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Neurobiol Dis ; 199: 106584, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-38945496

RESUMO

The temporal component of episodic memory has been recognized as a sensitive behavioral marker in early stage of Alzheimer's disease (AD) patients. However, parallel studies in AD animals are currently lacking, and the underlying neural circuit mechanisms remain poorly understood. Using a novel AppNL-G-F knock-in (APP-KI) rat model, the developmental changes of temporal order memory (TOM) and the relationship with medial prefrontal cortex and perirhinal cortex (mPFC-PRH) circuit were determined through in vivo electrophysiology and microimaging technique. We observed a deficit in TOM performance during the object temporal order memory task (OTOMT) in APP-KI rats at 6 month old, which was not evident at 3 or 4 months of age. Alongside behavioral changes, we identified a gradually extensive and aggravated regional activation and functional alterations in the mPFC and PRH during the performance of OTOMT, which occurred prior to the onset of TOM deficits. Moreover, coherence analysis showed that the functional connectivity between the mPFC and PRH could predict the extent of future behavioral performance. Further analysis revealed that the aberrant mPFC-PRH interaction mainly attributed to the progressive deterioration of synaptic transmission, information flow and network coordination from mPFC to PRH, suggesting the mPFC dysfunction maybe the key area of origin underlying the early changes of TOM. These findings identify a pivotal role of the mPFC-PRH circuit in mediating the TOM deficits in the early stage of AD, which holds promising clinical translational value and offers potential early biological markers for predicting AD memory progression.


Assuntos
Doença de Alzheimer , Córtex Perirrinal , Córtex Pré-Frontal , Animais , Córtex Pré-Frontal/fisiopatologia , Córtex Perirrinal/fisiologia , Doença de Alzheimer/fisiopatologia , Ratos , Masculino , Transtornos da Memória/fisiopatologia , Modelos Animais de Doenças , Ratos Transgênicos , Vias Neurais/fisiopatologia , Memória Episódica
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