Journal
PHARMACOLOGICAL RESEARCH
Volume 163, Issue -, Pages -Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2020.105355
Keywords
Kctd12; Depression; GABA(B)R antagonists; Fluoxetine; Dentate gyms; Neuronal excitability
Categories
Funding
- Foundation for Innovative Research Groups of NSFC [81721005]
- National Natural Science Foundation of China [81971266, 81671438, 81673414]
- PCSIRT [IRT13016]
- Program for HUST Academic Frontier Youth Team [2017QYTD17]
- Integrated Innovative Team for Major Human Diseases Program of Tongji Medical College, HUST
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This study identified that Kctd12 in the DG plays a critical role in regulating stress responses, making it a promising therapeutic target for stress-related psychiatric disorders, including depression.
Adaptive responses to stress are critical to enhance physical and mental well-being, but excessive or prolonged stress may cause inadaptability and increase the risks of psychiatric disorders, such as depression. GABA(B)R signaling is fundamental to brain function and has been identified in neuropsychiatric disorders. KCTD12 is a critical auxiliary subunit in GABA(B)R signaling, but its role in mental disorders, such as depression is unclear. In the present study, we used a well-validated mice model, chronic social defeat stress (CSDS) to investigate behavioral responses to stress and explore the role of Kctd12 in stress response, as well as the relevant mechanisms. We found that CSDS increased the expression of Kctd12 in the dentate gyms (DG), a subregion of hippocampus. Overexpression of Kctd12 in DG induced higher responsiveness to acute stress and increased vulnerability to social stress in mice, whereas knock-down of Kctd12 in DG prevented the social avoidance. Furthermore, an increased expression of GABA(B) receptor 2 (GB2) in the DG of CSDS-treated mice was observed, and CGP35348, an antagonist of GABA(B)R, improved the stress-induced behavior responses along with suppressing the excess expression of Kctd12. In addition, Kctd12 regulated the excitability of granule cell in DG, and the stimulation of neuronal activity by silencing Kctdl 2 contributed to the antidepressant-like effect of fluoxe-tine. These findings identify that the Kctd12 in DG works as a critical mediator of stress responses, providing a promising therapeutic target in stress-related psychiatric disorders, including depression.
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