Wang Wang, Liu Weizhen, Liu Sufang, Duan Dongxiao, Ma Yajing, Zhang Zijuan, Li Changsheng, Tang Yuanyuan, Wang Zhiju, Xing Ying
Department of Physiology and Neurobiology, School of Basic Medical Sciences, Zhengzhou University, No.100 Science Road, Gao-Xin District, Henan, 450001, Zhengzhou, China.
The Academy of Medical Sciences of Zhengzhou University, Henan, 450001, Zhengzhou, China.
Mol Neurobiol. 2025 Mar;62(3):2817-2834. doi: 10.1007/s12035-024-04444-6. Epub 2024 Aug 23.
Postoperative pain is a type of pain that occurs in clinical patients after surgery. Among the factors influencing the transition from acute postoperative pain to chronic postoperative pain, chronic stress has received much attention in recent years. Here, we investigated the role of dopamine receptor D1/D2 expressing pyramidal neurons in the prelimbic cortex (PrL) in modulating chronic social defeat stress (CSDS)-induced anxiety-like behavior comorbidity with postoperative hyperalgesia in male mice. Our results showed that preoperative CSDS induced anxiety-like behavior and significantly prolonged postoperative pain caused by plantar incision, but did not affect plantar wound recovery and inflammation. Reduced activation of dopamine receptor D1 or D2 expressing neurons in the PrL is a remarkable feature of male mice after CSDS, and chronic inhibition of dopamine receptor D1 or D2 expressing neurons in the PrL induced anxiety-like behavior and persistent postoperative pain. Further studies found that activation of D1 expressing but not D2 expressing neurons in the PrL ameliorated CSDS-induced anxiety-like behavior and postoperative hyperalgesia. Our results suggest that dopamine receptor D1 expressing neurons in the PrL play a crucial role in CSDS-induced anxiety-like behavior comorbidity with postoperative hyperalgesia in male mice.
术后疼痛是临床患者术后出现的一种疼痛类型。在影响术后急性疼痛向慢性术后疼痛转变的因素中,慢性应激近年来受到了广泛关注。在此,我们研究了前额叶皮质(PrL)中表达多巴胺受体D1/D2的锥体神经元在调节慢性社会挫败应激(CSDS)诱导的雄性小鼠焦虑样行为合并术后痛觉过敏中的作用。我们的结果表明,术前CSDS诱导了焦虑样行为,并显著延长了足底切口引起的术后疼痛,但不影响足底伤口愈合和炎症。CSDS后雄性小鼠的一个显著特征是PrL中表达多巴胺受体D1或D2的神经元激活减少,并且对PrL中表达多巴胺受体D1或D2的神经元进行慢性抑制会诱导焦虑样行为和持续性术后疼痛。进一步的研究发现,激活PrL中表达D1而非D2的神经元可改善CSDS诱导的焦虑样行为和术后痛觉过敏。我们的结果表明,PrL中表达多巴胺受体D1的神经元在CSDS诱导的雄性小鼠焦虑样行为合并术后痛觉过敏中起关键作用。