• 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

金丝桃苷通过体外糖基化终产物刺激,通过 c-Jun N-末端激酶(JNK)通路下调晚期糖基化终产物受体(RAGE),并促进 ECV304 细胞增殖。

Hyperoside downregulates the receptor for advanced glycation end products (RAGE) and promotes proliferation in ECV304 cells via the c-Jun N-terminal kinases (JNK) pathway following stimulation by advanced glycation end-products in vitro.

机构信息

Sericulture & Agri-Food Research Institute, Guangdong Academy of Agricultural Sciences, NO. 133 Yiheng St. Dongguanzhuang Rd., Tianhe Ditrict, Guangzhou 510610, China.

出版信息

Int J Mol Sci. 2013 Nov 18;14(11):22697-707. doi: 10.3390/ijms141122697.

DOI:10.3390/ijms141122697
PMID:24252909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3856085/
Abstract

Hyperoside is a major active constituent in many medicinal plants which are traditionally used in Chinese medicines for their neuroprotective, anti-inflammatory and antioxidative effects. The molecular mechanisms underlying these effects are unknown. In this study, quiescent ECV304 cells were treated in vitro with advanced glycation end products (AGEs) in the presence or absence of hyperoside. The results demonstrated that AGEs induced c-Jun N-terminal kinases (JNK) activation and apoptosis in ECV304 cells. Hyperoside inhibited these effects and promoted ECV304 cell proliferation. Furthermore, hyperoside significantly inhibited RAGE expression in AGE-stimulated ECV304 cells, whereas knockdown of RAGE inhibited AGE-induced JNK activation. These results suggested that AGEs may promote JNK activation, leading to viability inhibition of ECV304 cells via the RAGE signaling pathway. These effects could be inhibited by hyperoside. Our findings suggest a novel role for hyperoside in the treatment and prevention of diabetes.

摘要

桃叶珊瑚苷是许多药用植物中的一种主要活性成分,这些植物在传统中药中被用于治疗神经保护、抗炎和抗氧化作用。这些作用的分子机制尚不清楚。在这项研究中,用体外培养的静止型内皮细胞(ECV304)处理晚期糖基化终产物(AGEs),同时存在或不存在桃叶珊瑚苷。结果表明,AGEs 诱导 ECV304 细胞中 c-Jun N 末端激酶(JNK)的激活和凋亡。桃叶珊瑚苷抑制这些作用并促进 ECV304 细胞增殖。此外,桃叶珊瑚苷显著抑制 AGE 刺激的 ECV304 细胞中 RAGE 的表达,而 RAGE 的敲低抑制了 AGE 诱导的 JNK 激活。这些结果表明,AGEs 可能通过 RAGE 信号通路促进 JNK 的激活,从而抑制 ECV304 细胞的活力。这些作用可以被桃叶珊瑚苷抑制。我们的研究结果表明,桃叶珊瑚苷在糖尿病的治疗和预防中有新的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/0ff4c873cbb1/ijms-14-22697f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/e77e272c35b1/ijms-14-22697f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/8bbeeae1b7ea/ijms-14-22697f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/91939874b465/ijms-14-22697f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/81aba6d50470/ijms-14-22697f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/0ff4c873cbb1/ijms-14-22697f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/e77e272c35b1/ijms-14-22697f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/8bbeeae1b7ea/ijms-14-22697f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/91939874b465/ijms-14-22697f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/81aba6d50470/ijms-14-22697f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b50a/3856085/0ff4c873cbb1/ijms-14-22697f5.jpg

