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清鹏软膏通过改善实验性变应性接触性皮炎中的炎症反应及瘙痒相关分子的失调发挥止痒作用。

Qingpeng Ointment Ameliorates Inflammatory Responses and Dysregulation of Itch-Related Molecules for Its Antipruritic Effects in Experimental Allergic Contact Dermatitis.

作者信息

Gong Xuan, Xiong Hui, Liu Sisi, Liu Yutong, Yin Liang, Tu Chuyue, Wang Hua, Zhao Zhongqiu, Chen Weiwu, Mei Zhinan

机构信息

School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan, China.

College of Life Science, South-Central University for Nationalities, Wuhan, China.

出版信息

Front Pharmacol. 2019 Apr 9;10:354. doi: 10.3389/fphar.2019.00354. eCollection 2019.

Abstract

The pathogenesis of itchy skin diseases including allergic contact dermatitis (ACD) is complicated and the treatment of chronic itch is a worldwide problem. One traditional Tibetan medicine, Qingpeng ointment (QP), has been used in treatment of ACD in China for years. In this study we used HPLC and LC/MS analysis, combined with a BATMAN-TCM platform, for detailed HPLC fingerprint analysis and network pharmacology of QP, and investigated the anti-inflammatory and antipruritic activities of QP on ACD induced by squaric acid dibutylester (SADBE) in mice. The BATMAN-TCM analysis provided information of effector molecules of the main ingredients of QP, and possible chronic dermatitis-associated molecules and cell signaling pathways by QP. In ACD mice, QP treatment suppressed the scratching behavior induced by SADBE in a dose-dependent manner and inhibited the production of Th1/2 cytokines in serum and spleen. Also, QP treatment reversed the upregulation of mRNAs levels of itch-related genes in the skin (TRPV4, TSLP, GRP, and MrgprA3) and DRGs (TRPV1, TRPA1, GRP, and MrgprA3). Furthermore, QP suppressed the phosphorylation of Erk and p38 in the skin. In all, our work indicated that QP can significantly attenuate the pathological alterations of Th1/2 cytokines and itch-related mediators, and inhibit the phosphorylation of MAPKs to treat the chronic itch.

摘要

包括过敏性接触性皮炎(ACD)在内的瘙痒性皮肤病的发病机制复杂,慢性瘙痒的治疗是一个全球性问题。一种传统藏药青鹏软膏(QP)在中国已用于治疗ACD多年。在本研究中,我们采用高效液相色谱(HPLC)和液相色谱/质谱(LC/MS)分析,并结合中药系统药理学数据库与分析平台(BATMAN-TCM),对QP进行详细的HPLC指纹图谱分析和网络药理学研究,并研究QP对二丁基环丁烯四羧酸(SADBE)诱导的小鼠ACD的抗炎和止痒活性。BATMAN-TCM分析提供了QP主要成分的效应分子信息,以及QP可能涉及的慢性皮炎相关分子和细胞信号通路信息。在ACD小鼠中,QP治疗以剂量依赖性方式抑制SADBE诱导的搔抓行为,并抑制血清和脾脏中Th1/2细胞因子的产生。此外,QP治疗逆转了皮肤(瞬时受体电位香草酸亚型4(TRPV4)、胸腺基质淋巴细胞生成素(TSLP)、胃泌素释放肽(GRP)和 Mas相关G蛋白偶联受体A3(MrgprA3))和背根神经节(TRPV1、瞬时受体电位锚蛋白1(TRPA1)、GRP和MrgprA3)中瘙痒相关基因mRNA水平的上调。此外,QP抑制皮肤中细胞外信号调节激酶(Erk)和p38的磷酸化。总之,我们的研究表明,QP可显著减轻Th1/2细胞因子和瘙痒相关介质的病理改变,并抑制丝裂原活化蛋白激酶(MAPKs)的磷酸化,从而治疗慢性瘙痒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/010f/6465648/9b53ae08c02e/fphar-10-00354-g001.jpg

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