• 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

槲皮素-3-O-(2″-没食子酸酯)-α-L-鼠李糖苷局部应用对NC/Nga小鼠特应性皮炎的影响。

Effect of topical application of quercetin-3-O-(2″-gallate)-α-l-rhamnopyranoside on atopic dermatitis in NC/Nga mice.

作者信息

Park Eun Joo, Kim Ji-Yun, Jeong Mi Sook, Park Kui Young, Park Kwan Hee, Lee Min Won, Joo Seong Soo, Seo Seong Jun

机构信息

College of Medicine, Department of Dermatology, Hallym University College of Medicine, Anyang, South Korea.

Institute of Atopic Dermatitis, Department of Dermatology, Chung-Ang University College of Medicine, Seoul, South Korea.

出版信息

J Dermatol Sci. 2015 Mar;77(3):166-72. doi: 10.1016/j.jdermsci.2014.12.005. Epub 2015 Jan 3.

DOI:10.1016/j.jdermsci.2014.12.005
PMID:25617237
Abstract

BACKGROUND

Quercetin-3-O-(2″-gallate)-α-l-rhamnopyranoside (QGR) is a new quercetin derivative which is isolated from the leaves of Acer ginnala Maxim, a native plant of Korea. Quercetin has several biological effects including antioxidative, anti-inflammatory, and anti-allergic effects. However, the topical effect of QGR on atopic dermatitis (AD) like skin lesion in NC/Nga mice has not been studied.

OBJECTIVE

To evaluate the anti-inflammatory and anti-allergic effect of QGR in a murine model of atopic dermatitis.

METHODS

We measured inducible nitric oxide synthase (iNOS) and cyclooxygenase -2(COX-2) level in RAW264.7 cell with QGR treatment. And after induction of AD like skin lesions with Dermatophagoides farina (Df) ointment, mice were treated with QGR and control drugs. Clinical scores, interleukin (IL) 4, 5, and 13, serum IgE, eosinophil levels, iNOS and COX-2 level were evaluated.

RESULTS

Results show that mRNA level of iNOS and COX-2 in vitro were decreased after QGR treatment. Topical QGR markedly decreased the iNOS and COX-2 mRNA expressions in the skin. QGR also significantly suppressed the increase in the level of total plasma IgE and eosinophils. In addition, topical application of QGR down-regulated the expressions of the cytokines, IL-4,5 and 13, which were induced by Df ointment stimulation.

CONCLUSIONS

In the present study, we showed that topical application of QGR ameliorated Df-induced AD-like inflammatory responses in NC/Nga mice. These results demonstrate that QGR might be beneficial in the treatment of AD.

摘要

背景

槲皮素-3-O-(2″-没食子酸酯)-α-L-鼠李糖苷(QGR)是一种新的槲皮素衍生物,从韩国本土植物茶条槭的叶子中分离得到。槲皮素具有多种生物学效应,包括抗氧化、抗炎和抗过敏作用。然而,QGR对NC/Nga小鼠特应性皮炎(AD)样皮肤损伤的局部作用尚未得到研究。

目的

评估QGR在特应性皮炎小鼠模型中的抗炎和抗过敏作用。

方法

我们用QGR处理RAW264.7细胞,检测诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)水平。在用粉尘螨(Df)软膏诱导AD样皮肤损伤后,用QGR和对照药物处理小鼠。评估临床评分、白细胞介素(IL)4、5和13、血清IgE、嗜酸性粒细胞水平、iNOS和COX-2水平。

结果

结果显示,QGR处理后体外iNOS和COX-2的mRNA水平降低。局部应用QGR显著降低皮肤中iNOS和COX-2的mRNA表达。QGR还显著抑制了总血浆IgE水平和嗜酸性粒细胞的增加。此外,局部应用QGR下调了由Df软膏刺激诱导的细胞因子IL-4、5和13的表达。

