Department of Neurosurgery, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Brain Res Bull. 2019 Mar;146:320-326. doi: 10.1016/j.brainresbull.2019.01.027. Epub 2019 Feb 1.
Nucleotide oligomerization domain(NOD)-like receptor protein-3(NLRP3) inflammasome is a multiprotein complex, which results in the inflammatory response in early brain injury(EBI) after subarachnoid hemorrhage(SAH). MCC950, a specific NLRP3 inhibitor, plays neuroprotective effects in several central nervous system diseases. However, the role of MCC950 in SAH remains elusive. This study aims to investigate whether MCC950 exerts neuroprotection after experimental SAH and further explore the potential mechanisms. The SAH model was induced by endovascular perforation process using adult male Sprague-Dawley rats. MCC950 was injected intraperitoneally 1 h after SAH with a dose of 10 mg/kg. The results showed that MCC950 significantly ameliorated severe brain edema and neurological dysfunction. Furthermore, MCC950 efficiently reduced NLRP3 inflammasome expression as well as the pro-inflammatory cytokines, such as TNF-α, IL-1ß, and IL-6. In addition, the protective effect of MCC950 was blunted by lipopolysaccharide. In conclusion, our findings suggest that MCC950 alleviated SAH-induced EBI by suppressing inflammation.
核苷酸寡聚化结构域(NOD)样受体蛋白 3(NLRP3)炎性小体是一种多蛋白复合物,可导致蛛网膜下腔出血(SAH)后的早期脑损伤(EBI)发生炎症反应。MCC950 是一种特异性 NLRP3 抑制剂,在几种中枢神经系统疾病中具有神经保护作用。然而,MCC950 在 SAH 中的作用仍不清楚。本研究旨在探讨 MCC950 在实验性 SAH 后是否具有神经保护作用,并进一步探讨其潜在机制。通过成年雄性 Sprague-Dawley 大鼠的血管内穿孔过程诱导 SAH 模型。在 SAH 后 1 小时通过腹腔内注射以 10mg/kg 的剂量给予 MCC950。结果表明,MCC950 显著改善了严重的脑水肿和神经功能障碍。此外,MCC950 还能有效降低 NLRP3 炎性小体的表达以及促炎细胞因子 TNF-α、IL-1β 和 IL-6。此外,脂多糖削弱了 MCC950 的保护作用。总之,我们的研究结果表明,MCC950 通过抑制炎症缓解了 SAH 诱导的 EBI。