• 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

硫化氢通过抑制 p38MAPK/mTOR/NF-κB 信号通路清除自由基改善脊髓损伤。

Hydrogen Sulfide can Scavenge Free Radicals to Improve Spinal Cord Injury by Inhibiting the p38MAPK/mTOR/NF-κB Signaling Pathway.

机构信息

Department of Histology and Embryology, School of Medicine, Shaoxing University, Shaoxing, 312000, Zhejiang Province, China.

出版信息

Neuromolecular Med. 2024 Jun 21;26(1):26. doi: 10.1007/s12017-024-08794-1.

DOI:10.1007/s12017-024-08794-1
PMID:38907170
Abstract

Spinal cord injury (SCI) causes irreversible cell loss and neurological dysfunctions. Presently, there is no an effective clinical treatment for SCI. It can be the only intervention measure by relieving the symptoms of patients such as pain and fever. Free radical-induced damage is one of the validated mechanisms in the complex secondary injury following primary SCI. Hydrogen sulfide (HS) as an antioxidant can effectively scavenge free radicals, protect neurons, and improve SCI by inhibiting the p38MAPK/mTOR/NF-κB signaling pathway. In this report, we analyze the pathological mechanism of SCI, the role of free radical-mediated the p38MAPK/mTOR/NF-κB signaling pathway in SCI, and the role of HS in scavenging free radicals and improving SCI.

摘要

脊髓损伤 (SCI) 会导致不可逆转的细胞死亡和神经功能障碍。目前,SCI 没有有效的临床治疗方法。它只能通过缓解患者的疼痛和发烧等症状来作为唯一的干预措施。自由基诱导的损伤是原发性 SCI 后复杂继发性损伤的已验证机制之一。硫化氢 (HS) 作为一种抗氧化剂,可通过抑制 p38MAPK/mTOR/NF-κB 信号通路有效清除自由基、保护神经元,并改善 SCI。在本报告中,我们分析了 SCI 的病理机制、自由基介导的 p38MAPK/mTOR/NF-κB 信号通路在 SCI 中的作用以及 HS 清除自由基和改善 SCI 的作用。

相似文献

1
Hydrogen Sulfide can Scavenge Free Radicals to Improve Spinal Cord Injury by Inhibiting the p38MAPK/mTOR/NF-κB Signaling Pathway.硫化氢通过抑制 p38MAPK/mTOR/NF-κB 信号通路清除自由基改善脊髓损伤。
Neuromolecular Med. 2024 Jun 21;26(1):26. doi: 10.1007/s12017-024-08794-1.
2
Down-regulation of PGAM5 attenuates spinal cord injury-induced neuronal injury by inhibiting ASK-1/p38/NF-kB signaling.PGAM5的下调通过抑制ASK-1/p38/NF-κB信号传导减轻脊髓损伤诱导的神经元损伤。
Folia Neuropathol. 2024 Aug 21. doi: 10.5114/fn.2024.141372.
3
The beneficial effect of α-lipoic acid on spinal cord injury repair in rats is mediated through inhibition of oxidative stress: A transcriptomic analysis.α-硫辛酸对大鼠脊髓损伤修复的有益作用是通过抑制氧化应激介导的:一项转录组学分析。
J Spinal Cord Med. 2024 Apr 22:1-14. doi: 10.1080/10790268.2024.2342058.
4
Influence and molecular mechanism of cinnamaldehyde against ventricular arrhythmia via the TAK1-p38MAPK-NLRP3 pathway.肉桂醛通过TAK1-p38MAPK-NLRP3通路抗室性心律失常的作用及分子机制
Heart Vessels. 2025 Mar 27. doi: 10.1007/s00380-025-02529-3.
5
The Circadian Clock Gene Bmal1 Regulates Microglial Pyroptosis After Spinal Cord Injury via NF-κB/MMP9.昼夜节律钟基因Bmal1通过NF-κB/MMP9调节脊髓损伤后小胶质细胞焦亡。
CNS Neurosci Ther. 2024 Dec;30(12):e70130. doi: 10.1111/cns.70130.
6
BHLHE40 regulates microglia polarization after spinal cord injury via the NF-κB pathway.BHLHE40通过NF-κB信号通路调控脊髓损伤后小胶质细胞的极化。
Brain Res Bull. 2025 Jan;220:111139. doi: 10.1016/j.brainresbull.2024.111139. Epub 2024 Nov 23.
7
MAPK signaling pathway in spinal cord injury: Mechanisms and therapeutic potential.脊髓损伤中的 MAPK 信号通路:机制与治疗潜力。
Exp Neurol. 2025 Jan;383:115043. doi: 10.1016/j.expneurol.2024.115043. Epub 2024 Nov 8.
8
Exploring the molecular mechanism of icariin improving spinal cord injury through network pharmacology combined with experimental verification.通过网络药理学结合实验验证探索淫羊藿苷改善脊髓损伤的分子机制。
Naunyn Schmiedebergs Arch Pharmacol. 2025 Feb 27. doi: 10.1007/s00210-025-03904-7.
9
Activation of the Nrf2 Signaling Pathway by Tetrahydroberberine Suppresses Ferroptosis and Enhances Functional Recovery Following Spinal Cord Injury.四氢小檗碱激活Nrf2信号通路可抑制脊髓损伤后的铁死亡并促进功能恢复。
Mol Neurobiol. 2025 Feb 26. doi: 10.1007/s12035-025-04791-y.
10
Ferroptosis inhibitor improves outcome after early and delayed treatment in mild spinal cord injury.铁死亡抑制剂可改善轻度脊髓损伤的早期和延迟治疗后的结局。
Acta Neuropathol. 2024 Jun 22;147(1):106. doi: 10.1007/s00401-024-02758-2.

