Chen Yang, Gu Yuhao, Wang Bianbian, Wei Anqi, Dong Nan, Jiang Yong, Liu Xiaoying, Zhu Li, Zhu Feng, Tan Tao, Jing Zexin, Mao Fenghan, Zhang Yichi, Yao Jingyu, Yang Yuxin, Wang Hongyan, Wu Hao, Li Hua, Zheng Chaowen, Duan Xueting, Huo Jingxiao, Wu Xuanang, Hu Shaoqin, Zhao Anran, Li Ziyang, Cheng Xu, Qin Yuhao, Song Qian, Zhan Shuqin, Qu Qiumin, Guan Fanglin, Xu Huadong, Kang Xinjiang, Wang Changhe
Department of Neurology, the Second Affiliated Hospital, Neuroscience Research Center, Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, 710049, China.
Department of Neurosurgery, the Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.
Nat Commun. 2024 Dec 4;15(1):10571. doi: 10.1038/s41467-024-54604-4.
Schizophrenia is a severe neuropsychiatric disease, but the initiation mechanisms are unclear. Although antipsychotics are effective against positive symptoms, therapeutic interventions for negative symptoms are limited due to the lack of pathophysiological mechanisms. Here we identify synaptotagmin-11 (Syt11) as a potential genetic risk factor and dopamine over-transmission as a mechanism in the development of schizophrenia. Syt11 expression is reduced in individuals with schizophrenia but restored following the treatment with antipsychotics. Syt11 deficiency in dopamine neurons in early adolescence, but not in adults, leads to persistent social deficits and other schizophrenia-like behaviors by mediating dopamine over-transmission in mice. Accordingly, dopamine neuron over-excitation before late adolescence induces persistent schizophrenia-associated behavioral deficits, along with the structural and functional alternations in the mPFC. Notably, local intervention of D2R with clinical drugs presynaptically or postsynaptically exhibits both acute and long-lasting therapeutic effects on social deficits in schizophrenia mice models. These findings not only define Syt11 as a risk factor and DA over-transmission as a potential risk factor initiating schizophrenia, but also propose two D2R-targeting strategies for the comprehensive and long-term recovery of schizophrenia-associated social withdrawal.
精神分裂症是一种严重的神经精神疾病,但其发病机制尚不清楚。尽管抗精神病药物对阳性症状有效,但由于缺乏病理生理机制,针对阴性症状的治疗干预有限。在此,我们确定突触结合蛋白-11(Syt11)为潜在的遗传风险因素,并确定多巴胺过度传递是精神分裂症发展过程中的一种机制。精神分裂症患者的Syt11表达降低,但在接受抗精神病药物治疗后可恢复。青春期早期而非成年期多巴胺神经元中的Syt11缺乏,通过介导小鼠体内多巴胺过度传递,导致持续的社交缺陷和其他类似精神分裂症的行为。因此,青春期晚期之前多巴胺神经元的过度兴奋会导致持续的精神分裂症相关行为缺陷,以及内侧前额叶皮质(mPFC)的结构和功能改变。值得注意的是,在突触前或突触后用临床药物对D2R进行局部干预,对精神分裂症小鼠模型的社交缺陷具有急性和长期的治疗效果。这些发现不仅将Syt11定义为一个风险因素,将多巴胺过度传递定义为引发精神分裂症的潜在风险因素,还提出了两种针对D2R的策略,以实现与精神分裂症相关的社交退缩的全面和长期恢复。