相似文献

1
Hyperoside downregulates the receptor for advanced glycation end products (RAGE) and promotes proliferation in ECV304 cells via the c-Jun N-terminal kinases (JNK) pathway following stimulation by advanced glycation end-products in vitro.金丝桃苷通过体外糖基化终产物刺激,通过 c-Jun N-末端激酶(JNK)通路下调晚期糖基化终产物受体(RAGE),并促进 ECV304 细胞增殖。
Int J Mol Sci. 2013 Nov 18;14(11):22697-707. doi: 10.3390/ijms141122697.
2
Osteomeles schwerinae extracts inhibits the binding to receptors of advanced glycation end products and TGF-β1 expression in mesangial cells under diabetic conditions.川西小石积提取物可抑制糖尿病条件下系膜细胞中晚期糖基化终产物受体的结合及转化生长因子-β1的表达。
Phytomedicine. 2016 Apr 15;23(4):388-97. doi: 10.1016/j.phymed.2016.02.005. Epub 2016 Feb 21.
3
Anti-high-mobility group box-1 (HMGB1) mediates the apoptosis of alveolar epithelial cells (AEC) by receptor of advanced glycation end-products (RAGE)/c-Jun N-terminal kinase (JNK) pathway in the rats of crush injuries.高迁移率族蛋白 B1(HMGB1)通过受体晚期糖基化终产物(RAGE)/c-Jun N-末端激酶(JNK)通路介导挤压伤大鼠肺泡上皮细胞(AEC)凋亡。
J Orthop Surg Res. 2022 Jan 15;17(1):20. doi: 10.1186/s13018-021-02903-7.
4
Advanced Glycation End Products Affect Osteoblast Proliferation and Function by Modulating Autophagy Via the Receptor of Advanced Glycation End Products/Raf Protein/Mitogen-activated Protein Kinase/Extracellular Signal-regulated Kinase Kinase/Extracellular Signal-regulated Kinase (RAGE/Raf/MEK/ERK) Pathway.晚期糖基化终末产物通过晚期糖基化终末产物受体/原癌基因丝氨酸/苏氨酸蛋白激酶/丝裂原活化蛋白激酶/细胞外信号调节激酶激酶/细胞外信号调节激酶(RAGE/Raf/MEK/ERK)通路调节自噬,从而影响成骨细胞的增殖和功能。
J Biol Chem. 2015 Nov 20;290(47):28189-28199. doi: 10.1074/jbc.M115.669499. Epub 2015 Oct 15.
5
Advanced glycation end products induce the expression of interleukin-6 and interleukin-8 by receptor for advanced glycation end product-mediated activation of mitogen-activated protein kinases and nuclear factor-κB in human osteoarthritis chondrocytes.糖基化终产物通过糖基化终产物受体介导的丝裂原活化蛋白激酶和核因子-κB 的激活诱导人骨关节炎软骨细胞中白细胞介素-6 和白细胞介素-8 的表达。
Rheumatology (Oxford). 2011 May;50(5):838-51. doi: 10.1093/rheumatology/keq380. Epub 2010 Dec 20.
6
RAGE expression in rhabdomyosarcoma cells results in myogenic differentiation and reduced proliferation, migration, invasiveness, and tumor growth.横纹肌肉瘤细胞中RAGE的表达导致肌源性分化,并降低增殖、迁移、侵袭能力及肿瘤生长。
Am J Pathol. 2007 Sep;171(3):947-61. doi: 10.2353/ajpath.2007.070049. Epub 2007 Jul 19.
7
RAGE modulates myocardial injury consequent to LAD infarction via impact on JNK and STAT signaling in a murine model.在小鼠模型中,晚期糖基化终末产物受体(RAGE)通过影响JNK和STAT信号传导来调节因左前降支梗死所致的心肌损伤。
Am J Physiol Heart Circ Physiol. 2008 Apr;294(4):H1823-32. doi: 10.1152/ajpheart.01210.2007. Epub 2008 Feb 1.
8
S100A9 promotes human lung fibroblast cells activation through receptor for advanced glycation end-product-mediated extracellular-regulated kinase 1/2, mitogen-activated protein-kinase and nuclear factor-κB-dependent pathways.S100A9 通过晚期糖基化终产物受体介导的细胞外调节激酶 1/2、丝裂原活化蛋白激酶和核因子-κB 依赖性途径促进人肺成纤维细胞的激活。
Clin Exp Immunol. 2013 Sep;173(3):523-35. doi: 10.1111/cei.12139.
9
RAGE modulates hypoxia/reoxygenation injury in adult murine cardiomyocytes via JNK and GSK-3beta signaling pathways.RAGE 通过 JNK 和 GSK-3β信号通路调节成年鼠心肌细胞缺氧/复氧损伤。
PLoS One. 2010 Apr 9;5(4):e10092. doi: 10.1371/journal.pone.0010092.
10
Methylglyoxal-Derived Advanced Glycation End Product (AGE4)-Induced Apoptosis Leads to Mitochondrial Dysfunction and Endoplasmic Reticulum Stress through the RAGE/JNK Pathway in Kidney Cells.甲基乙二醛衍生的晚期糖基化终产物(AGE4)诱导的细胞凋亡通过 RAGE/JNK 通路导致肾脏细胞线粒体功能障碍和内质网应激。
Int J Mol Sci. 2021 Jun 18;22(12):6530. doi: 10.3390/ijms22126530.

