神经炎症
小胶质细胞
七氟醚
海马结构
医学
炎症
下调和上调
神经认知
内科学
免疫学
药理学
化学
认知
精神科
生物化学
基因
作者
Chunchun Tang,Xue Zheng,Yuanping Zhong,Dongqin Chen,Yuhang Zhu,Sihui Wang,Lei Xiong,Zhijun Zhu
标识
DOI:10.1016/j.jneuroim.2023.578070
摘要
Microglia-mediated neuroinflammatory responses play a key role in perioperative neurocognitive disorders (PND). Triggering receptor expressed on myeloid cells-1 (TREM1) has been shown to be a key regulator of inflammation. However, its role in PND remains largely unknown. This study aimed to evaluate the role of TREM1 in sevoflurane-induced PND. We applied AAV knockdown TREM1 in hippocampal microglia in aging mice. The mice were then subjected to neurobehavioral and biochemical testing after the intervention of sevoflurane. We found that sevoflurane inhalation can cause PND in mice, increase hippocampal TREM1 expression, polarize microglia to M1 type, upregulate TNF-α and IL-1β expression (pro-inflammatory), and inhibit TGF-β and IL-10 expression (anti-inflammatory). Knocking down TREM1 can improve sevoflurane-induced cognitive dysfunction, reduce M1 type marker iNOS, and increase M2 type marker ARG, improving the neuroinflammation. TREM1 is a target for sevoflurane-induced PND prevention.
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