Wu Yu-Jie, Ren Ke-Xing, Cai Kun-Yi, Zheng Chao, Xu Ai-Ping, Luo Hao, Wang Meng-Ya, Zhang Huan-Huan
Psychophysiology Laboratory, Wannan Medical College, Wuhu, Anhui 241002, China; Cell Electrophysiology Laboratory, Wannan Medical College, Wuhu, Anhui 241002, China.
Neurobiology Laboratory, Wannan Medical College, Wuhu, Anhui 241002, China.
Brain Res Bull. 2025 Jan;220:111185. doi: 10.1016/j.brainresbull.2024.111185. Epub 2024 Dec 29.
Post-traumatic stress disorder (PTSD) is characterized by anxiety, excessive fear, distress, and weakness as symptoms of a psychiatric disorder. However, the mechanism associated with its symptoms such as anxiety-like behaviors is not well understood. It is aimed to investigate the underlying mechanisms of the medial septum (MS)-medial habenula (MHb) neural circuit modulating the anxiety-like behaviors of PTSD mice through in vivo fiber photometry recording, optogenetics, behavioral testing by open-field and elevated plus maze, fluorescent gold retrograde tracer technology, and viral tracer technology. In the mouse PTSD model induced by compound stress consisting of single-prolonged stress combined with electrical foot shock, the average peak value of the Ca signals in both the MHb and MS glutamatergic neurons significantly increased. The anterograde and retrograde tracer markers were used to indicate the possible connection between MS and MHb via glutamatergic neural pathway. After the optogenetic manipulation of the MS-MHb pathway in mice with PTSD, if the MS-MHb glutamatergic pathway was inhibited, anxiety was relieved based on changes in the various indices of behavioral experiments in mice with PTSD. Moreover, the heart rate of mice decreased. In conclusion, both glutamatergic neurons located in MS and MHb can be engaged in the development of PTSD anxiety-like behavior, and the MS-MHb can be related to the regulation of PTSD anxiety-like behavior and cardiac function through the glutamatergic neural pathway.
创伤后应激障碍(PTSD)的特征是焦虑、过度恐惧、痛苦和虚弱,这些都是精神障碍的症状。然而,与焦虑样行为等症状相关的机制尚未完全了解。本研究旨在通过体内光纤光度记录、光遗传学、旷场和高架十字迷宫行为测试、荧光金逆行示踪技术和病毒示踪技术,研究内侧隔核(MS)-内侧缰核(MHb)神经回路调节PTSD小鼠焦虑样行为的潜在机制。在由单次长时间应激与电击足底组成的复合应激诱导的小鼠PTSD模型中,MHb和MS谷氨酸能神经元中Ca信号的平均峰值均显著增加。顺行和逆行示踪标记用于表明MS和MHb之间可能通过谷氨酸能神经通路建立联系。对PTSD小鼠的MS-MHb通路进行光遗传学操作后,如果MS-MHb谷氨酸能通路受到抑制,根据PTSD小鼠行为实验的各项指标变化,焦虑症状得到缓解。此外,小鼠的心率下降。总之,位于MS和MHb的谷氨酸能神经元都可能参与PTSD焦虑样行为的发生发展,并且MS-MHb可能通过谷氨酸能神经通路与PTSD焦虑样行为和心脏功能的调节有关。