引用本文的文献

1
Ge-Gen-Qin-Lian decoction alleviates the symptoms of type 2 diabetes mellitus with inflammatory bowel disease via regulating the AGE-RAGE pathway.膈根芩连汤通过调节 AGE-RAGE 通路缓解 2 型糖尿病合并炎症性肠病的症状。
BMC Complement Med Ther. 2024 Jun 10;24(1):225. doi: 10.1186/s12906-024-04526-x.
2
Hyperoside as a Potential Natural Product Targeting Oxidative Stress in Liver Diseases.金丝桃苷作为一种针对肝脏疾病氧化应激的潜在天然产物
Antioxidants (Basel). 2022 Jul 25;11(8):1437. doi: 10.3390/antiox11081437.
3
Influence of In Vitro Human Digestion Simulation on the Phenolics Contents and Biological Activities of the Aqueous Extracts from Turkish Species.

本文引用的文献

1
RAGE-Mediated Inflammation, Type 2 Diabetes, and Diabetic Vascular Complication.RAGE 介导体炎症、2 型糖尿病和糖尿病血管并发症。
Front Endocrinol (Lausanne). 2013 Aug 21;4:105. doi: 10.3389/fendo.2013.00105. eCollection 2013.
2
Advanced glycation end products induce human corneal epithelial cells apoptosis through generation of reactive oxygen species and activation of JNK and p38 MAPK pathways.晚期糖基化终产物通过产生活性氧自由基和激活 JNK 和 p38 MAPK 通路诱导人角膜上皮细胞凋亡。
PLoS One. 2013 Jun 12;8(6):e66781. doi: 10.1371/journal.pone.0066781. Print 2013.
3
Pharmacological evaluation of hyperin for antihyperglycemic activity and effect on lipid profile in diabetic rats.
体外人体消化模拟对土耳其 品种水提物中酚类物质含量和生物活性的影响。
Molecules. 2021 Sep 1;26(17):5322. doi: 10.3390/molecules26175322.
4
L. Regulates Glutathione Redox Stress and Normalizes Ggt1/Anpep Signaling to Alleviate OVX-Induced Kidney Dysfunction.L.调节谷胱甘肽氧化还原应激并使Ggt1/Anpep信号正常化以减轻去势诱导的肾功能障碍。
Front Pharmacol. 2021 Apr 26;12:628651. doi: 10.3389/fphar.2021.628651. eCollection 2021.
5
Advanced Glycation End Products and Risks for Chronic Diseases: Intervening Through Lifestyle Modification.晚期糖基化终末产物与慢性病风险:通过生活方式改变进行干预
Am J Lifestyle Med. 2017 May 15;13(4):384-404. doi: 10.1177/1559827617708991. eCollection 2019 Jul-Aug.
6
Jinmaitong, a Traditional Chinese Compound Prescription, Ameliorates the Streptozocin-Induced Diabetic Peripheral Neuropathy Rats by Increasing Sciatic Nerve IGF-1 and IGF-1R Expression.中药复方金马通通过增加坐骨神经胰岛素样生长因子-1(IGF-1)和胰岛素样生长因子-1受体(IGF-1R)的表达改善链脲佐菌素诱导的糖尿病周围神经病变大鼠。
Front Pharmacol. 2019 Mar 29;10:255. doi: 10.3389/fphar.2019.00255. eCollection 2019.
7
Improvement in Diabetic Retinopathy through Protection against Retinal Apoptosis in Spontaneously Diabetic Torii Rats Mediated by Ethanol Extract of C.K. Schneid.通过保护自发糖尿病 Torii 大鼠的视网膜细胞凋亡改善糖尿病视网膜病变:C.K. Schneid 乙醇提取物的介导作用
Nutrients. 2019 Mar 4;11(3):546. doi: 10.3390/nu11030546.
8
Anti-hypoglycemic and hepatocyte-protective effects of hyperoside from Zanthoxylum bungeanum leaves in mice with high-carbohydrate/high-fat diet and alloxan-induced diabetes.花椒叶中桃叶珊瑚苷对高糖高脂饮食和四氧嘧啶诱导糖尿病小鼠的抗低血糖和保肝作用。
