮质中的NR1、NR2A和NR2B)的表达以及NOS同工型(顶叶皮质中的神经元型NOS、内皮型NOS和诱导型NOS)的活性。在年轻对照组中,我们观察到诱导型NOS活性的左右不对称性以及三个正相关关系(左侧的NR1与NR2B不对称性之间、右侧和左侧的NR2B之间以及右侧的NR1与神经元型NOS不对称性之间)。在年老对照组中,我们发现NR1的双侧减少、右侧NR2B的增加以及NR1 - 神经元型NOS通路中相关性的两个变化。与年轻对照组相比,在年轻的Nogo - A基因缺陷大鼠中,我们观察到左半球诱导型NOS活性增加以及NR1 - 神经元型NOS和NR2A - 内皮型NOS相关性的两个变化。最后,与年老对照组相比,我们在年老的Nogo - A基因缺陷动物中发现NR1的双侧减少以及内皮型NOS - 诱导型NOS之间相关性的一个变化。尽管精神分裂症大脑的一些发现未在Nogo - A基因缺陷大鼠中表现出来(例如,NR2B无改变),但其他一些发现则表现出来了(例如,在年轻但非年老动物中显示加速衰老的改变、在年轻和年老动物中仅发生在右半球的改变以及在年轻动物中提示额顶叶皮质异常相互作用的改变)。