• 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

相似文献

1
Go-sha-jinki-Gan Alleviates Inflammation in Neurological Disorders via p38-TNF Signaling in the Central Nervous System.过岗龙津甘通过中枢神经系统 p38-TNF 信号减轻神经紊乱中的炎症。
Neurotherapeutics. 2021 Jan;18(1):460-473. doi: 10.1007/s13311-020-00948-w. Epub 2020 Oct 20.
2
Go-sha-jinki-Gan (GJG) ameliorates allodynia in chronic constriction injury-model mice via suppression of TNF-α expression in the spinal cord.桂枝加荆芥防风汤(GJG)通过抑制脊髓中肿瘤坏死因子-α(TNF-α)的表达来改善慢性缩窄损伤模型小鼠的痛觉过敏。
Mol Pain. 2016 Jun 13;12. doi: 10.1177/1744806916656382. Print 2016.
3
Gosha-jinki-Gan (GJG) shows anti-aging effects through suppression of TNF-α production by Chikusetsusaponin V.柴胡皂甙 V 通过抑制 TNF-α 的产生发挥抗衰老作用。
Gene. 2022 Mar 20;815:146178. doi: 10.1016/j.gene.2021.146178. Epub 2022 Jan 4.
4
Go-sha-jinki-Gan (GJG), a traditional Japanese herbal medicine, protects against sarcopenia in senescence-accelerated mice.五倍子人参汤(GJG)是一种传统的日本草药,可预防衰老加速小鼠的肌肉减少症。
Phytomedicine. 2015 Jan 15;22(1):16-22. doi: 10.1016/j.phymed.2014.11.005. Epub 2014 Nov 20.
5
Alpha-lipoic acid improved motor function in MPTP-induced Parkinsonian mice by reducing neuroinflammation in the nigral and spinal cord.硫辛酸通过减少黑质和脊髓中的神经炎症改善了 MPTP 诱导的帕金森病小鼠的运动功能。
Neurosci Lett. 2022 Jun 11;781:136669. doi: 10.1016/j.neulet.2022.136669. Epub 2022 Apr 29.
6
Levocorydalmine attenuates microglia activation and neuropathic pain by suppressing ASK1-p38 MAPK/NF-κB signaling pathways in rat spinal cord.左西孟旦通过抑制大鼠脊髓中的 ASK1-p38 MAPK/NF-κB 信号通路来减轻小胶质细胞激活和神经病理性疼痛。
Reg Anesth Pain Med. 2020 Mar;45(3):219-229. doi: 10.1136/rapm-2019-100875. Epub 2020 Jan 2.
7
MPTP activates ASK1-p38 MAPK signaling pathway through TNF-dependent Trx1 oxidation in parkinsonism mouse model.在帕金森病小鼠模型中,MPTP通过肿瘤坏死因子(TNF)依赖的硫氧还蛋白1(Trx1)氧化激活ASK1-p38丝裂原活化蛋白激酶(MAPK)信号通路。
Free Radic Biol Med. 2015 Oct;87:312-25. doi: 10.1016/j.freeradbiomed.2015.06.041. Epub 2015 Jul 9.
8
RAM-589.555 favors neuroprotective and anti-inflammatory profile of CNS-resident glial cells in acute relapse EAE affected mice.RAM-589.555 有利于急性复发 EAE 影响的小鼠中枢神经系统驻留神经胶质细胞的神经保护和抗炎特性。
J Neuroinflammation. 2020 Oct 21;17(1):313. doi: 10.1186/s12974-020-01983-2.
9
Targeting the RNA-Binding Protein HuR Alleviates Neuroinflammation in Experimental Autoimmune Encephalomyelitis: Potential Therapy for Multiple Sclerosis.靶向 RNA 结合蛋白 HuR 可减轻实验性自身免疫性脑脊髓炎的神经炎症:多发性硬化症的潜在治疗方法。
Neurotherapeutics. 2021 Jan;18(1):412-429. doi: 10.1007/s13311-020-00958-8. Epub 2020 Nov 16.
10
Ginsenoside Rg1 attenuates motor impairment and neuroinflammation in the MPTP-probenecid-induced parkinsonism mouse model by targeting α-synuclein abnormalities in the substantia nigra.人参皂苷 Rg1 通过靶向黑质中异常的α-突触核蛋白减轻 MPTP-丙磺舒诱导的帕金森病模型中的运动障碍和神经炎症。
Toxicol Lett. 2016 Jan 22;243:7-21. doi: 10.1016/j.toxlet.2015.12.005. Epub 2015 Dec 23.

