Social defeat drives hyperexcitation of the piriform cortex to induce learning and memory impairment but not mood-related disorders in mice

• Published in: Translational psychiatry Vol. 12; no. 1; p. 380
• Main Authors: Wang, Hanjie, Li, Fang, Zheng, Xuefeng, Meng, Lianghui, Chen, Meiying, Hui, Yuqing, Li, Yifei, Xie, Keman, Zhang, Jifeng, Guo, Guoqing
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 10.09.2022; Nature Publishing Group
• Subjects: 14/19; 631/378; 64/60; 692/699/476/1414; 9/74; Alzheimer's disease; Behavior; Behavioral Sciences; Biological Psychology; Bullying; Laboratory animals; Medicine; Medicine & Public Health; Memory; Neurosciences; Pharmacotherapy; Psychiatry; Stress
• ISSN: 2158-3188; 2158-3188
• DOI: 10.1038/s41398-022-02151-1

Clinical studies have shown that social defeat is an important cause of mood-related disorders, accompanied by learning and memory impairment in humans. The mechanism of mood-related disorders has been widely studied. However, the specific neural network involved in learning and memory impairment caused by social defeat remains unclear. In this study, behavioral test results showed that the mice induced both learning and memory impairments and mood-related disorders after exposure to chronic social defeat stress (CSDS). c-Fos immunofluorescence and fiber photometry recording confirmed that CaMKIIα expressing neurons of the piriform cortex (PC) were selectively activated by exposure to CSDS. Next, chemogenetics and optogenetics were performed to activate PC CaMKIIα expressing neurons, which showed learning and memory impairment but not mood-related disorders. Furthermore, chemogenetic inhibition of PC CaMKIIα expressing neurons significantly alleviated learning and memory impairment induced by exposure to CSDS but did not relieve mood-related disorders. Therefore, our data suggest that the overactivation of PC CaMKIIα expressing neurons mediates CSDS-induced learning and memory impairment, but not mood-related disorders, and provides a potential therapeutic target for learning and memory impairment induced by social defeat.