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作 者:Ruizhe Nie Xinting Zhou Jiaru Fu Shanshan Hu Qilu Zhang Weikai Jiang Yizi Yan Xian Cao Danhua Yuan Yan Long Hao Hong Susu Tang
出 处:《Acta Pharmaceutica Sinica B》2024年第11期4789-4805,共17页药学学报(英文版)
基 金:National Natural Science Foundation of China(82373860 and 82071202 to Susu Tang,82173805 to Hao Hong);National Innovation and Entrepreneurship Training Program for Undergraduate(202410316198,China).
摘 要:Anxiety disorders are one of the most epidemic and chronic psychiatric disorders.An incom-plete understanding of anxiety pathophysiology has limited the development of highly effective drugs against these disorders.GPR17 has been shown to be involved in multiple sclerosis and some acute brain injury disorders.However,no study has investigated the role of GPR17 in psychiatric disorders.In a well-established chronic restraint stress(CRS)mouse model,using a combination of pharmacological and molecular biology techniques,viral tracing,in vitro electrophysiology recordings,in vivo fiber photom-etry,chemogenetic manipulations and behavioral tests,we demonstrated that CRS induced anxiety-like behaviors and increased the expression of GPR17 in basolateral amygdala(BLA)glutamatergic neurons.Inhibition of GPR17 by cangrelor or knockdown of GPR17 by adeno-associated virus in BLA glutama-tergic neurons effectively improved anxiety-like behaviors.Overexpression of GPR17 in BLA glutama-tergic neurons increased the susceptibility to anxiety-like behaviors.What's more,BLA glutamatergic neuronal activity was required for anxiolytic-like effects of GPR17 antagonist and GPR17 modulated anxiety-like behaviors via BLA to ventral hippocampal CAl glutamatergic projection.Our study finds for the first and highlights the new role of GPR17 in regulating anxiety-like behaviors and it might be a novel potential target for therapy of anxiety disorders.
关 键 词:GPR17 CRS Anxiety Basolateral amygdala VentralhippocampalCAl Glutamatergic neurons Glutamatergic projection CANGRELOR
分 类 号:R749.4[医药卫生—神经病学与精神病学]
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