引用本文的文献

1
Temporal changes of spinal microglia in murine models of neuropathic pain: a scoping review.神经性疼痛小鼠模型中脊髓小胶质细胞的时间变化:一项范围综述
Front Immunol. 2024 Dec 6;15:1460072. doi: 10.3389/fimmu.2024.1460072. eCollection 2024.
2
Role of microglia in diabetic neuropathic pain.小胶质细胞在糖尿病性神经病理性疼痛中的作用。
Front Cell Dev Biol. 2024 Jul 29;12:1421191. doi: 10.3389/fcell.2024.1421191. eCollection 2024.
3
Pathological mechanisms and treatment of sporadic Parkinson's disease: past, present, and future.散发性帕金森病的病理机制和治疗:过去、现在和未来。
J Neural Transm (Vienna). 2024 Jun;131(6):597-607. doi: 10.1007/s00702-024-02788-w. Epub 2024 Jun 12.
4
Behavioral and Immunohistochemical Evidence for Suppressive Effects of Goshajinkigan on Salicylate-Induced Tinnitus in Rats.八味地黄丸对大鼠水杨酸盐诱导耳鸣抑制作用的行为学及免疫组化证据
Brain Sci. 2022 Apr 30;12(5):587. doi: 10.3390/brainsci12050587.

本文引用的文献

1
Microglia Biology: One Century of Evolving Concepts.小胶质细胞生物学:百年演变概念。
Cell. 2019 Oct 3;179(2):292-311. doi: 10.1016/j.cell.2019.08.053.
2
Neuroprotective and Antioxidant Effect of Ginkgo biloba Extract Against AD and Other Neurological Disorders.银杏叶提取物对 AD 及其他神经退行性疾病的神经保护和抗氧化作用。
Neurotherapeutics. 2019 Jul;16(3):666-674. doi: 10.1007/s13311-019-00767-8.
3
MicroRNA-124 regulates the expression of p62/p38 and promotes autophagy in the inflammatory pathogenesis of Parkinson's disease.MicroRNA-124 调节 p62/p38 的表达,促进帕金森病炎症发病机制中的自噬。
FASEB J. 2019 Jul;33(7):8648-8665. doi: 10.1096/fj.201900363R. Epub 2019 Apr 17.
4
Brain regulatory T cells suppress astrogliosis and potentiate neurological recovery.脑调节性 T 细胞抑制星形胶质细胞增生并增强神经功能恢复。
Nature. 2019 Jan;565(7738):246-250. doi: 10.1038/s41586-018-0824-5. Epub 2019 Jan 2.
5
P38 Mitogen-activated Protein Kinase and Parkinson's Disease.P38丝裂原活化蛋白激酶与帕金森病
Transl Neurosci. 2018 Nov 12;9:147-153. doi: 10.1515/tnsci-2018-0022. eCollection 2018.
6
Microglia in neurodegeneration.神经退行性疾病中的小胶质细胞。
Nat Neurosci. 2018 Oct;21(10):1359-1369. doi: 10.1038/s41593-018-0242-x. Epub 2018 Sep 26.
7
Promises and limitations of immune cell-based therapies in neurological disorders.免疫细胞疗法在神经退行性疾病中的应用前景及局限性。
Nat Rev Neurol. 2018 Sep;14(9):559-568. doi: 10.1038/s41582-018-0028-5.
8
An Inflammation-Centric View of Neurological Disease: Beyond the Neuron.以炎症为中心的神经疾病观:超越神经元
Front Cell Neurosci. 2018 Mar 21;12:72. doi: 10.3389/fncel.2018.00072. eCollection 2018.
9
The roles of macrophages and microglia in multiple sclerosis and experimental autoimmune encephalomyelitis.巨噬细胞和小胶质细胞在多发性硬化症和实验性自身免疫性脑脊髓炎中的作用。
J Neuroimmunol. 2018 May 15;318:1-7. doi: 10.1016/j.jneuroim.2018.02.015. Epub 2018 Feb 27.
10
Novel disease-modifying anti-rheumatic drug iguratimod suppresses chronic experimental autoimmune encephalomyelitis by down-regulating activation of macrophages/microglia through an NF-κB pathway.新型疾病修饰抗风湿药物依古珠单抗通过 NF-κB 通路下调巨噬细胞/小胶质细胞的激活来抑制慢性实验性自身免疫性脑脊髓炎。
Sci Rep. 2018 Jan 31;8(1):1933. doi: 10.1038/s41598-018-20390-5.

