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预处理用山奈酚通过抑制 MAPKs-NF-κB 信号通路和继发性脊髓损伤后的细胞焦亡来减轻小胶质细胞介导的神经炎症。

Pretreatment with kaempferol attenuates microglia-mediate neuroinflammation by inhibiting MAPKs-NF-κB signaling pathway and pyroptosis after secondary spinal cord injury.

机构信息

Division of Spine Surgery, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.

Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.

出版信息

Free Radic Biol Med. 2021 May 20;168:142-154. doi: 10.1016/j.freeradbiomed.2021.03.037. Epub 2021 Apr 3.

Abstract

Spinal cord injury (SCI) is a devastating injury that characterized by oxidative stress and inflammatory response. Kaempferol is reported to be an anti-neuroinflammation in neurologic disorders. Nevertheless, the role and mechanism of kaempferol in SCI remains unclear. The present study aims to investigate effects of kaempferol on SCI and its possible underlying mechanisms in in vivo and in vitro models. A C5 hemi-contusion injury was induced in Sprague-Dawley rats to investigate the neuroprotective effects of kaempferol after SCI. For in vitro study, the BV2 microglia cell lines were pretreated with or without kaempferol. A combination of molecular and histological methods was used to clarify the mechanism and explore the signaling pathway both in vivo and in vitro. One-way analysis of variance (ANOVA) was conducted with Bonferroni post hoc tests to examine the differences between groups. The in vivo studies showed that kaempferol could improve the recovery of hindlimb motor function and ameliorate tissue damage in the spinal cord after SCI. Moreover, administration of kaempferol reduced microglia activation and oxidative stress level in the spinal cord. The in vitro studies showed that kaempferol suppressed the microglia activation resulting from the administration of LPS with ATP to BV-2 cells. Pretreated BV2 cells with kaempferol reduced the generation of reactive oxygen species (ROS) by inhibiting NADPH oxidase 4, and then, suppressed the phosphorylation of p38 MAPK and JNK, which subsequently inhibited nuclear translocation of NF-κB p65 to express pro-inflammatory factors. We also observed that kaempferol could inhibite the pyroptosis related proteins (NLRP3 Caspase-1 p10 ASC N-GSDMD) and reduce the release of IL-18 and IL-1β. In conclusion, kaempferol was able to reduce oxidative stress and inflammatory response through down-regulation of ROS dependent MAPKs- NF-κB and pyroptosis signaling pathway, which suggested that kaempferol might be a novel promising therapeutic agent for SCI.

摘要

脊髓损伤(SCI)是一种破坏性损伤,其特征是氧化应激和炎症反应。山奈酚据报道在神经疾病中具有抗神经炎症作用。然而,山奈酚在 SCI 中的作用和机制尚不清楚。本研究旨在探讨山奈酚在体内和体外模型中对 SCI 的影响及其可能的潜在机制。在 Sprague-Dawley 大鼠中诱导 C5 半挫伤损伤,以研究 SCI 后山奈酚的神经保护作用。在体外研究中,用或不用山奈酚预处理 BV2 小胶质细胞系。采用分子和组织学方法相结合,在体内和体外阐明其作用机制和探讨信号通路。采用单因素方差分析(ANOVA),并用 Bonferroni 事后检验比较组间差异。体内研究表明,山奈酚可改善 SCI 后后肢运动功能的恢复,并改善脊髓组织损伤。此外,山奈酚给药可降低脊髓中小胶质细胞的激活和氧化应激水平。体外研究表明,山奈酚可抑制 LPS 和 ATP 处理 BV-2 细胞引起的小胶质细胞激活。用山奈酚预处理 BV2 细胞可通过抑制 NADPH 氧化酶 4 减少活性氧(ROS)的产生,进而抑制 p38 MAPK 和 JNK 的磷酸化,从而抑制 NF-κB p65 的核转位以表达促炎因子。我们还观察到,山奈酚可抑制焦亡相关蛋白(NLRP3 Caspase-1 p10 ASC N-GSDMD)并减少 IL-18 和 IL-1β 的释放。总之,山奈酚通过下调 ROS 依赖性 MAPKs-NF-κB 和焦亡信号通路,减轻氧化应激和炎症反应,表明山奈酚可能是 SCI 的一种有前途的新型治疗药物。

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