已发表论文

艾氯胺酮对抑郁症的影响:通过激活 BDNF/TrkB/PI3K/AKT 通路靶向氧化应激和神经元凋亡

 

Authors Zhang Y, Cai Q, Wang L, Zhang B

Received 21 October 2024

Accepted for publication 30 July 2025

Published 25 August 2025 Volume 2025:21 Pages 1783—1793

DOI https://doi.org/10.2147/NDT.S502090

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr Jun Chen

Yueyi Zhang,1,* Qianqian Cai,2,* Lingshan Wang,3 Bei Zhang4 

1Tianjin Medical College Pharmacy and Biotechnology Department, Tianjin, People’s Republic of China; 2The Rehabilitation Center of Tianjin Hospital in Tianjin, Tianjin, People’s Republic of China; 3Department of Human Resources, Tianjin Medical University General Hospital Airport Hospital, Tianjin, People’s Republic of China; 4Department of Pharmacy, Tianjin First Central Hospital, Tianjin, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Yueyi Zhang, Pharmacy and Biotechnology Department, Tianjin Medical College, No. 1, Chenglindao Dongjuzi, Dongli District, Tianjin, People’s Republic of China, Email zhangyueran93@163.com

Background & Aims: Esketamine, a promising treatment for treatment-resistant depression, has shown potential advantages over traditional antidepressants. However, its mechanisms remain unclear. This study explores how esketamine alleviates depressive behaviors through activation of the BDNF/TrkB/PI3K/AKT signaling pathway.
Methods: Using a Chronic Unpredictable Mild Stress (CUMS) rat model, behavioral assays (Sucrose Preference Test, Morris Water Maze Test) and histological analyses (HE and Nissl’s staining) were performed. Esketamine (5 mg/kg) treatment was administered to evaluate its antidepressant effects, and the PI3K inhibitor, PI3K-IN-6, was used to investigate the role of the PI3K/AKT pathway in the underlying mechanism.
Results: Esketamine treatment improved depressive behaviors, enhanced neuronal structure, and reduced apoptosis and oxidative stress. These effects were linked to the activation of the BDNF/TrkB/PI3K/AKT pathway. PI3K-IN-6 reversed the effects, confirming the pathway’s involvement.
Conclusion: Esketamine alleviates depressive behaviors by activating the BDNF/TrkB/PI3K/AKT signaling pathway, reducing oxidative stress and inhibiting neuronal apoptosis. These findings highlight the therapeutic potential of esketamine in treating depression, particularly in cases where traditional treatments fail.

Keywords: esketamine, BDNF/TrkB/PI3K/AKT, CUMS rats, depression, oxidative stress