二甲双胍
氧化应激
神经保护
炎症
嘌呤能受体
药理学
基因敲除
医学
过氧化氢
化学
受体
内分泌学
内科学
糖尿病
细胞凋亡
生物化学
作者
Gang Wang,Shurui Chen,Zhenya Shao,Yankun Li,Jiaqiang Wang,Liang Mao,Jian Li,Xifan Mei
标识
DOI:10.1139/cjpp-2020-0373
摘要
Metformin, the first medication that is often prescribed for the treatment of type 2 diabetes mellitus, was recently found to be neuroprotective. To study the mechanism underlying the neuroprotective effect of metformin, we pretreated primary spinal cord neurons with 50 µM or 100 µM metformin for 2 h prior to treatment with hydrogen peroxide (H2O2) for up to 48 h. Our results showed that H2O2 increased the expression of purinergic receptor P2X7 (P2X7R) in spinal cord neurons, which promoted the downstream pro-inflammatory cytokines release and oxidative stress. We found that metformin could reverse these pro-inflammatory and pro-oxidative effects of H2O2. Besides, P2X7R knockdown by siRNA suppressed H2O2-induced pro-inflammatory cytokine release and oxidative stress response. In conclusion, our results show that metformin can alleviate H2O2-induced inflammation and oxidative stress via modulating the P2X7R signaling pathway.
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