结论

在本研究中,我们表明局部应用QGR可改善Df诱导的NC/Nga小鼠AD样炎症反应。这些结果表明QGR可能对AD的治疗有益。

相似文献

1
Effect of topical application of quercetin-3-O-(2″-gallate)-α-l-rhamnopyranoside on atopic dermatitis in NC/Nga mice.槲皮素-3-O-(2″-没食子酸酯)-α-L-鼠李糖苷局部应用对NC/Nga小鼠特应性皮炎的影响。
J Dermatol Sci. 2015 Mar;77(3):166-72. doi: 10.1016/j.jdermsci.2014.12.005. Epub 2015 Jan 3.
2
Effect of taxifolin glycoside on atopic dermatitis-like skin lesions in NC/Nga mice.金雀异黄素糖苷对 NC/Nga 小鼠特应性皮炎样皮肤损伤的影响。
Phytother Res. 2010 Jul;24(7):1071-7. doi: 10.1002/ptr.3084.
3
Effect of topical application and intraperitoneal injection of oregonin on atopic dermatitis in NC/Nga mice.虎杖苷经皮给药和腹腔注射对 NC/Nga 小鼠特应性皮炎的影响。
Exp Dermatol. 2010 Aug;19(8):e37-43. doi: 10.1111/j.1600-0625.2009.00961.x.
4
Mechanism underlying the effect of combined therapy using glucosamine and low-dose cyclosporine A on the development of atopic dermatitis-like skin lesions in NC/Nga mice.联合使用氨基葡萄糖和低剂量环孢素 A 治疗对 NC/Nga 小鼠特应性皮炎样皮肤损伤发展的作用机制。
Int Immunopharmacol. 2013 Feb;15(2):424-32. doi: 10.1016/j.intimp.2013.01.005. Epub 2013 Jan 22.
5
Therapeutic effects of combination using glucosamine plus tacrolimus (FK-506) on the development of atopic dermatitis-like skin lesions in NC/Nga mice.联合使用氨基葡萄糖加他克莫司(FK-506)治疗 NC/Nga 小鼠特应性皮炎样皮肤损伤的疗效。
Scand J Immunol. 2012 May;75(5):471-8. doi: 10.1111/j.1365-3083.2011.02659.x.
6
A novel atopic dermatitis model induced by topical application with dermatophagoides farinae extract in NC/Nga mice.通过在NC/Nga小鼠局部应用粉尘螨提取物诱导的新型特应性皮炎模型。
Allergol Int. 2007 Jun;56(2):139-48. doi: 10.2332/allergolint.O-06-458. Epub 2007 May 1.
7
In vivo assessment of the effect of taxifolin glycoside on atopic dermatitis-like skin lesions using biomedical tools in NC/Nga mice.使用生物医学工具在NC/Nga小鼠体内评估紫杉叶素糖苷对特应性皮炎样皮肤损伤的影响。
Clin Exp Dermatol. 2015 Jul;40(5):547-55. doi: 10.1111/ced.12522. Epub 2014 Dec 5.
8
Tat peptide-admixed elastic liposomal formulation of hirsutenone for the treatment of atopic dermatitis in NC/Nga mice.混合 Tat 肽的贺尔蒙弹性脂质体配方治疗 NC/Nga 小鼠异位性皮肤炎。
Int J Nanomedicine. 2011;6:2459-67. doi: 10.2147/IJN.S24350. Epub 2011 Oct 20.
9
Modulation of HMGB1 translocation and RAGE/NFκB cascade by quercetin treatment mitigates atopic dermatitis in NC/Nga transgenic mice.槲皮素治疗对HMGB1易位及RAGE/NFκB级联反应的调节作用减轻了NC/Nga转基因小鼠的特应性皮炎。
Exp Dermatol. 2015 Jun;24(6):418-23. doi: 10.1111/exd.12685. Epub 2015 Mar 25.
10
Topical application of two condensed tannins from the root of Rosa multiflora Thunberg for the treatment of atopic dermatitis (AD) in NC/Nga mice.从多花蔷薇根中提取的两种缩合单宁用于治疗 NC/Nga 小鼠特应性皮炎(AD)的局部应用。
Phytother Res. 2011 Oct;25(10):1564-9. doi: 10.1002/ptr.3578. Epub 2011 Jun 30.

