• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人参皂苷 Rg1 通过 Nrf2/HO-1 信号通路抑制脊髓损伤大鼠的氧化应激和炎症。

Ginsenoside Rg1 inhibits oxidative stress and inflammation in rats with spinal cord injury via Nrf2/HO-1 signaling pathway.

机构信息

Department of Orthopedics.

Anesthesiology.

出版信息

Neuroreport. 2022 Jan 19;33(2):81-89. doi: 10.1097/WNR.0000000000001757.

DOI:10.1097/WNR.0000000000001757
PMID:34954769
Abstract

OBJECTIVES

In this study, our objective was to investigate the underlying mechanism of the neuroprotective role of ginsenoside Rg1 in attenuating spinal cord injury (SCI).

METHODS

A rat SCI model was established and treated with ginsenoside Rg1 and nuclear factor erythroid 2-related factor2(Nrf2) inhibitor all-trans retinoic acid (ATRA). The protective effects of ginsenoside Rg1 were evaluated by Basso, Beattie and Bresnahan (BBB) scale, hematoxylin/eosin staining, ELISA assay, western blotting and quantitative reverse transcription PCR (RT-qPCR).

RESULTS

Ginsenoside Rg1 alleviated neuronal edema and bleeding in the injured spinal cord, reduced inflammatory cell infiltration and cell necrosis, further repaired the injured spinal cord structure, improved BBB motor score in the SCI rat model and improved hind limb motor function. Meanwhile, ginsenoside Rg1 significantly increased the content of antioxidant enzymes superoxide dismutase and glutathione, and inhibited the production of oxidative marker malondialdehyde. In addition, ginsenoside Rg1also significantly inhibits the activities of the inflammatory factors tumor necrosis factor-α, interleukin-1β (IL-1β) and interleukin-6 (IL-6) to reduce the inflammatory response after trauma. Furthermore, western blot and RT-qPCR also suggested that ginsenoside Rg1 could activate the protein expression of Nrf2 and heme oxygenase-1 (HO-1) after SCI, and the inhibition of ATRA on these improvements further verified the neuroprotective effect of Nrf2 and HO-1 in ginsenoside Rg1 on SCI.

CONCLUSION

Ginsenoside Rg1 has a neuroprotective effect on SCI and can improve motor dysfunction caused by injury. The underlying mechanism may play antioxidative stress and anti-inflammatory effect by regulating the Nrf2/HO-1 signaling pathway.

摘要

目的

本研究旨在探讨人参皂苷 Rg1 减轻脊髓损伤(SCI)的神经保护作用的潜在机制。

方法

建立大鼠 SCI 模型,并用人参皂苷 Rg1 和核因子红细胞 2 相关因子 2(Nrf2)抑制剂全反式视黄酸(ATRA)进行治疗。通过 Basso、Beattie 和 Bresnahan(BBB)评分、苏木精/伊红染色、ELISA 检测、Western blot 和实时定量 RT-PCR(RT-qPCR)评估人参皂苷 Rg1 的保护作用。

结果

人参皂苷 Rg1 减轻了损伤脊髓中的神经元水肿和出血,减少了炎症细胞浸润和细胞坏死,进一步修复了损伤的脊髓结构,改善了 SCI 大鼠模型的 BBB 运动评分,改善了后肢运动功能。同时,人参皂苷 Rg1 显著增加了抗氧化酶超氧化物歧化酶和谷胱甘肽的含量,并抑制了氧化标志物丙二醛的产生。此外,人参皂苷 Rg1 还显著抑制了肿瘤坏死因子-α、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)等炎症因子的活性,以减轻创伤后的炎症反应。此外,Western blot 和 RT-qPCR 还表明,人参皂苷 Rg1 可在 SCI 后激活 Nrf2 和血红素加氧酶-1(HO-1)的蛋白表达,而 ATRA 对这些改善的抑制作用进一步验证了 Nrf2 和 HO-1 在人参皂苷 Rg1 对 SCI 中的神经保护作用。

