基底外侧杏仁核
神经病理性疼痛
SNi公司
焦虑
心理学
痛觉超敏
慢性疼痛
高架加迷宫
医学
兴奋剂
扁桃形结构
神经科学
内科学
痛觉过敏
受体
伤害
精神科
化学
水解
生物化学
酸水解
作者
Mengwei Wu,Yeqing Chen,Zui Shen,Yichen Zhu,Siqi Xiao,Xia Zhu,Zemin Wu,Jing-Gen Liu,Chi Xu,Pingan Yao,Weiwei Xu,Yi Yang,Boyi Liu,Junying Du,Xiaofen He,Bo-Yu Liu,Xiaoming Jin,Jianqiao Fang,Xiaomei Shao
标识
DOI:10.1007/s12035-022-02911-6
摘要
Chronic pain, such as neuropathic pain, causes anxiety and other negative emotions, which aggravates the pain sensation and increases the risk of chronic pain over time. Dopamine receptor D1 (DRD1) and dopamine receptor D2 (DRD2) in the basolateral amygdala (BLA) have been implicated in mediating anxiety-related behaviors, but their potential roles in the BLA in neuropathic pain-induced anxiety have not been examined. Electroacupuncture (EA) is commonly used to treat chronic pain and emotional disorders, but it is still unclear whether EA plays a role in analgesia and anxiety relief through DRD1 and DRD2 in the BLA. Here, we used western blotting to examine the expression of DRD1 and DRD2 and pharmacological regulation combined with behavioral testing to detect anxiety-like behaviors. We observed that injection of the DRD1 antagonist SCH23390 or the DRD2 agonist quinpirole into the BLA contributed to anxiety-like behaviors in naive mice. EA also activated DRD1 or inhibited DRD2 in the BLA to alleviate anxiety-like behaviors. To further demonstrate the role of DRD1 and DRD2 in the BLA in spared nerve injury (SNI) model-induced anxiety-like behaviors, we injected the DRD1 agonist SKF38393 or the DRD2 antagonist sulpiride into the BLA. We found that both activation of DRD1 and inhibition of DRD2 could alleviate SNI-induced anxiety-like behaviors, and EA had a similar effect of alleviating anxiety. Additionally, neither DRD1 nor DRD2 in the BLA affected SNI-induced mechanical allodynia, but EA did. Overall, our work provides new insights into the mechanisms of neuropathic pain-induced anxiety and a possible explanation for the effect of EA treatment on anxiety caused by chronic pain.
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