• 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

过氧化物酶体增殖物激活受体激动剂对神经胶质细胞激活的调节:与中枢神经系统炎症性疾病的相关性

Peroxisome proliferator-activated receptor agonist regulation of glial activation: relevance to CNS inflammatory disorders.

作者信息

Drew Paul D, Xu Jihong, Storer Paul D, Chavis Janet A, Racke Michael K

机构信息

Department of Neurobiology and Developmental Sciences, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. drewpauld @uams.edu

出版信息

Neurochem Int. 2006 Jul;49(2):183-9. doi: 10.1016/j.neuint.2006.04.003. Epub 2006 Jun 5.

DOI:10.1016/j.neuint.2006.04.003
PMID:16753239
Abstract

Peroxisome proliferator-activated receptors (PPARs) play key roles in lipid metabolism and inflammation. Recent studies indicated that PPARs are also capable of modulating immune responses. Microglia and astrocytes are cells resident to the central nervous system (CNS) that function to protect against environmental insults including pathogens. However, following CNS inflammation, reactive gliosis occurs which is characterized by astrocyte hypertrophy and increased glial proliferation. Under such conditions, glia can become chronically activated and may contribute to the neuropathology associated with a variety of neuroinflammatory disorders including multiple sclerosis (MS), Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS), and stroke. A review of the role of PPAR agonists in modulating glial cell activation is presented. Included is a discussion of the molecular mechanisms of action of these PPAR agonists and the potential utility of these agents for the treatment of neuroinflammatory disorders.

摘要

过氧化物酶体增殖物激活受体(PPARs)在脂质代谢和炎症中发挥关键作用。最近的研究表明,PPARs也能够调节免疫反应。小胶质细胞和星形胶质细胞是中枢神经系统(CNS)中的常驻细胞,其功能是抵御包括病原体在内的环境侵害。然而,在中枢神经系统发生炎症后,会出现反应性胶质增生,其特征是星形胶质细胞肥大和胶质细胞增殖增加。在这种情况下,胶质细胞可能会长期激活,并可能导致与多种神经炎症性疾病相关的神经病理学变化,包括多发性硬化症(MS)、阿尔茨海默病(AD)、帕金森病(PD)、肌萎缩侧索硬化症(ALS)和中风。本文综述了PPAR激动剂在调节胶质细胞激活中的作用。其中包括对这些PPAR激动剂作用的分子机制以及这些药物在治疗神经炎症性疾病方面潜在效用的讨论。

相似文献

1
Peroxisome proliferator-activated receptor agonist regulation of glial activation: relevance to CNS inflammatory disorders.过氧化物酶体增殖物激活受体激动剂对神经胶质细胞激活的调节:与中枢神经系统炎症性疾病的相关性
Neurochem Int. 2006 Jul;49(2):183-9. doi: 10.1016/j.neuint.2006.04.003. Epub 2006 Jun 5.
2
Discovery of a new class of synthetic protein kinase inhibitors that suppress selective aspects of glial activation and protect against beta-amyloid induced injury: a foundation for future medicinal chemistry efforts focused on targeting Alzheimer's disease progression.发现一类新型合成蛋白激酶抑制剂,其可抑制神经胶质细胞激活的某些特定方面并预防β-淀粉样蛋白诱导的损伤:这为未来专注于靶向阿尔茨海默病进展的药物化学研究奠定了基础。
J Mol Neurosci. 2003;20(3):411-23. doi: 10.1385/JMN:20:3:411.
3
Catalpol attenuates the neurotoxicity induced by beta-amyloid(1-42) in cortical neuron-glia cultures.梓醇减轻β-淀粉样蛋白(1-42)在皮层神经元-神经胶质细胞培养物中诱导的神经毒性。
Brain Res. 2008 Jan 10;1188:139-47. doi: 10.1016/j.brainres.2007.07.105. Epub 2007 Oct 22.
4
Multifunctional effects of bradykinin on glial cells in relation to potential anti-inflammatory effects.缓激肽对神经胶质细胞的多功能作用及其潜在的抗炎作用
Neurochem Int. 2007 Jul-Sep;51(2-4):185-91. doi: 10.1016/j.neuint.2007.06.017. Epub 2007 Jun 27.
5
IL-4-induced peroxisome proliferator-activated receptor gamma activation inhibits NF-kappaB trans activation in central nervous system (CNS) glial cells and protects oligodendrocyte progenitors under neuroinflammatory disease conditions: implication for CNS-demyelinating diseases.白细胞介素-4诱导的过氧化物酶体增殖物激活受体γ激活抑制中枢神经系统(CNS)神经胶质细胞中的核因子-κB反式激活,并在神经炎性疾病条件下保护少突胶质前体细胞:对中枢神经系统脱髓鞘疾病的意义。
J Immunol. 2006 Apr 1;176(7):4385-98. doi: 10.4049/jimmunol.176.7.4385.
6
PPAR agonists for the treatment of neuroinflammatory diseases.过氧化物酶体增殖物激活受体激动剂治疗神经炎症性疾病。
Trends Pharmacol Sci. 2024 Jan;45(1):9-23. doi: 10.1016/j.tips.2023.11.004. Epub 2023 Dec 7.
7
Peroxisome proliferator-activated receptors (PPARs) agonists as promising neurotherapeutics.过氧化物酶体增殖物激活受体(PPARs)激动剂有望成为神经治疗药物。
Bioorg Chem. 2025 Mar;156:108226. doi: 10.1016/j.bioorg.2025.108226. Epub 2025 Jan 30.
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
Metabolic and Inflammatory Adaptation of Reactive Astrocytes: Role of PPARs.反应性星形胶质细胞的代谢和炎症适应性:过氧化物酶体增殖物激活受体的作用
Mol Neurobiol. 2017 May;54(4):2518-2538. doi: 10.1007/s12035-016-9833-2. Epub 2016 Mar 17.
10
Prostaglandins and cyclooxygenases in glial cells during brain inflammation.脑炎症期间神经胶质细胞中的前列腺素和环氧化酶
Curr Drug Targets Inflamm Allergy. 2005 Jun;4(3):335-40. doi: 10.2174/1568010054022051.