结论

人参皂苷 Rg1 对 SCI 具有神经保护作用,并可改善损伤引起的运动功能障碍。其潜在机制可能通过调节 Nrf2/HO-1 信号通路发挥抗氧化应激和抗炎作用。

相似文献

1
Ginsenoside Rg1 inhibits oxidative stress and inflammation in rats with spinal cord injury via Nrf2/HO-1 signaling pathway.人参皂苷 Rg1 通过 Nrf2/HO-1 信号通路抑制脊髓损伤大鼠的氧化应激和炎症。
Neuroreport. 2022 Jan 19;33(2):81-89. doi: 10.1097/WNR.0000000000001757.
2
Ginsenoside Rg1 Protects Cardiomyocytes Against Hypoxia/Reoxygenation Injury via Activation of Nrf2/HO-1 Signaling and Inhibition of JNK.人参皂苷Rg1通过激活Nrf2/HO-1信号通路和抑制JNK保护心肌细胞免受缺氧/复氧损伤。
Cell Physiol Biochem. 2017;44(1):21-37. doi: 10.1159/000484578. Epub 2017 Nov 3.
3
Effects of ginsenoside Rb1 on oxidative stress injury in rat spinal cords by regulating the eNOS/Nrf2/HO-1 signaling pathway.人参皂苷Rb1通过调节eNOS/Nrf2/HO-1信号通路对大鼠脊髓氧化应激损伤的影响
Exp Ther Med. 2018 Aug;16(2):1079-1086. doi: 10.3892/etm.2018.6286. Epub 2018 Jun 12.
4
Polydatin attenuates spinal cord injury in rats by inhibiting oxidative stress and microglia apoptosis via Nrf2/HO-1 pathway.虎杖苷通过 Nrf2/HO-1 通路抑制氧化应激和小胶质细胞凋亡减轻大鼠脊髓损伤。
Life Sci. 2019 Jan 15;217:119-127. doi: 10.1016/j.lfs.2018.11.053. Epub 2018 Nov 24.
5
Zinc promotes functional recovery after spinal cord injury by activating Nrf2/HO-1 defense pathway and inhibiting inflammation of NLRP3 in nerve cells.锌通过激活 Nrf2/HO-1 防御通路和抑制神经细胞中 NLRP3 的炎症反应,促进脊髓损伤后的功能恢复。
Life Sci. 2020 Mar 15;245:117351. doi: 10.1016/j.lfs.2020.117351. Epub 2020 Jan 22.
6
Tetramethylpyrazine improves the recovery of spinal cord injury via Akt/Nrf2/HO-1 pathway.川芎嗪通过Akt/Nrf2/HO-1信号通路促进脊髓损伤的恢复。
Bioorg Med Chem Lett. 2016 Feb 15;26(4):1287-91. doi: 10.1016/j.bmcl.2016.01.015. Epub 2016 Jan 9.
7
α-Cyperone Improves Rat Spinal Cord Tissue Damage via Akt/Nrf2 and NF-κB Pathways.α-环柠檬醛通过 Akt/Nrf2 和 NF-κB 通路改善大鼠脊髓组织损伤。
J Surg Res. 2022 Aug;276:331-339. doi: 10.1016/j.jss.2022.02.006. Epub 2022 Apr 12.
8
Ginsenoside Rg1 regulates astrocytes to promote angiogenesis in spinal cord injury via the JAK2/STAT3 signaling pathway.人参皂苷 Rg1 通过 JAK2/STAT3 信号通路调节星形胶质细胞促进脊髓损伤血管生成。
J Ethnopharmacol. 2024 Nov 15;334:118531. doi: 10.1016/j.jep.2024.118531. Epub 2024 Jul 5.
9
Notoginsenoside R1 alleviates spinal cord injury by inhibiting oxidative stress, neuronal apoptosis, and inflammation via activating the nuclear factor erythroid 2 related factor 2/heme oxygenase-1 signaling pathway.三七皂苷R1通过激活核因子红细胞2相关因子2/血红素加氧酶-1信号通路,抑制氧化应激、神经元凋亡和炎症反应,从而减轻脊髓损伤。
Neuroreport. 2022 Aug 3;33(11):451-462. doi: 10.1097/WNR.0000000000001803. Epub 2022 Jun 27.
10
[NEUROPROTECTIVE EFFECTS OF MANGIFERIN ON ACUTE SPINAL CORD INJURY IN RATS AND ITS MECHANISM].[芒果苷对大鼠急性脊髓损伤的神经保护作用及其机制]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2016 Aug 8;30(8):1019-1025. doi: 10.7507/1002-1892.20160205.

