前额叶皮质
神经科学
神经病理学
路易体
大脑皮层
皮质(解剖学)
认知
认知功能衰退
纤维
路易氏体型失智症
生物
帕金森病
痴呆
心理学
病理
医学
疾病
生物物理学
作者
Elena Espa,Erik Karl Håkan Clemensson,Kelvin C. Luk,Andreas Heuer,Tomas Björklund,M. Angela Cenci
摘要
Abstract Background Cortical α‐synuclein pathology plays a role in the development of cognitive dysfunction in both Parkinson's disease and dementia with Lewy bodies, although the causative cellular lesions have remained unclear. We aimed to address causal links between α‐synuclein‐driven pathology in the cerebral cortex and the development of cognitive impairments using new experimental models. Methods Neuronal overexpression of human α‐synuclein was induced in the rat medial prefrontal cortex using viral vectors. This was combined with inoculations of preformed fibrils of human α‐synuclein in some animals. Rats were evaluated with tests probing prefrontal cognitive functions (delayed matching/nonmatching to position and 5‐choice serial reaction time task). Patterns of neuropathology were characterized immunohistochemically. Results Neither α‐synuclein overexpression nor the fibril seeds alone yielded any behavioral phenotype. In contrast, combining the 2 approaches produced significant impairments in working memory, attention, and inhibitory control. All animals injected with α‐synuclein vectors exhibited high immunoreactivity for human α‐synuclein in the medial prefrontal cortex and its primary projection targets. However, only when this overexpression was combined with fibril inoculations did animals exhibit large, proteinase K‐resistant and Ser 129 ‐phosphorylated α‐synuclein intraneuronal inclusions in the medial prefrontal cortex and its closely interconnected brain regions. The inclusions were associated with distorted dendritic morphologies and partial neuronal loss in the targeted cortical areas. Conclusions Cortical overexpression of human α‐synuclein is not sufficient to produce cognitive dysfunction, whereas combining this overexpression with fibril seeds yields both cognitive and histopathological phenotypes that are relevant to human Lewy body disease. © 2019 International Parkinson and Movement Disorder Society
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