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甘草查尔酮 B 可通过调控 FoxO3/Wnt/β-连环蛋白通路改善创伤性脑损伤小鼠的神经功能障碍。

Licoricidin improves neurological dysfunction after traumatic brain injury in mice via regulating FoxO3/Wnt/β-catenin pathway.

机构信息

National Drug Clinical Trial Institution, Lanzhou University Second Hospital, Lanzhou, 730030, China.

The 5th Department of General Surgery, Lanzhou University Second Hospital, Lanzhou, 730030, China.

出版信息

J Nat Med. 2020 Sep;74(4):767-776. doi: 10.1007/s11418-020-01434-5. Epub 2020 Jul 12.

Abstract

Traumatic brain injury (TBI) is a major cause of death and disability around the world with no effective treatments currently. The present study was aimed to investigate the neuroprotective effect of licoricidin, one of the major components of licorice extract, on TBI mice and further explore the underlying mechanism. Male C57BL/6 mice were modeled by a modified weight-drop method to mimic TBI. All animals received treatment 30 min after TBI. The modified Neurological Severity Score (NSS) tests were performed at 2 h and 1-3 days after TBI. The brain edema was analyzed by dry-wet weight method. The malonaldehyde (MDA) levels and the activities of glutathione peroxidase (GSH-PX), superoxide dismutase (SOD) and catalase (CAT) were determined by Elisa. Apoptotic neurons were detected using terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) immunofluorescence and the expression of apoptotic proteins were measured by western blot. Activation of the FoxO3/Wnt/β-catenin was evaluated by western blot. The results showed that treatment with licoricidin could significantly decline the NSS scores and reduce the brain edema, hence promote the recovery of neurological function in TBI mice. It also elevated the phosphorylation of p66, brought down the levels of MDA, as well as antagonized the decrement in activities of GSH-PX, SOD and CAT induced by TBI. Moreover, licoricidin decreased the TUNEL positive neurons, downregulated the expression of Cyt-C, cleaved-Caspase-3, cleaved-Caspase-9 and Bax and upregulated the Bcl-2, attenuated cellular apoptosis. Licoricidin decreased the expression of FoxO3 and increased the Wnt/β-catenin in TBI mice. In conclusion, Licoricidin exerted neuroprotective effect on TBI model and the effect was possibly due to its antioxidative effect and antiapoptotic effect via regulating the FoxO3/Wnt/β-catenin pathway. Licoricidin may be a candidate drug for TBI therapy.

摘要

创伤性脑损伤(TBI)是全球范围内导致死亡和残疾的主要原因,但目前尚无有效的治疗方法。本研究旨在探讨甘草次酸(甘草提取物的主要成分之一)对 TBI 小鼠的神经保护作用,并进一步探讨其潜在机制。通过改良重物坠落法对雄性 C57BL/6 小鼠进行建模,以模拟 TBI。所有动物在 TBI 后 30 分钟接受治疗。在 TBI 后 2 小时和 1-3 天进行改良神经功能缺损评分(NSS)测试。采用干湿重法分析脑水肿。通过 ELISA 测定丙二醛(MDA)水平以及谷胱甘肽过氧化物酶(GSH-PX)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的活性。采用末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)免疫荧光法检测凋亡神经元,并通过 Western blot 测定凋亡蛋白的表达。通过 Western blot 评估 FoxO3/Wnt/β-catenin 的激活。结果表明,甘草次酸治疗可显著降低 NSS 评分,减轻脑水肿,从而促进 TBI 小鼠神经功能的恢复。它还能增加 p66 的磷酸化,降低 MDA 水平,并拮抗 TBI 引起的 GSH-PX、SOD 和 CAT 活性下降。此外,甘草次酸减少 TUNEL 阳性神经元,下调 Cyt-C、cleaved-Caspase-3、cleaved-Caspase-9 和 Bax 的表达,上调 Bcl-2,减轻细胞凋亡。甘草次酸降低 TBI 小鼠 FoxO3 的表达,增加 Wnt/β-catenin 的表达。综上所述,甘草次酸对 TBI 模型具有神经保护作用,其作用可能是通过调节 FoxO3/Wnt/β-catenin 通路发挥抗氧化和抗凋亡作用。甘草次酸可能是 TBI 治疗的候选药物。

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