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Brain Microglial Activation in Chronic Pain-Associated Affective Disorder

机译:慢性疼痛相关情感障碍中的脑小胶质细胞活化。

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A growing body of evidence from both clinical and animal studies indicates that chronic neuropathic pain is associated with comorbid affective disorders. Spinal cord microglial activation is involved in nerve injury-induced pain hypersensitivity characterizing neuropathic pain. However, thorough assessments of microglial activation in the brain after nerve injury are lacking. In the present study, we characterized microglial activation in brain sub-regions of CX3CR1GFP/+ mice after chronic constriction injury (CCI) of the sciatic nerve, including observations at delayed time points when affective brain dysfunction such as depressive-like behaviors typically develop. Mice manifested chronic mechanical hypersensitivity immediately after CCI and developed depressive-like behaviors 8 weeks post-injury. Concurrently, significant increases of soma size and microglial cell number were observed in the medial prefrontal cortex (mPFC), hippocampus, and amygdala 8 weeks post-injury. Transcripts of CD11b, and TNF-α, genes associated with microglial activation or depressive-like behaviors, are correspondingly upregulated in these brain areas. Our results demonstrate that microglia are activated in specific brain sub-regions after CCI at delayed time points and imply that brain microglial activation plays a role in chronic pain-associated affective disorders.
机译:来自临床和动物研究的越来越多的证据表明,慢性神经性疼痛与合并症情感障碍有关。脊髓小胶质细胞活化涉及神经损伤引起的疼痛超敏反应,表征神经性疼痛。但是,缺乏对神经损伤后大脑中小胶质细胞激活的全面评估。在本研究中,我们表征了坐骨神经慢性压迫性损伤(CCI)后CX3CR1GFP / +小鼠大脑亚区域的小胶质细胞活化,包括在典型的抑郁性行为等情感性脑功能障碍发展的延迟时间观察。小鼠在CCI后立即表现出慢性机械性超敏反应,并且在受伤后8周出现了类似抑郁的行为。同时,受伤后8周,在内侧前额叶皮层(mPFC),海马和杏仁核中观察到躯体大小和小胶质细胞数量显着增加。与这些小胶质细胞激活或抑郁样行为有关的基因CD11b和TNF-α的转录本在这些脑区中相应上调。我们的结果表明,小胶质细胞在CCI后特定的脑子区域在延迟的时间点被激活,并且暗示脑小胶质细胞的激活在慢性疼痛相关的情感障碍中起作用。

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