引用本文的文献

1
Mitochondria: the hidden engines of traumatic brain injury-driven neurodegeneration.线粒体:创伤性脑损伤所致神经退行性变的隐匿引擎
Front Cell Neurosci. 2025 May 9;19:1570596. doi: 10.3389/fncel.2025.1570596. eCollection 2025.
2
Hydrogen Sulfide Modulates Microglial Polarization and Remodels the Injury Microenvironment to Promote Functional Recovery After Spinal Cord Injury.硫化氢调节小胶质细胞极化并重塑损伤微环境以促进脊髓损伤后的功能恢复。
CNS Neurosci Ther. 2025 May;31(5):e70431. doi: 10.1111/cns.70431.
3
Effect of hydrogen sulfide on alpha-synuclein aggregation and cell viability.

本文引用的文献

1
Enhanced hepatotoxicity in zebrafish due to co-exposure of microplastics and sulfamethoxazole: Insights into ROS-mediated MAPK signaling pathway regulation.由于微塑料和磺胺甲恶唑的共同暴露,斑马鱼的肝毒性增强:对 ROS 介导的 MAPK 信号通路调控的深入了解。
Ecotoxicol Environ Saf. 2024 Jun 15;278:116415. doi: 10.1016/j.ecoenv.2024.116415. Epub 2024 May 3.
2
Caffeic acid phenethyl ester inhibits neuro-inflammation and oxidative stress following spinal cord injury by mitigating mitochondrial dysfunction via the SIRT1/PGC1α/DRP1 signaling pathway.绿原酸苯乙酯通过 SIRT1/PGC1α/DRP1 信号通路减轻线粒体功能障碍抑制脊髓损伤后的神经炎症和氧化应激。
J Transl Med. 2024 Mar 25;22(1):304. doi: 10.1186/s12967-024-05089-8.
3
硫化氢对α-突触核蛋白聚集及细胞活力的影响。
Sci Rep. 2025 May 4;15(1):15597. doi: 10.1038/s41598-025-99794-z.
4
Amantadine modulates novel macrophage phenotypes to enhance neural repair following spinal cord injury.金刚烷胺可调节新型巨噬细胞表型,以促进脊髓损伤后的神经修复。
J Transl Med. 2025 Jan 13;23(1):60. doi: 10.1186/s12967-024-05916-y.
Role of the NF-kB signalling pathway in heterotopic ossification: biological and therapeutic significance.
NF-κB 信号通路在异位骨化中的作用:生物学和治疗意义。
Cell Commun Signal. 2024 Mar 4;22(1):159. doi: 10.1186/s12964-024-01533-w.
4
Sarsasapogenin regulates the immune microenvironment through MAPK/NF-kB signaling pathway and promotes functional recovery after spinal cord injury.菝葜皂苷元通过MAPK/NF-κB信号通路调节免疫微环境并促进脊髓损伤后的功能恢复。
Heliyon. 2024 Jan 26;10(3):e25145. doi: 10.1016/j.heliyon.2024.e25145. eCollection 2024 Feb 15.
5
Metabolomic Signatures of Brainstem in Mice following Acute and Subchronic Hydrogen Sulfide Exposure.急性和亚慢性硫化氢暴露后小鼠脑干的代谢组学特征
Metabolites. 2024 Jan 14;14(1):53. doi: 10.3390/metabo14010053.
6
A slow-releasing donor of hydrogen sulfide inhibits neuronal cell death via anti-PANoptosis in rats with spinal cord ischemia‒reperfusion injury.一种缓慢释放的硫化氢供体通过抗 PANoptosis 抑制脊髓缺血再灌注损伤大鼠神经元细胞死亡。
Cell Commun Signal. 2024 Jan 12;22(1):33. doi: 10.1186/s12964-023-01457-x.
7
A role for the cystathionine-β-synthase /HS axis in astrocyte dysfunction in the aging brain.胱硫醚-β-合酶/硫化氢轴在衰老大脑星形胶质细胞功能障碍中的作用。
Redox Biol. 2023 Dec;68:102958. doi: 10.1016/j.redox.2023.102958. Epub 2023 Nov 6.
8
Anti-Neuroinflammatory Effect of the Ethanolic Extract of Black Ginseng through TLR4-MyD88-Regulated Inhibition of NF-κB and MAPK Signaling Pathways in LPS-Induced BV2 Microglial Cells.黑参的醇提物通过 TLR4-MyD88 调控的 NF-κB 和 MAPK 信号通路抑制 LPS 诱导的 BV2 小胶质细胞的神经炎症作用。
Int J Mol Sci. 2023 Oct 18;24(20):15320. doi: 10.3390/ijms242015320.
9
Unbiased multitissue transcriptomic analysis reveals complex neuroendocrine regulatory networks mediated by spinal cord injury-induced immunodeficiency.无偏多组织转录组分析揭示了由脊髓损伤诱导的免疫缺陷介导的复杂神经内分泌调节网络。
J Neuroinflammation. 2023 Sep 30;20(1):219. doi: 10.1186/s12974-023-02906-7.
10
Chlorogenic Acid Alleviates LPS-Induced Inflammation and Oxidative Stress by Modulating CD36/AMPK/PGC-1α in RAW264.7 Macrophages.绿原酸通过调控 RAW264.7 巨噬细胞中的 CD36/AMPK/PGC-1α 减轻 LPS 诱导的炎症和氧化应激。
Int J Mol Sci. 2023 Aug 31;24(17):13516. doi: 10.3390/ijms241713516.