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Calcium imaging reveals depressive- and manic-phase-specific brain neural activity patterns in a murine model of bipolar disorder: a pilot study

Brain pathological features during manic/hypomanic and depressive episodes in the same patients with bipolar disorder (BPD) have not been described precisely. The study aimed to investigate depressive and manic-phase-specific brain neural activity patterns of BPD in the same murine model to provide...

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Published in:Translational psychiatry 2021-12, Vol.11 (1), p.619-619, Article 619
Main Authors: Chen, Min, Tian, Hongjun, Huang, Guoyong, Fang, Tao, Lin, Xiaodong, Shan, Jianmin, Cai, Ziyao, Chen, Gaungdong, Chen, Suling, Chen, Ce, Ping, Jing, Cheng, Langlang, Chen, Chunmian, Zhu, Jingjing, Zhao, Feifei, Jiang, Deguo, Liu, Chuanxin, Huang, Guangchuan, Lin, Chongguang, Zhuo, Chuanjun
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Language:English
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Summary:Brain pathological features during manic/hypomanic and depressive episodes in the same patients with bipolar disorder (BPD) have not been described precisely. The study aimed to investigate depressive and manic-phase-specific brain neural activity patterns of BPD in the same murine model to provide information guiding investigation of the mechanism of phase switching and tailored prevention and treatment for patients with BPD. In vivo two-photon imaging was used to observe brain activity alterations in the depressive and manic phases in the same murine model of BPD. Two-photon imaging showed significantly reduced Ca 2+ activity in temporal cortex pyramidal neurons in the depression phase in mice exposed to chronic unpredictable mild stress (CUMS), but not in the manic phase in mice exposed to CUMS and ketamine. Total integrated calcium values correlated significantly with immobility times. Brain Ca 2+ hypoactivity was observed in the depression and manic phases in the same mice exposed to CUMS and ketamine relative to naïve controls. The novel object recognition preference ratio correlated negatively with the immobility time in the depression phase and the total distance traveled in the manic phase. With recognition of its limitations, this study revealed brain neural activity impairment indicating that intrinsic emotional network disturbance is a mechanism of BPD and that brain neural activity is associated with cognitive impairment in the depressive and manic phases of this disorder. These findings are consistent with those from macro-imaging studies of patients with BPD. The observed correlation of brain neural activity with the severity of depressive, but not manic, symptoms need to be investigated further.
ISSN:2158-3188
2158-3188
DOI:10.1038/s41398-021-01750-8