引用本文的文献

1
Mechanistic insights into Nrf2-driven pathogenesis and therapeutic targeting in spinal cord injury.脊髓损伤中Nrf2驱动的发病机制及治疗靶点的机制性见解。
Front Immunol. 2025 Jul 10;16:1574834. doi: 10.3389/fimmu.2025.1574834. eCollection 2025.
2
The role of oxidative stress in spinal cord ischemia reperfusion injury: mechanisms and therapeutic implications.氧化应激在脊髓缺血再灌注损伤中的作用:机制及治疗意义
Front Cell Neurosci. 2025 Jun 24;19:1590493. doi: 10.3389/fncel.2025.1590493. eCollection 2025.
3
Comprehensive understanding and underlying molecular mechanisms of the adaptogenic effects of .
对……适应原性作用的全面理解及其潜在分子机制。 不过你提供的原文不完整,句末应该还有具体所指的事物。
J Ginseng Res. 2025 Jul;49(4):356-365. doi: 10.1016/j.jgr.2025.03.013. Epub 2025 Apr 2.
4
Based on the TLR4/NLRP3 Pathway and Its Impact on the Formation of NETs to Explore the Mechanism of Ginsenoside Rg on Acute Gouty Arthritis.基于TLR4/NLRP3信号通路及其对中性粒细胞胞外陷阱形成的影响探讨人参皂苷Rg对急性痛风性关节炎的作用机制
Int J Mol Sci. 2025 Apr 29;26(9):4233. doi: 10.3390/ijms26094233.
5
Ginsenoside Rg1 in Parkinson's disease: from basic research to clinical applications.人参皂苷Rg1在帕金森病中的应用:从基础研究到临床应用
Front Pharmacol. 2025 Apr 16;16:1490480. doi: 10.3389/fphar.2025.1490480. eCollection 2025.
6
Nrf2 Signaling Pathway: Focus on Oxidative Stress in Spinal Cord Injury.Nrf2信号通路:聚焦脊髓损伤中的氧化应激
Mol Neurobiol. 2025 Feb;62(2):2230-2249. doi: 10.1007/s12035-024-04394-z. Epub 2024 Aug 2.
7
Diabetes cardiomyopathy: targeted regulation of mitochondrial dysfunction and therapeutic potential of plant secondary metabolites.糖尿病心肌病:线粒体功能障碍的靶向调控及植物次生代谢产物的治疗潜力
Front Pharmacol. 2024 Jul 9;15:1401961. doi: 10.3389/fphar.2024.1401961. eCollection 2024.
8
Ginsenoside Rg1 Regulates Immune Microenvironment and Neurological Recovery After Spinal Cord Injury Through MYCBP2 Delivery via Neuronal Cell-Derived Extracellular Vesicles.人参皂苷 Rg1 通过神经元细胞衍生的细胞外囊泡递送 MYCBP2 调节脊髓损伤后的免疫微环境和神经恢复。
Adv Sci (Weinh). 2024 Aug;11(31):e2402114. doi: 10.1002/advs.202402114. Epub 2024 Jun 19.
9
Traditional herbs: mechanisms to combat cellular senescence.传统草药:对抗细胞衰老的机制。
Aging (Albany NY). 2023 Dec 5;15(23):14473-14505. doi: 10.18632/aging.205269.
10
Xiaoxuming decoction cutting formula reduces LPS-stimulated inflammation in BV-2 cells by regulating miR-9-5p in microglia exosomes.消旋去甲乌药碱汤加减方通过调节小胶质细胞外泌体中的miR-9-5p减轻LPS刺激的BV-2细胞炎症。
Front Pharmacol. 2023 May 17;14:1183612. doi: 10.3389/fphar.2023.1183612. eCollection 2023.