Petrasek Tomas, Prokopova Iva, Sladek Martin, Weissova Kamila, Vojtechova Iveta, Bahnik Stepan, Zemanova Anna, Schönig Kai, Berger Stefan, Tews Björn, Bartsch Dusan, Schwab Martin E, Sumova Alena, Stuchlik Ales
Department of Neurophysiology of Memory, Institute of Physiology, Academy of Sciences of the Czech Republic , Prague , Czech Republic ; First Faculty of Medicine, Charles University in Prague , Prague , Czech Republic.
Department of Neurophysiology of Memory, Institute of Physiology, Academy of Sciences of the Czech Republic , Prague , Czech Republic.
Front Behav Neurosci. 2014 Mar 18;8:90. doi: 10.3389/fnbeh.2014.00090. eCollection 2014.
Decreased levels of Nogo-A-dependent signaling have been shown to affect behavior and cognitive functions. In Nogo-A knockout and knockdown laboratory rodents, behavioral alterations were observed, possibly corresponding with human neuropsychiatric diseases of neurodevelopmental origin, particularly schizophrenia. This study offers further insight into behavioral manifestations of Nogo-A knockdown in laboratory rats, focusing on spatial and non-spatial cognition, anxiety levels, circadian rhythmicity, and activity patterns. Demonstrated is an impairment of cognitive functions and behavioral flexibility in a spatial active avoidance task, while non-spatial memory in a step-through avoidance task was spared. No signs of anhedonia, typical for schizophrenic patients, were observed in the animals. Some measures indicated lower anxiety levels in the Nogo-A-deficient group. Circadian rhythmicity in locomotor activity was preserved in the Nogo-A knockout rats and their circadian period (tau) did not differ from controls. However, daily activity patterns were slightly altered in the knockdown animals. We conclude that a reduction of Nogo-A levels induces changes in CNS development, manifested as subtle alterations in cognitive functions, emotionality, and activity patterns.
已表明Nogo-A依赖性信号水平降低会影响行为和认知功能。在Nogo-A基因敲除和敲低的实验啮齿动物中,观察到行为改变,这可能与神经发育起源的人类神经精神疾病,特别是精神分裂症相对应。本研究进一步深入了解实验大鼠中Nogo-A敲低的行为表现,重点关注空间和非空间认知、焦虑水平、昼夜节律性和活动模式。结果表明,在空间主动回避任务中认知功能和行为灵活性受损,而在穿梭箱回避任务中的非空间记忆则未受影响。在动物中未观察到精神分裂症患者典型的快感缺失迹象。一些测量表明Nogo-A缺陷组的焦虑水平较低。Nogo-A基因敲除大鼠的运动活动昼夜节律性得以保留,其昼夜周期(tau)与对照组无差异。然而,敲低动物的日常活动模式略有改变。我们得出结论,Nogo-A水平的降低会诱导中枢神经系统发育的变化,表现为认知功能、情绪和活动模式的细微改变。