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慢性神经病理性疼痛诱导的类似抑郁而非焦虑样行为与下丘脑扣带回-基底外侧杏仁核环路的关系及电针对其的抗抑郁作用。

Infralimbic-basolateral amygdala circuit associated with depression-like not anxiety-like behaviors induced by chronic neuropathic pain and the antidepressant effects of electroacupuncture.

机构信息

Key Laboratory of Acupuncture and Neurology of Zhejiang Province, Department of Neurobiology and Acupuncture Research, the Third Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.

Department of Acupuncture and Moxibustion, the First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Brain Res Bull. 2024 Nov;218:111092. doi: 10.1016/j.brainresbull.2024.111092. Epub 2024 Oct 5.

Abstract

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.

摘要

慢性疼痛,如神经病理性疼痛,可导致焦虑、抑郁和其他负面情绪,从而形成共病,并随着时间的推移增加慢性疼痛的风险。边缘下脑区(IL)和基底外侧杏仁核(BLA)都与负面情绪和疼痛密切相关,它们之间存在相互联系。然而,IL-BLA 回路在神经病理性疼痛引起的焦虑和抑郁中的作用尚不清楚。电针(EA)常用于治疗慢性疼痛和情绪障碍。然而,EA 通过 IL-BLA 回路介导其镇痛和缓解情绪作用的机制尚不清楚。在这里,我们使用化学遗传操作结合行为测试来检测疼痛引起的焦虑样和抑郁样行为。我们观察到化学遗传激活 IL-BLA 回路会引起小鼠的抑郁样行为。此外,我们发现化学遗传激活 IL-BLA 回路成功地阻止了 EA 对 spared nerve injury(SNI)小鼠慢性疼痛引起的抑郁样行为的有益作用。我们发现 SNI 诱导的抑郁样行为可以通过抑制回路来缓解,而 EA 具有类似的抗抑郁作用。此外,IL-BLA 回路的激活或抑制对 SNI 引起的焦虑样感觉没有影响。总的来说,我们的发现确定了一个特定的神经回路,它选择性地调节疼痛引起的抑郁样情绪,而不影响疼痛引起的焦虑样情绪。这一发现为治疗疼痛和抑郁共病提供了一个精确的靶点,并为 EA 治疗与慢性疼痛相关的抑郁样情绪的疗效提供了一个合理的解释。

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