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在咪喹莫特诱导的银屑病样小鼠模型中使用桃丹颗粒减轻银屑病性皮炎机制的转录组学分析

Transcriptomic Analysis of the Mechanisms for Alleviating Psoriatic Dermatitis Using Taodan Granules in an Imiquimod-Induced Psoriasis-like Mouse Model.

作者信息

Kuai Le, Luo Ying, Qu Keshen, Ru Yi, Luo Yue, Ding Xiaojie, Xing Meng, Liu Liu, Sun Xiaoying, Li Xin, Li Bin

机构信息

Department of Dermatology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Institute of Dermatology, Shanghai Academy of Traditional Chinese Medicine, Shanghai, China.

出版信息

Front Pharmacol. 2021 Apr 14;12:632414. doi: 10.3389/fphar.2021.632414. eCollection 2021.

DOI:10.3389/fphar.2021.632414
PMID:33995034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8114823/
Abstract

Taodan granules (TDGs) are clinically efficacious for treating psoriasis, buttheir specific mechanisms of action are unclear. In this study, we determined the concentrations of tanshinone IIA and curcumol using high-performance liquid chromatography (HPLC) to establish quality control parameters for assessing the mechanism of TDGs in treating psoriasis. Thereafter, a mouse model of psoriasis was treated with TDGs. TDGs attenuated imiquimod-induced typical erythema, scales, and thickening of the back and ear lesions in the psoriatic mouse model. Furthermore, PCNA and Ki67-positive cells were reduced in the of psoriatic lesions following TDG treatment. Finally, the sequencing results were verified using a multitude of methods, and the mechanism of action of TDGs against psoriasis was found to be via the upregulation of metabolic signaling pathways such as the Gly-Ser-Thr axis, the downregulation of immune and inflammatory pathways, and the decrease in Rac2 and Arhgdib concentrations. Overall, this study clarified the mechanism of TDG treatment for psoriasis and provided evidence for its clinical application.

摘要

桃丹颗粒(TDGs)在临床上对治疗银屑病有效,但其具体作用机制尚不清楚。在本研究中,我们使用高效液相色谱法(HPLC)测定丹参酮IIA和莪术醇的浓度,以建立评估TDGs治疗银屑病机制的质量控制参数。此后,用TDGs治疗银屑病小鼠模型。TDGs减轻了咪喹莫特诱导的银屑病小鼠模型背部和耳部病变的典型红斑、鳞屑和增厚。此外,TDG治疗后银屑病病变处PCNA和Ki67阳性细胞减少。最后,通过多种方法验证测序结果,发现TDGs抗银屑病的作用机制是通过上调Gly-Ser-Thr轴等代谢信号通路、下调免疫和炎症通路以及降低Rac2和Arhgdib浓度。总体而言,本研究阐明了TDG治疗银屑病的机制,并为其临床应用提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64a3/8114823/9f453c90521b/fphar-12-632414-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64a3/8114823/c1a2ed67d23e/fphar-12-632414-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64a3/8114823/47da04e98ed2/fphar-12-632414-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64a3/8114823/58adcbbf82e4/fphar-12-632414-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64a3/8114823/9f453c90521b/fphar-12-632414-g005.jpg

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