过岗龙津甘通过中枢神经系统 p38-TNF 信号减轻神经紊乱中的炎症。

Go-sha-jinki-Gan Alleviates Inflammation in Neurological Disorders via p38-TNF Signaling in the Central Nervous System.

机构信息

Department of Neurology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.

Department of Health Development and Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.

出版信息

Neurotherapeutics. 2021 Jan;18(1):460-473. doi: 10.1007/s13311-020-00948-w. Epub 2020 Oct 20.

DOI:10.1007/s13311-020-00948-w
PMID:33083995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8116410/
Abstract

Go-sha-jinki-Gan (GJG) is a traditional Japanese herbal medicine. In clinical practice, GJG is effective against neuropathic pain and hypersensitivity induced by chemotherapy or diabetes. In our previous study using a chronic constriction injury mouse model, we showed that GJG inhibited microglia activation by suppressing the expression of tumor necrosis factor-α (TNF-α) and p38 mitogen-activated protein kinase (p38 MAPK) in the peripheral nervous system. To investigate whether GJG can suppress inflammation in the central nervous system (CNS) in the context of neurological disorders, we examined the effect of GJG on the activation of resident glial cells and on p38-TNF signaling in two mouse models of neurological disorders: the experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis and the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model of Parkinson's disease. GJG administration relieved the severity of clinical EAE symptoms and MPTP-induced inflammation by decreasing the number of microglia and the production of TNF-α in the spinal cord of EAE mice and the substantia nigra of MPTP-treated mice. Accordingly, GJG suppressed the phosphorylation of p38 in glial cells of these two mouse models. We conclude that GJG attenuates inflammation of the CNS by suppressing glial cell activation, followed by a decrease in the production of TNF-α via p38-TNF signaling.

摘要

葛根芩连汤是一种传统的日本草药。在临床实践中,葛根芩连汤对化疗或糖尿病引起的神经病理性疼痛和超敏反应有效。在我们之前使用慢性缩窄损伤小鼠模型的研究中,我们表明葛根芩连汤通过抑制肿瘤坏死因子-α(TNF-α)和丝裂原活化蛋白激酶 p38(p38 MAPK)在外周神经系统中的表达来抑制小胶质细胞激活。为了研究葛根芩连汤是否可以抑制神经紊乱时中枢神经系统(CNS)的炎症,我们研究了葛根芩连汤对两种神经紊乱小鼠模型中神经胶质细胞激活和 p38-TNF 信号的影响:多发性硬化的实验性自身免疫性脑脊髓炎(EAE)模型和帕金森病的 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)模型。葛根芩连汤通过减少 EAE 小鼠脊髓和 MPTP 处理小鼠黑质中小胶质细胞数量和 TNF-α的产生,缓解了 EAE 症状的严重程度和 MPTP 诱导的炎症。相应地,葛根芩连汤抑制了这两种小鼠模型中神经胶质细胞中 p38 的磷酸化。我们得出结论,葛根芩连汤通过抑制神经胶质细胞激活来减轻 CNS 炎症,随后通过 p38-TNF 信号减少 TNF-α的产生。