Int J Mol Med. 2018 Jan;41(1):77-86. doi: 10.3892/ijmm.2017.3211. Epub 2017 Oct 25.
9
Hyperglycemia-induced oxidative stress and heart disease-cardioprotective effects of rooibos flavonoids and phenylpyruvic acid-2--β-D-glucoside.高血糖诱导的氧化应激以及南非红叶茶黄酮和苯基丙酮酸-2--β-D-葡萄糖苷对心脏病的心脏保护作用。
Nutr Metab (Lond). 2017 Jul 10;14:45. doi: 10.1186/s12986-017-0200-8. eCollection 2017.
10
Hyperoside inhibits the effects induced by oxidized low-density lipoprotein in vascular smooth muscle cells via oxLDL-LOX-1-ERK pathway.金丝桃苷通过 oxLDL-LOX-1-ERK 通路抑制氧化型低密度脂蛋白诱导的血管平滑肌细胞作用。
Mol Cell Biochem. 2017 Sep;433(1-2):169-176. doi: 10.1007/s11010-017-3025-x. Epub 2017 Apr 22.
金丝桃苷对糖尿病大鼠的降血糖活性及脂质谱影响的药理学评价
Indian J Exp Biol. 2013 Jan;51(1):65-72.
4
Vitamin A (retinol) downregulates the receptor for advanced glycation endproducts (RAGE) by oxidant-dependent activation of p38 MAPK and NF-kB in human lung cancer A549 cells.维生素 A(视黄醇)通过氧化应激依赖性激活 p38MAPK 和 NF-κB 下调人肺癌 A549 细胞中晚期糖基化终产物(RAGE)受体。
Cell Signal. 2013 Apr;25(4):939-54. doi: 10.1016/j.cellsig.2013.01.013. Epub 2013 Jan 16.
5
Simvastatin inhibits the additive activation of ERK1/2 and proliferation of rat vascular smooth muscle cells induced by combined mechanical stress and oxLDL through LOX-1 pathway.辛伐他汀通过 LOX-1 途径抑制机械应力和氧化型低密度脂蛋白联合诱导的大鼠血管平滑肌细胞 ERK1/2 的加性激活和增殖。
Cell Signal. 2013 Jan;25(1):332-40. doi: 10.1016/j.cellsig.2012.10.006. Epub 2012 Oct 13.
6
Hyperoside protects cortical neurons from oxygen-glucose deprivation-reperfusion induced injury via nitric oxide signal pathway.金丝桃苷通过一氧化氮信号通路保护皮质神经元免受氧葡萄糖剥夺再灌注诱导的损伤。
Brain Res. 2012 Aug 21;1469:164-73. doi: 10.1016/j.brainres.2012.06.044. Epub 2012 Jul 4.
7
Panax notogingseng saponins suppress RAGE/MAPK signaling and NF-kappaB activation in apolipoprotein-E-deficient atherosclerosis-prone mice.三七皂苷抑制载脂蛋白E缺乏的动脉粥样硬化易患小鼠中的RAGE/MAPK信号通路和NF-κB激活。
Cell Physiol Biochem. 2012;29(5-6):875-82. doi: 10.1159/000315061. Epub 2012 May 11.
8
RAGE mediates accelerated diabetic vein graft atherosclerosis induced by combined mechanical stress and AGEs via synergistic ERK activation.RAGE 通过协同激活 ERK 介导由机械应力和 AGEs 共同作用引起的糖尿病性静脉移植物动脉粥样硬化加速。
PLoS One. 2012;7(4):e35016. doi: 10.1371/journal.pone.0035016. Epub 2012 Apr 9.
9
Selenium downregulates RAGE and NFκB expression in diabetic rats.硒可下调糖尿病大鼠 RAGE 和 NFκB 的表达。
Biol Trace Elem Res. 2012 Oct;149(1):71-7. doi: 10.1007/s12011-012-9401-1. Epub 2012 Apr 5.
10
Down-regulation of vascular HMGB1 and RAGE expression by n-3 polyunsaturated fatty acids is accompanied by amelioration of chronic vasculopathy of small bowel allografts.n-3 多不饱和脂肪酸可下调血管高迁移率族蛋白 B1 和受体(AGER)的表达,改善小肠移植后慢性血管病变。
J Nutr Biochem. 2012 Oct;23(10):1333-40. doi: 10.1016/j.jnutbio.2011.08.002. Epub 2012 Jan 2.