• 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
Neuroprotective Mechanisms of PPARδ: Modulation of Oxidative Stress and Inflammatory Processes.过氧化物酶体增殖物激活受体 δ 的神经保护机制:氧化应激和炎症过程的调节。
PPAR Res. 2011;2011:373560. doi: 10.1155/2011/373560. Epub 2011 Oct 29.
2
Novel approach to treat insulin resistance, type 2 diabetes, and the metabolic syndrome: simultaneous activation of PPARalpha, PPARgamma, and PPARdelta.治疗胰岛素抵抗、2型糖尿病和代谢综合征的新方法:同时激活过氧化物酶体增殖物激活受体α、γ和δ
Curr Diabetes Rev. 2005 Aug;1(3):299-307. doi: 10.2174/157339905774574365.
3
Cow's milk increases the activities of human nuclear receptors peroxisome proliferator-activated receptors alpha and delta and retinoid X receptor alpha involved in the regulation of energy homeostasis, obesity, and inflammation.牛奶会增加参与能量平衡、肥胖和炎症调节的人类核受体过氧化物酶体增殖物激活受体α和δ以及视黄酸X受体α的活性。
J Dairy Sci. 2009 Sep;92(9):4180-7. doi: 10.3168/jds.2009-2186.
4
Neuron-specific deletion of peroxisome proliferator-activated receptor delta (PPARδ) in mice leads to increased susceptibility to diet-induced obesity.神经元特异性敲除过氧化物酶体增殖物激活受体 δ (PPARδ) 可导致小鼠对饮食诱导肥胖的易感性增加。
PLoS One. 2012;7(8):e42981. doi: 10.1371/journal.pone.0042981. Epub 2012 Aug 20.
5
Novel peroxisome proliferator-activated receptor (PPAR) gamma and PPARdelta ligands produce distinct biological effects.新型过氧化物酶体增殖物激活受体(PPAR)γ和PPARδ配体产生不同的生物学效应。
J Biol Chem. 1999 Mar 5;274(10):6718-25. doi: 10.1074/jbc.274.10.6718.
6
Functional and Structural Insights into Human PPARα/δ/γ Subtype Selectivity of Bezafibrate, Fenofibric Acid, and Pemafibrate.贝扎贝特、非诺贝特和帕玛贝特对人 PPARα/δ/γ 亚型选择性的功能和结构见解。
Int J Mol Sci. 2022 Apr 25;23(9):4726. doi: 10.3390/ijms23094726.
7
Increased hepatic oxidative metabolism distinguishes the action of Peroxisome proliferator-activated receptor delta from Peroxisome proliferator-activated receptor gamma in the ob/ob mouse.过氧化物酶体增殖物激活受体 δ 与过氧化物酶体增殖物激活受体 γ 在 ob/ob 小鼠中的作用不同,其区别在于前者可增加肝脏的氧化代谢。
Genome Med. 2009 Dec 7;1(12):115. doi: 10.1186/gm115.
8
Peroxisome proliferator-activated receptor agonists and antagonists: a patent review (2014-present).过氧化物酶体增殖物激活受体激动剂和拮抗剂:专利审查(2014 年至今)。
Expert Opin Ther Pat. 2020 Jan;30(1):1-13. doi: 10.1080/13543776.2020.1703952. Epub 2019 Dec 18.
9
Structural basis for specific ligation of the peroxisome proliferator-activated receptor δ.过氧化物酶体增殖物激活受体 δ 的特异性连接的结构基础。
Proc Natl Acad Sci U S A. 2017 Mar 28;114(13):E2563-E2570. doi: 10.1073/pnas.1621513114. Epub 2017 Mar 20.
10
PPAR dual agonists: are they opening Pandora's Box?过氧化物酶体增殖物激活受体双重激动剂:它们是否在打开潘多拉魔盒?
Pharmacol Res. 2007 Aug;56(2):91-8. doi: 10.1016/j.phrs.2007.03.002. Epub 2007 Mar 14.

