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本文引用的文献

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ERK1 and ERK2 Map Kinases: Specific Roles or Functional Redundancy?ERK1 和 ERK2 丝裂原活化蛋白激酶:特定作用还是功能冗余?
Front Cell Dev Biol. 2016 Jun 8;4:53. doi: 10.3389/fcell.2016.00053. eCollection 2016.
2
Synergistic Effect of Compounds from a Chinese Herb: Compatibility and Dose Optimization of Compounds from N-Butanol Extract of Ipomoea stolonifera.一种中草药中化合物的协同作用:茑萝正丁醇提取物中化合物的配伍及剂量优化
Sci Rep. 2016 Jun 3;6:27014. doi: 10.1038/srep27014.
3
Review: The Lacrimal Gland and Its Role in Dry Eye.综述:泪腺及其在干眼中的作用。
J Ophthalmol. 2016;2016:7542929. doi: 10.1155/2016/7542929. Epub 2016 Mar 2.
4
Esculetin Inhibits VEGF-Induced Angiogenesis Both In Vitro and In Vivo.七叶亭在体内外均可抑制血管内皮生长因子诱导的血管生成。
Am J Chin Med. 2016;44(1):61-76. doi: 10.1142/S0192415X1650004X.
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Esculetin induces apoptosis in human colon cancer cells by inducing endoplasmic reticulum stress.七叶亭通过诱导内质网应激诱导人结肠癌细胞凋亡。
Cell Biochem Funct. 2015 Oct;33(7):487-94. doi: 10.1002/cbf.3146. Epub 2015 Oct 5.
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HIF-prolyl hydroxylase is a potential molecular target for esculetin-mediated anti-colitic effects.缺氧诱导因子脯氨酰羟化酶是七叶亭介导的抗结肠炎作用的潜在分子靶点。
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Pathway activation profiling reveals new insights into age-related macular degeneration and provides avenues for therapeutic interventions.通路激活分析揭示了与年龄相关性黄斑变性的新见解,并为治疗干预提供了途径。
Aging (Albany NY). 2014 Dec;6(12):1064-75. doi: 10.18632/aging.100711.
9
Esculetin, a coumarin derivative, exerts in vitro and in vivo antiproliferative activity against hepatocellular carcinoma by initiating a mitochondrial-dependent apoptosis pathway.七叶亭,一种香豆素衍生物,通过启动线粒体依赖性凋亡途径,对肝癌细胞发挥体内外抗增殖活性。
Braz J Med Biol Res. 2015 Mar;48(3):245-53. doi: 10.1590/1414-431X20144074. Epub 2014 Dec 12.
10
Managing Sjögren's Syndrome and non-Sjögren Syndrome dry eye with anti-inflammatory therapy.采用抗炎疗法治疗干燥综合征和非干燥综合征性干眼
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七叶亭局部给药作为实验性干眼症综合征的一种潜在治疗方法。

Topical administration of Esculetin as a potential therapy for experimental dry eye syndrome.

作者信息

Jiang D, Liu X, Hu J

机构信息

Department of Ophthalmology, Longhua Hosptial, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Eye (Lond). 2017 Dec;31(12):1724-1732. doi: 10.1038/eye.2017.117. Epub 2017 Jun 23.

DOI:10.1038/eye.2017.117
PMID:28643798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5733282/
Abstract

PurposeIn this study, we investigated the therapeutic effects of topical Esculetin for dry eye rabbits through the ocular tests, inflammatory factor levels and specific phosphorylated protein expressions of ERK1/2 singnal pathway.Patients and methodsThirty-two healthy adult male New Zealand white rabbits were chosen for the study. DES models were established after removing of the main lacrimal gland, Harderian gland and nictitating membrane in the left eyes and randomly divided into group DES control, group CsA, group Esculetin and group Esculetin combined with CsA (C&E), meanwhile the right eyes served as group Normal control. Schirmer's I tests, fluorescein scores, goblet cell densities, inflammatory cytokines IL-1α,IL-1β,TNF-αlevels were observed by slit-lamp microscope, conjunctival impression cytology and ELISA essay at week 0, 1, 2, 4, 8. Phosphorylated-ERK1/2 expressions were detected in Western blot analysis at week 8.ResultsAfter induction of DES, aqueous tear production and goblet cell density were decreased, FL score was much higher in group DES control throughout the study (P<0.05). Both topical Esculetin and Esculetin combing CsA increased the SIT values (10±1 mm, 14±3 mm, P<0.05) and goblet cell densities (77±12/HP, 92±12/HP, P<0.05), decreased FL scores (7.48±0.33, 5.09±0.24, P<0.05) at week 8. Alternations of IL-1α,IL-1β,TNF-αlevels had similar trend. In Western blot analysis, downregulations of p-ERK1/2 were observed in therapy groups when compared with group DES control and the most decreasing was found in group C&E (P<0.05).ConclusionTopical Esculetin improved DES symptoms, downregulated the inflammatory cytokine expressions, suppressed the ERK1/2 pathway and enhanced the therapeutic effect of CsA.

摘要

目的

在本研究中,我们通过眼部测试、炎症因子水平以及ERK1/2信号通路特定磷酸化蛋白表达,研究了局部应用七叶亭对干眼兔的治疗效果。

患者和方法

选择32只健康成年雄性新西兰白兔进行研究。在切除左眼的主泪腺、哈德氏腺和瞬膜后建立干眼模型,并随机分为干眼对照组、环孢素A组、七叶亭组和七叶亭联合环孢素A组(C&E),同时将右眼作为正常对照组。在第0、1、2、4、8周通过裂隙灯显微镜、结膜印迹细胞学检查和酶联免疫吸附测定法观察泪液分泌试验、荧光素评分、杯状细胞密度、炎症细胞因子IL-1α、IL-1β、TNF-α水平。在第8周通过蛋白质印迹分析检测磷酸化ERK1/2的表达。

结果

诱导干眼后,泪液分泌量和杯状细胞密度降低,在整个研究过程中干眼对照组的荧光素评分高得多(P<0.05)。局部应用七叶亭和七叶亭联合环孢素A均提高了第8周的泪液分泌试验值(10±1毫米,14±3毫米,P<0.05)和杯状细胞密度(77±12/HP,92±12/HP,P<0.05),降低了荧光素评分(7.48±0.33,5.09±0.24,P<0.05)。IL-1α、IL-1β、TNF-α水平的变化趋势相似。在蛋白质印迹分析中,与干眼对照组相比,治疗组中观察到磷酸化ERK1/2下调,且在C&E组中下降最为明显(P<0.05)。

结论

局部应用七叶亭改善了干眼症状,下调了炎症细胞因子表达,抑制了ERK1/2通路,并增强了环孢素A的治疗效果。