自闭症
神经科学
心理学
焦虑
纹状体
边缘下皮质
光遗传学
腹侧纹状体
前额叶皮质
发展心理学
精神科
认知
多巴胺
作者
Yifan Luo,Lu Lu,Heng‐Yi Song,Xu Han,Zhi-Wei Zheng,Zhouyue Wu,Chen-Chen Jiang,Chu Tong,Hao-Yang Yuan,Xiuxiu Liu,Xiang Chen,Meiling Sun,Yang Tang,Heng‐Yu Fan,Feng Han,Yuanqing Lu
标识
DOI:10.1038/s41380-023-01954-y
摘要
Abstract The comorbidity of autism spectrum disorder and anxiety is common, but the underlying circuitry is poorly understood. Here, Tmem74 -/- mice showed autism- and anxiety-like behaviors along with increased excitability of pyramidal neurons (PNs) in the prelimbic cortex (PL), which were reversed by Tmem74 re-expression and chemogenetic inhibition in PNs of the PL. To determine the underlying circuitry, we performed conditional deletion of Tmem74 in the PNs of PL of mice, and we found that alterations in the PL projections to fast-spiking interneurons (FSIs) in the dorsal striatum (dSTR) (PL PNs –dSTR FSIs ) mediated the hyperexcitability of FSIs and autism-like behaviors and that alterations in the PL projections to the PNs of the basolateral amygdaloid nucleus (BLA) (PL PNs –BLA PNs ) mediated the hyperexcitability of PNs and anxiety-like behaviors. However, the two populations of PNs in the PL had different spatial locations, optogenetic manipulations revealed that alterations in the activity in the PL–dSTR or PL–BLA circuits led to autism- or anxiety-like behaviors, respectively. Collectively, these findings highlight that the hyperactivity of the two populations of PNs in the PL mediates autism and anxiety comorbidity through the PL–dSTR and PL–BLA circuits, which may lead to the development of new therapeutics for the autism and anxiety comorbidity.
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