引用本文的文献

1
EBV-Derived miR-BART20-3p Influences Proliferation and Migration in EBV-Positive Gastric Cancer Models by Suppressing PPARα.EB病毒衍生的miR-BART20-3p通过抑制PPARα影响EB病毒阳性胃癌模型中的细胞增殖和迁移。
Microorganisms. 2025 Jun 28;13(7):1514. doi: 10.3390/microorganisms13071514.
2
Therapeutic modulation of JAK-STAT, mTOR, and PPAR-γ signaling in neurological dysfunctions.神经功能障碍中 JAK-STAT、mTOR 和 PPAR-γ 信号的治疗调节。
J Mol Med (Berl). 2023 Feb;101(1-2):9-49. doi: 10.1007/s00109-022-02272-6. Epub 2022 Dec 7.
3
Risk Factors for Retinal Ganglion Cell Distress in Glaucoma and Neuroprotective Potential Intervention.
青光眼视网膜神经节细胞损伤的风险因素和神经保护的潜在干预作用。
Int J Mol Sci. 2021 Jul 27;22(15):7994. doi: 10.3390/ijms22157994.
4
Comparison of PPAR Ligands as Modulators of Resolution of Inflammation, via Their Influence on Cytokines and Oxylipins Release in Astrocytes.比较过氧化物酶体增殖物激活受体配体作为炎症消退的调节剂,通过它们对星形胶质细胞细胞因子和氧化脂类释放的影响。
Int J Mol Sci. 2020 Dec 16;21(24):9577. doi: 10.3390/ijms21249577.
5
Understanding the Multiple Effects of PCBs on Lipid Metabolism.了解多氯联苯对脂质代谢的多种影响。
Diabetes Metab Syndr Obes. 2020 Oct 13;13:3691-3702. doi: 10.2147/DMSO.S264851. eCollection 2020.
6
Methamphetamine and Cannabis: A Tale of Two Drugs and their Effects on HIV, Brain, and Behavior.甲基苯丙胺和大麻:两种药物及其对 HIV、大脑和行为影响的故事。
J Neuroimmune Pharmacol. 2020 Dec;15(4):743-764. doi: 10.1007/s11481-020-09957-0. Epub 2020 Sep 15.
7
Intracerebral hemorrhage alters circular RNA expression profiles in the rat brain.脑出血改变大鼠脑内环状RNA表达谱。
Am J Transl Res. 2020 Aug 15;12(8):4160-4174. eCollection 2020.
8
Radiation-induced brain injury: current concepts and therapeutic strategies targeting neuroinflammation.辐射诱导的脑损伤:针对神经炎症的当前概念和治疗策略
Neurooncol Adv. 2020 May 5;2(1):vdaa057. doi: 10.1093/noajnl/vdaa057. eCollection 2020 Jan-Dec.
9
Prostaglandins as the Agents That Modulate the Course of Brain Disorders.前列腺素作为调节脑部疾病进程的因子。
Degener Neurol Neuromuscul Dis. 2020 Jan 16;10:1-13. doi: 10.2147/DNND.S240800. eCollection 2020.
10
Mitochondrial biogenesis is altered in HIV+ brains exposed to ART: Implications for therapeutic targeting of astroglia.HIV 感染者大脑中接受 ART 治疗后会发生线粒体生物发生改变:针对星形胶质细胞的治疗靶向的意义。
Neurobiol Dis. 2019 Oct;130:104502. doi: 10.1016/j.nbd.2019.104502. Epub 2019 Jun 22.