基底外侧杏仁核
电针
抗抑郁药
焦虑
扁桃形结构
萧条(经济学)
神经病理性疼痛
慢性疼痛
神经科学
心理学
医学
针灸科
精神科
替代医学
病理
经济
宏观经济学
作者
Yiping Xie,Zui Shen,Xixiao Zhu,Yushuang Pan,Haiju Sun,Mengdi Xie,Qiuzhu Gong,Qunqi Hu,Jie Chen,Zemin Wu,Shuting Zhou,Boyu Liu,Xiaofen He,Boyi Liu,Xiaomei Shao,Jianqiao Fang
标识
DOI:10.1016/j.brainresbull.2024.111092
摘要
Chronic pain, such as neuropathic pain, can lead to anxiety, depression, and other negative emotions, thereby forming comorbidities and increasing the risk of chronic pain over time. Both the infralimbic amygdala (IL) and the basolateral amygdala (BLA) are significantly associated with negative emotions and pain, and they are known to have reciprocal connections. However, the role of IL-BLA circuit pathways in neuropathic pain-induced anxiety and depression remains unexplored. Electroacupuncture (EA) is frequently employed in the treatment of chronic pain and emotional disorders. However, The mechanism by which EA mediates its analgesic and emotion-alleviating effects via the IL-BLA circuit remains uncertain. Here, we used chemogenetic manipulation combined with behavioral tests to detect pain induced anxiety-like and depression-like behaviors. We observed that activation of the IL-BLA circuit by chemogenetic activation induced depression-like behavior of mice. Additionally, we discovered that chemogenetic activation of the IL-BLA circuit successfully prevented the beneficial effects of EA on depression-like behavior brought on by chronic pain in mice with spared nerve injury (SNI). We discovered that SNI-induced depression-like behavior could be mitigated by inhibiting the circuit, and EA had a comparable depressive-relieving effect. Furthermore, the IL-BLA circuit's activation or inhibition had no effect on the anxiety-like feelings brought on by SNI. Overall, our findings identify a specific neural circuit that selectively regulates pain-induced depression-like emotions, without affecting pain-induced anxiety-like emotions. This discovery offers a precise target for future treatments of comorbid pain and depression and provides a plausible explanation for the efficacy of EA in treating depression-like emotions associated with chronic pain.
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