Laboratory of the Neurophysiology of Memory, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 142 20 Prague, Czech Republic.
Second Faculty of Medicine, Charles University, 142 20 Prague, Czech Republic.
Biomolecules. 2021 Jan 11;11(1):84. doi: 10.3390/biom11010084.
Quinpirole (QNP) sensitization is a well-established model of stereotypical checking relevant to obsessive-compulsive disorder. Previously, we found that QNP-treated rats display deficits in hippocampus-dependent tasks. The present study explores the expression of immediate early genes (IEG) during QNP-induced stereotypical checking in the hippocampus, anterior cingulate cortex (ACC), orbitofrontal cortex (OFC), and medial prefrontal cortex (mPFC). Adult male rats were injected with QNP (0.5 mg/mL/kg; = 15) or saline ( = 14) daily for 10 days and exposed to an arena enriched with two objects. Visits to the objects and the corners of the arena were recorded. QNP-treated rats developed an idiosyncratic pattern of visits that persisted across experimental days. On day 11, rats were exposed to the arena twice for 5 min and sacrificed. The expression of IEGs and was determined using cellular compartment analysis of temporal activity by fluorescence in situ hybridization. IEG-positive nuclei were counted in the CA1 area of the hippocampus, ACC, OFC, and mPFC. We found significantly fewer IEG-positive nuclei in the CA1 in QNP-treated rats compared to controls. The overlap between IEG expressing neurons was comparable between the groups. We did not observe significant differences in IEG expression between QNP treated and control rats in ACC, OFC, and mPFC. In conclusion, treatment of rats with quinpirole decreases plasticity-related activity in the hippocampus during stereotypical checking.
喹吡罗(QNP)敏化是一种与强迫症相关的刻板检查的既定模型。先前,我们发现 QNP 处理的大鼠在海马体依赖的任务中表现出缺陷。本研究探讨了在 QNP 诱导的刻板检查过程中,海马体、前扣带皮层(ACC)、眶额皮层(OFC)和内侧前额叶皮层(mPFC)中即时早期基因(IEG)的表达。成年雄性大鼠每天接受 QNP(0.5mg/mL/kg;n=15)或生理盐水(n=14)注射 10 天,并暴露于富含两个物体的竞技场中。记录对物体和竞技场角落的访问次数。QNP 处理的大鼠表现出一种独特的访问模式,这种模式在实验期间持续存在。在第 11 天,大鼠两次暴露于竞技场 5 分钟并被处死。通过荧光原位杂交对细胞区室分析测定 IEG 和 的表达。在海马体 CA1 区、ACC、OFC 和 mPFC 中计数 IEG 阳性核。我们发现,与对照组相比,QNP 处理的大鼠 CA1 中的 IEG 阳性核显著减少。两组之间表达 IEG 的神经元的重叠是可比的。我们没有观察到 QNP 处理和对照组大鼠在 ACC、OFC 和 mPFC 之间 IEG 表达的显著差异。总之,喹吡罗治疗大鼠可减少刻板检查过程中海马体中与可塑性相关的活动。