Ethanol extract of Herpetospermum caudigerum Wall ameliorates psoriasis-like skin inflammation and promotes degradation of keratinocyte-derived ICAM-1 and CXCL9

IF 4.2 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE
Ya Zhong , Bo-wen Zhang , Jin-tao Li , Xin Zeng , Jun-xia Pei , Ya-mei Zhang , Yi-xi Yang , Fu-lun Li , Yu Deng , Qi Zhao
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引用次数: 0

Abstract

Objective

To explore whether the ethanol extract of Herpetospermum caudigerum Wall (EHC), a Xizang medicinal plant traditionally used for treating liver diseases, can improve imiquimod-induced psoriasis-like skin inflammation.

Methods

Immunohistochemistry and immunofluorescence staining were used to determine the effects of topical EHC use in vivo on the skin pathology of imiquimod-induced psoriasis in mice. The protein levels of interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α), and interleukin-17A (IL-17A) in mouse skin samples were examined using immunohistochemical staining. In vitro, IFN-γ-induced HaCaT cells with or without EHC treatment were used to evaluate the expression of keratinocyte-derived intercellular cell adhesion molecule-1 (ICAM-1) and chemokine CXC ligand 9 (CXCL9) using Western blotting and reverse transcription-quantitative polymerase chain reaction. The protein synthesis inhibitor cycloheximide and proteasome inhibitor MG132 were utilized to validate the EHC-mediated mechanism underlying degradation of ICAM-1 and CXCL9.

Results

EHC improved inflammation in the imiquimod-induced psoriasis mouse model and reduced the levels of IFN-γ, TNF-α, and IL-17A in psoriatic lesions. Treatment with EHC also suppressed ICAM-1 and CXCL9 in epidermal keratinocytes. Further mechanistic studies revealed that EHC suppressed keratinocyte-derived ICAM-1 and CXCL9 by promoting ubiquitin–proteasome-mediated protein degradation rather than transcriptional repression. Seven primary compounds including ehletianol C, dehydrodiconiferyl alcohol, herpetrione, herpetin, herpetotriol, herpetetrone and herpetetrol were identified from the EHC using ultra-performance liquid chromatography-quadrupole-time of flight-mass spectrometry.

Conclusion

Topical application of EHC ameliorates psoriasis-like skin symptoms and improves the inflammation at the lesion sites.

Please cite this article as: Zhong Y, Zhang BW, Li JT, Zeng X, Pei JX, Zhang YM, Yang YX, Li FL, Deng Y, Zhao Q. Ethanol extract of Herpetospermum caudigerum Wall ameliorates psoriasis-like skin inflammation and promotes degradation of keratinocyte-derived ICAM-1 and CXCL9. J Integr Med. 2023; 21(6): 584–592.

蜈蚣草乙醇提取物改善牛皮癣样皮肤炎症,促进角化细胞来源的ICAM-1和CXCL9的降解
目的探讨西藏省治疗肝脏疾病的药用植物蜈蚣草(Herpetospermum caudigerum Wall, EHC)乙醇提取物对吡喹莫德诱导的银屑病样皮肤炎症的改善作用。方法采用免疫组织化学和免疫荧光染色法观察体外外用EHC对吡喹莫德致银屑病小鼠皮肤病理的影响。采用免疫组化染色法检测小鼠皮肤样品中干扰素-γ (IFN-γ)、肿瘤坏死因子-α (TNF-α)、白细胞介素- 17a (IL-17A)蛋白水平。在体外,使用IFN-γ诱导的HaCaT细胞,通过Western blotting和逆转录-定量聚合酶链反应,评估角化细胞来源的细胞间细胞粘附分子-1 (ICAM-1)和趋化因子CXC配体9 (CXCL9)的表达。利用蛋白质合成抑制剂环己亚胺和蛋白酶体抑制剂MG132验证ehc介导的ICAM-1和CXCL9降解机制。结果hcs改善了吡喹莫德诱导的银屑病小鼠模型的炎症反应,降低了银屑病皮损中IFN-γ、TNF-α和IL-17A的水平。EHC也抑制了表皮角质形成细胞中的ICAM-1和CXCL9。进一步的机制研究表明,EHC通过促进泛素蛋白酶体介导的蛋白质降解而不是转录抑制来抑制角化细胞来源的ICAM-1和CXCL9。采用超高效液相色谱-四极杆飞行时间质谱法从EHC中鉴定出7个主要化合物,分别为乙烯醇C、脱氢二龙脑醇、herpetrione、herpetin、herpetotriol、herpetetrone和herpetetrol。结论局部应用EHC可改善银屑病样皮肤症状,改善病变部位的炎症反应。钟毅,张宝文,李金涛,曾鑫,裴建新,张彦明,杨云云,李方飞,邓勇,赵强。荆芥壁乙醇提取物改善银屑病样皮肤炎症,促进角化细胞来源的ICAM-1和CXCL9的降解。中华医学杂志;2009;21(6): 584 - 592。
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来源期刊
Journal of Integrative Medicine-Jim
Journal of Integrative Medicine-Jim Medicine-Complementary and Alternative Medicine
CiteScore
9.20
自引率
4.20%
发文量
3319
期刊介绍: The predecessor of JIM is the Journal of Chinese Integrative Medicine (Zhong Xi Yi Jie He Xue Bao). With this new, English-language publication, we are committed to make JIM an international platform for publishing high-quality papers on complementary and alternative medicine (CAM) and an open forum in which the different professions and international scholarly communities can exchange views, share research and their clinical experience, discuss CAM education, and confer about issues and problems in our various disciplines and in CAM as a whole in order to promote integrative medicine. JIM is indexed/abstracted in: MEDLINE/PubMed, ScienceDirect, Emerging Sources Citation Index (ESCI), Scopus, Embase, Chemical Abstracts (CA), CAB Abstracts, EBSCO, WPRIM, JST China, Chinese Science Citation Database (CSCD), and China National Knowledge Infrastructure (CNKI). JIM Editorial Office uses ThomsonReuters ScholarOne Manuscripts as submitting and review system (submission link: http://mc03.manuscriptcentral.com/jcim-en). JIM is published bimonthly. Manuscripts submitted to JIM should be written in English. Article types include but are not limited to randomized controlled and pragmatic trials, translational and patient-centered effectiveness outcome studies, case series and reports, clinical trial protocols, preclinical and basic science studies, systematic reviews and meta-analyses, papers on methodology and CAM history or education, conference proceedings, editorials, commentaries, short communications, book reviews, and letters to the editor. Our purpose is to publish a prestigious international journal for studies in integrative medicine. To achieve this aim, we seek to publish high-quality papers on any aspects of integrative medicine, such as acupuncture and traditional Chinese medicine, Ayurveda medicine, herbal medicine, homeopathy, nutrition, chiropractic, mind-body medicine, taichi, qigong, meditation, and any other modalities of CAM; our commitment to international scope ensures that research and progress from all regions of the world are widely covered. These ensure that articles published in JIM have the maximum exposure to the international scholarly community. JIM can help its authors let their papers reach the widest possible range of readers, and let all those who share an interest in their research field be concerned with their study.
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