引用本文的文献

1
Role of Oxidative Stress and Antioxidants in the Course of Atopic Dermatitis.氧化应激与抗氧化剂在特应性皮炎病程中的作用
Int J Mol Sci. 2025 Apr 29;26(9):4210. doi: 10.3390/ijms26094210.
2
Inhibitory effect of Sanguisorba hakusanensis Makino ethanol extract on atopic dermatitis-like responses in NC/Nga mice and human keratinocytes.地榆日本变种乙醇提取物对 NC/Nga 小鼠和人角质形成细胞特应性皮炎样反应的抑制作用。
Sci Rep. 2023 Sep 5;13(1):14594. doi: 10.1038/s41598-023-41676-3.
3
Antioxidant Activity of Quercetin-Containing Liposomes-in-Gel and Its Effect on Prevention and Treatment of Cutaneous Eczema.
含槲皮素脂质体凝胶的抗氧化活性及其对皮肤湿疹防治的作用
Pharmaceuticals (Basel). 2023 Aug 21;16(8):1184. doi: 10.3390/ph16081184.
4
Outlook on Chronic Venous Disease Treatment: Phytochemical Screening, In Vitro Antioxidant Activity and In Silico Studies for Three Vegetal Extracts.展望慢性静脉疾病的治疗:三种植物提取物的植物化学成分筛选、体外抗氧化活性和计算机模拟研究。
Molecules. 2023 Apr 23;28(9):3668. doi: 10.3390/molecules28093668.
5
Quercetin Improves Inflammation, Oxidative Stress, and Impaired Wound Healing in Atopic Dermatitis Model of Human Keratinocytes.槲皮素可改善特应性皮炎模型中人类角质形成细胞的炎症、氧化应激和受损的伤口愈合。
Pediatr Allergy Immunol Pulmonol. 2020 Jun;33(2):69-79. doi: 10.1089/ped.2019.1137. Epub 2020 May 21.
6
Chemical Composition of a Novel Distillate from Fermented Mixture of Nine Anti-Inflammatory Herbs and Its UVB-Protective Efficacy in Mouse Dorsal Skin via Attenuating Collagen Disruption and Inflammation.一种新型发酵抗炎草药混合物馏分的化学成分及其通过减轻胶原破坏和炎症反应增强 UVB 防护功效在小鼠背部皮肤中的作用。
Molecules. 2020 Dec 29;26(1):124. doi: 10.3390/molecules26010124.
7
Saponin from Schltr Mitigates Oxazolone-Induced Atopic Dermatitis via Modulating Macrophage Activation.Schltr 中的三萜皂苷通过调节巨噬细胞活化缓解了恶唑酮诱导的特应性皮炎。
Mediators Inflamm. 2020 Oct 15;2020:4346367. doi: 10.1155/2020/4346367. eCollection 2020.
8
Topical Application of Extract Rich in Chlorogenic Acid and Rutin Reduces UVB-Induced Skin Damage via Attenuating Collagen Disruption in Mice.富含绿原酸和芦丁的提取物经局部应用可减少 UVB 诱导的皮肤损伤,其机制与减轻胶原破坏有关。
Molecules. 2020 Oct 7;25(19):4577. doi: 10.3390/molecules25194577.
9
Quercetin with the potential effect on allergic diseases.槲皮素对过敏性疾病具有潜在作用。
Allergy Asthma Clin Immunol. 2020 May 14;16:36. doi: 10.1186/s13223-020-00434-0. eCollection 2020.
10
Extract Protects Mouse Skin from UVB Radiation via Attenuating Collagen Disruption and Inflammation.提取物通过减轻胶原蛋白破坏和炎症来保护小鼠皮肤免受 UVB 辐射。
Int J Mol Sci. 2019 Mar 21;20(6):1435. doi: 10.3390/ijms20061435.