引用本文的文献

1
Treadmill Exercise Modulates the Leptin/LepR/GSK-3β Signalling Pathway to Improve Leptin Sensitivity and Alleviate Neuroinflammation in High-Fat Diet-Fed APP/PS1 Mice.跑步机运动调节瘦素/瘦素受体/糖原合成酶激酶-3β信号通路,以改善高脂饮食喂养的APP/PS1小鼠的瘦素敏感性并减轻神经炎症。
Mol Neurobiol. 2025 Mar 25. doi: 10.1007/s12035-025-04853-1.
2
Recent Insights on the Role of Nuclear Receptors in Alzheimer's Disease: Mechanisms and Therapeutic Application.核受体在阿尔茨海默病中的作用的最新见解:机制与治疗应用
Int J Mol Sci. 2025 Jan 30;26(3):1207. doi: 10.3390/ijms26031207.
3
Novel PPAR-γ agonists as potential neuroprotective agents against Alzheimer's disease: rational design, synthesis evaluation, PPAR-γ binding assay and transactivation and expression studies.新型PPAR-γ激动剂作为抗阿尔茨海默病的潜在神经保护剂:合理设计、合成评估、PPAR-γ结合测定以及反式激活和表达研究
RSC Adv. 2024 Oct 21;14(45):33247-33266. doi: 10.1039/d4ra06330a. eCollection 2024 Oct 17.
4
Highly potent and selective PPARδ agonist reverses memory deficits in mouse models of Alzheimer's disease.高活性和选择性的过氧化物酶体增殖物激活受体 δ 激动剂可逆转阿尔茨海默病小鼠模型的记忆缺陷。
Theranostics. 2024 Sep 16;14(16):6088-6108. doi: 10.7150/thno.96707. eCollection 2024.
5
High glucose inhibits neural differentiation by excessive autophagy <em>via</em> peroxisome proliferator-activated receptor gamma.高葡萄糖通过过氧化物酶体增殖物激活受体γ诱导过度自噬抑制神经分化。
Eur J Histochem. 2023 May 11;67(2):3691. doi: 10.4081/ejh.2023.3691.
6
The Potential Role of PPARs in the Fetal Origins of Adult Disease.过氧化物酶体增殖物激活受体(PPARs)在成年疾病胎儿起源中的潜在作用。
Cells. 2022 Nov 2;11(21):3474. doi: 10.3390/cells11213474.
7
Cellular and Molecular Regulation of Exercise-A Neuronal Perspective.运动的细胞与分子调节——神经元视角
Cell Mol Neurobiol. 2023 May;43(4):1551-1571. doi: 10.1007/s10571-022-01272-x. Epub 2022 Aug 20.
8
Peroxisomal Proliferator-Activated Receptor / Deficiency Induces Cognitive Alterations.过氧化物酶体增殖物激活受体/缺陷诱导认知改变。
Front Pharmacol. 2022 Jul 11;13:902047. doi: 10.3389/fphar.2022.902047. eCollection 2022.
9
Role of Phytoconstituents as PPAR Agonists: Implications for Neurodegenerative Disorders.植物成分作为过氧化物酶体增殖物激活受体激动剂的作用:对神经退行性疾病的影响。
Biomedicines. 2021 Dec 14;9(12):1914. doi: 10.3390/biomedicines9121914.
10
Tonic Endocannabinoid Signaling Gates Synaptic Plasticity in Dorsal Raphe Nucleus Serotonin Neurons Through Peroxisome Proliferator-Activated Receptors.张力性内源性大麻素信号通过过氧化物酶体增殖物激活受体调节中缝背核5-羟色胺能神经元的突触可塑性
Front Pharmacol. 2021 Jun 28;12:691219. doi: 10.3389/fphar.2021.691219. eCollection 2021.

