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Plasticity-Related Activity in the Hippocampus, Anterior Cingulate, Orbitofrontal, and Prefrontal Cortex Following a Repeated Treatment with D2/D3 Agonist Quinpirole
H. Brozka, D. Alexova, D. Radostova, M. Janikova, B. Krajcovic, Š. Kubík, J. Svoboda, A. Stuchlik
Language English Country Switzerland
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NU20-04-00147
Agentura Pro Zdravotnický Výzkum České Republiky
NLK
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PubMed Central
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PubMed
33440912
DOI
10.3390/biom11010084
Knihovny.cz E-resources
- MeSH
- Dopamine D2 Receptor Antagonists pharmacology MeSH
- Quinpirole pharmacology MeSH
- Gyrus Cinguli drug effects physiology MeSH
- Hippocampus drug effects physiology MeSH
- Neurons drug effects metabolism MeSH
- Neuronal Plasticity drug effects physiology MeSH
- Genes, Immediate-Early MeSH
- Motor Activity drug effects MeSH
- Rats, Long-Evans MeSH
- Prefrontal Cortex drug effects physiology MeSH
- Receptors, Dopamine D2 metabolism MeSH
- Receptors, Dopamine D3 antagonists & inhibitors MeSH
- Gene Expression Regulation drug effects MeSH
- Stereotyped Behavior drug effects MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
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; n = 15) or saline (n = 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 Arc and Homer1a 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.
1st Faculty of Medicine Charles University 142 20 Prague Czech Republic
2nd Faculty of Medicine Charles University 142 20 Prague Czech Republic
3rd Faculty of Medicine Charles University 142 20 Prague Czech Republic
References provided by Crossref.org
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