紫铆因通过激活SIRT1介导FOXO1/NF-κB信号通路改善坐骨神经损伤
车敏, 张辉沈阳医学院附属中心医院手外一科, 沈阳 110024
收稿日期:
2023-05-08出版日期:
2024-02-28发布日期:
2024-01-12通讯作者:
张辉E-mail:59526543@qq.com作者简介:
车敏(1982-),男,副教授,博士.基金资助:
国家自然科学基金(8197080581);辽宁省自然科学基金(2020-MS-146);辽宁省高校基本科研项目(LJKMZ20221781)关键词: 紫铆因, 坐骨神经损伤, 沉默信息调节因子2相关酶1, FOXO1/NF-κB信号通路
Abstract: Objective This study aimed to explore the effect and possible mechanism of SIRT1 activation induced by butein on sciatic nerve injury in rats. Methods A total of 30 rats were randomly divided into a sham operation group, a sciatic nerve injury group, and a butein group, with 10 rats in each group. BBB motor scores and sciatic nerve function index were detected on the modeling surgery day, the 7th day after surgery, and the 14th day after surgery. The pathological changes of the sciatic nerve in each group were observed by HE staining. The apoptosis of sciatic nerve cells in each group was detected by TdT-mediated dUTP nick end labeling (TUNEL). The expression of BDNF, MBP, GAP-43, SIRT1, FOXO1, Keap1, and NF-κB in the sciatic nerve was detected by Western blotting. Results Butein improved the pathological injury of the sciatic nerve, reduced the apoptosis of sciatic nerve cells, increased BDNF, MBP, GAP-43, and SIRT1 expression, and decreased FOXO1, Keap1, and NF-κB expression in the sciatic nerve. Conclusion Butein can inhibit FOXO1/NF-κB signaling pathway activation by up-regulating SIRT1 expression in rats with sciatic nerve injury and then improve the sciatic nerve pathological injury in rats.
Key words: butein, sciatic nerve injury, SIRT1, FOXO1/NF-κB signaling pathway
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