本文引用的文献

1
GW0742, a high-affinity PPAR-δ agonist, mediates protection in an organotypic model of spinal cord damage.GW0742,一种高亲和力的过氧化物酶体增殖物激活受体-δ激动剂,在脊髓损伤的器官型模型中介导保护作用。
Spine (Phila Pa 1976). 2012 Jan 15;37(2):E73-8. doi: 10.1097/BRS.0b013e3182276d88.
2
Vascular PPARδ protects against stroke-induced brain injury.血管过氧化物酶体增殖物激活受体 δ 对脑卒中诱导的脑损伤具有保护作用。
Arterioscler Thromb Vasc Biol. 2011 Mar;31(3):574-81. doi: 10.1161/ATVBAHA.110.221267. Epub 2011 Jan 4.
3
PPARδ deficient mice develop elevated Th1/Th17 responses and prolonged experimental autoimmune encephalomyelitis.PPARδ 缺陷小鼠会发展出升高的 Th1/Th17 反应和延长的实验性自身免疫性脑脊髓炎。
Brain Res. 2011 Feb 28;1376:101-12. doi: 10.1016/j.brainres.2010.12.059. Epub 2010 Dec 28.
4
Molecular Mechanisms and Genome-Wide Aspects of PPAR Subtype Specific Transactivation.PPAR 亚型特异性转录激活的分子机制和全基因组方面。
PPAR Res. 2010;2010. doi: 10.1155/2010/169506. Epub 2010 Aug 31.
5
PPAR activation has dichotomous control on the expression levels of cytosolic and secretory phospholipase A2 in astrocytes; inhibition in naïve, untreated cells and enhancement in LPS-stimulated cells.过氧化物酶体增殖物激活受体(PPAR)对星形胶质细胞中胞质和分泌型磷脂酶 A2 的表达水平具有双重调控作用;在未处理的原始细胞中抑制,在 LPS 刺激的细胞中增强。
J Neurochem. 2010 Oct;115(2):399-410. doi: 10.1111/j.1471-4159.2010.06931.x. Epub 2010 Aug 25.
6
Peroxisome proliferator-activated receptor delta limits the expansion of pathogenic Th cells during central nervous system autoimmunity.过氧化物酶体增殖物激活受体 δ 限制中枢神经系统自身免疫中致病性 Th 细胞的扩增。
J Exp Med. 2010 Aug 2;207(8):1599-608. doi: 10.1084/jem.20091663. Epub 2010 Jul 12.
7
Impairment of PGC-1alpha expression, neuropathology and hepatic steatosis in a transgenic mouse model of Huntington's disease following chronic energy deprivation.慢性能量剥夺后亨廷顿病转基因小鼠模型中 PGC-1alpha 表达、神经病理学和肝脂肪变性的损伤。
Hum Mol Genet. 2010 Aug 15;19(16):3190-205. doi: 10.1093/hmg/ddq229. Epub 2010 Jun 7.
8
Peroxisome proliferator-activated receptor delta regulation of miR-15a in ischemia-induced cerebral vascular endothelial injury.过氧化物酶体增殖物激活受体 δ 对缺血性脑血管内皮损伤中 miR-15a 的调控作用。
J Neurosci. 2010 May 5;30(18):6398-408. doi: 10.1523/JNEUROSCI.0780-10.2010.
9
Peroxisome-proliferator-activated receptors gamma and peroxisome-proliferator-activated receptors beta/delta and the regulation of interleukin 1 receptor antagonist expression by pioglitazone in ischaemic brain.过氧化物酶体增殖物激活受体 γ 和过氧化物酶体增殖物激活受体 β/δ 以及吡格列酮对缺血性脑内白细胞介素 1 受体拮抗剂表达的调节。
J Hypertens. 2010 Jul;28(7):1488-97. doi: 10.1097/HJH.0b013e3283396e4e.
10
Peroxisome proliferator-activated receptor delta agonists inhibit T helper type 1 (Th1) and Th17 responses in experimental allergic encephalomyelitis.过氧化物酶体增殖物激活受体 δ 激动剂可抑制实验性变态反应性脑脊髓炎中的辅助性 T 细胞 1(Th1)和 Th17 反应。
Immunology. 2010 Aug;130(4):572-88. doi: 10.1111/j.1365-2567.2010.03261.x. Epub 2010 Apr 6.

过氧化物酶体增殖物激活受体 δ 的神经保护机制:氧化应激和炎症过程的调节。

Neuroprotective Mechanisms of PPARδ: Modulation of Oxidative Stress and Inflammatory Processes.

机构信息

Department of Cancer Biology, Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

PPAR Res. 2011;2011:373560. doi: 10.1155/2011/373560. Epub 2011 Oct 29.

DOI:10.1155/2011/373560
PMID:22135673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3205692/
Abstract

Peroxisome proliferator-activated receptors (PPARα, δ, and γ) are ligand-activated transcription factors that regulate a wide range of cellular processes, including inflammation, proliferation, differentiation, metabolism, and energy homeostasis. All three PPAR subtypes have been identified in the central nervous system (CNS) of rodents. While PPARα and PPARγ are expressed in more restricted areas of the CNS, PPARδ is ubiquitously expressed and is the predominant subtype. Although data regarding PPARδ are limited, studies have demonstrated that administration of PPARδ agonists confers neuroprotection following various acute and chronic injuries to the CNS, such as stroke, multiple sclerosis, and Alzheimer's disease. The antioxidant and anti-inflammatory properties of PPARδ agonists are thought to underly their neuroprotective efficacy. This review will focus on the putative neuroprotective benefits of therapeutically targeting PPARδ in the CNS, and specifically, highlight the antioxidant and anti-inflammatory functions of PPARδ agonists.

摘要

过氧化物酶体增殖物激活受体 (PPARα、δ 和 γ) 是配体激活的转录因子,可调节多种细胞过程,包括炎症、增殖、分化、代谢和能量稳态。这三种 PPAR 亚型在啮齿动物的中枢神经系统 (CNS) 中均有发现。虽然 PPARα 和 PPARγ 在 CNS 的限定区域表达,但 PPARδ 广泛表达,是主要的亚型。尽管关于 PPARδ 的数据有限,但研究表明,在中枢神经系统受到各种急性和慢性损伤(如中风、多发性硬化症和阿尔茨海默病)后,给予 PPARδ 激动剂可提供神经保护作用。PPARδ 激动剂的抗氧化和抗炎特性被认为是其神经保护作用的基础。这篇综述将重点介绍在中枢神经系统中靶向治疗 PPARδ 的潜在神经保护益处,并特别强调 PPARδ 激动剂的抗氧化和抗炎功能。