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莨菪烷类生物碱,从曼陀罗中提取,通过 STAT3/P38/ERK1/2 通路抑制角质形成细胞增殖和咪喹莫特诱导的银屑病样皮炎。

Withanolides, Extracted from Datura Metel L. Inhibit Keratinocyte Proliferation and Imiquimod-Induced Psoriasis-Like Dermatitis via the STAT3/P38/ERK1/2 Pathway.

机构信息

Key Laboratory of Chinese Materia Medica, Heilongjiang University of Chinese Medicine, 24 Heping Road, Xiangfang District, Harbin 150040, China.

School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, 280 Outer Ring Road, University Town, Guangzhou 510006, China.

出版信息

Molecules. 2019 Jul 17;24(14):2596. doi: 10.3390/molecules24142596.

DOI:10.3390/molecules24142596
PMID:31319488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6680890/
Abstract

Psoriasis is an immune-mediated inflammatory dermatosis characterized by epidermal hyperplasia and excessive infiltration of inflammatory cells. Withanolides, extracted from L.; are the main effective components for the treatment of psoriasis. However, the precise mechanisms of action of withanolides for the treatment of psoriasis remain unclear. We found that treatment with withanolides alleviated imiquimod (IMQ)-induced epidermal hyperplasia and inflammatory cell infiltration in the effective skin of model mice. In addition, we also found that withanolides suppressed the activation of STAT3, ERK1/2 and P38 signaling pathways in IMQ-stimulated HaCat cells. These results suggest that withanolides possess an anti-inflammatory effect and have significant therapeutic potential for the prevention and treatment of psoriasis.

摘要

银屑病是一种免疫介导的炎症性皮肤病,其特征是表皮过度增生和炎症细胞过度浸润。 来自 L. 的 withanolides 是治疗银屑病的主要有效成分。 然而,withanolides 治疗银屑病的确切作用机制尚不清楚。 我们发现,withanolides 治疗可减轻咪喹莫特(IMQ)诱导的模型小鼠有效皮肤的表皮过度增生和炎症细胞浸润。 此外,我们还发现 withanolides 抑制了 IMQ 刺激的 HaCat 细胞中 STAT3、ERK1/2 和 P38 信号通路的激活。 这些结果表明,withanolides 具有抗炎作用,对预防和治疗银屑病具有重要的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/81b8a52a3f77/molecules-24-02596-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/9660c5e65b0b/molecules-24-02596-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/2d49ead5aea6/molecules-24-02596-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/065e41c96b23/molecules-24-02596-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/b8534d6a9611/molecules-24-02596-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/4d2a2e02a670/molecules-24-02596-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/5a72920dfe0c/molecules-24-02596-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/7bdfa4eec16f/molecules-24-02596-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/fc88bad918fb/molecules-24-02596-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/81b8a52a3f77/molecules-24-02596-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/9660c5e65b0b/molecules-24-02596-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/2d49ead5aea6/molecules-24-02596-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/065e41c96b23/molecules-24-02596-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/b8534d6a9611/molecules-24-02596-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/4d2a2e02a670/molecules-24-02596-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/5a72920dfe0c/molecules-24-02596-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/7bdfa4eec16f/molecules-24-02596-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/fc88bad918fb/molecules-24-02596-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/6680890/81b8a52a3f77/molecules-24-02596-g009.jpg

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本文引用的文献

1
Selective Immunomodulation of Inflammatory Pathways in Keratinocytes by the Janus Kinase (JAK) Inhibitor Tofacitinib: Implications for the Employment of JAK-Targeting Drugs in Psoriasis.角质形成细胞中 Janus 激酶(JAK)抑制剂托法替尼对炎症途径的选择性免疫调节:在银屑病中应用 JAK 靶向药物的意义。
J Immunol Res. 2018 Nov 19;2018:7897263. doi: 10.1155/2018/7897263. eCollection 2018.
2
Acetyl-11-keto-β-boswellic acid inhibits the secretion of cytokines by dendritic cells via the TLR7/8 pathway in an imiquimod-induced psoriasis mouse model and in vitro.乙酰-11-酮-β-乳香酸通过 TLR7/8 通路抑制咪喹莫特诱导的银屑病小鼠模型和体外树突状细胞细胞因子的分泌。
Life Sci. 2018 Aug 15;207:90-104. doi: 10.1016/j.lfs.2018.05.044. Epub 2018 May 31.
3
Front Oncol. 2021 Apr 26;11:624369. doi: 10.3389/fonc.2021.624369. eCollection 2021.
8-Methoxypsoralen Plus Ultraviolet A Reduces the Psoriatic Response to Imiquimod in a Murine Model.8-甲氧基补骨脂素加紫外线 A 减少咪喹莫特诱导的银屑病样小鼠模型的反应。
Acta Derm Venereol. 2018 Jun 8;98(6):576-584. doi: 10.2340/00015555-2905.
4
Topical Sunitinib ointment alleviates Psoriasis-like inflammation by inhibiting the proliferation and apoptosis of keratinocytes.局部用舒尼替尼软膏通过抑制角质形成细胞的增殖和凋亡来缓解银屑病样炎症。
Eur J Pharmacol. 2018 Apr 5;824:57-63. doi: 10.1016/j.ejphar.2018.01.048. Epub 2018 Jan 31.
5
Scanning the Immunopathogenesis of Psoriasis.扫描银屑病的免疫发病机制。
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6
Anti-psoriatic and toxicity evaluation of methotrexate loaded chitin nanogel in imiquimod induced mice model.载甲氨蝶呤壳聚糖纳米凝胶在咪喹莫特诱导的小鼠模型中的抗银屑病和毒性评价。
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7
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8
Imiquimod-induced psoriasis-like inflammation in differentiated Human keratinocytes: Its evaluation using curcumin.咪喹莫特诱导分化的人角质形成细胞银屑病样炎症:姜黄素的评价。
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9
Withasteroid B from D. metel L. regulates immune responses by modulating the JAK/STAT pathway and the IL-17 RORγt /IL-10 FoxP3 ratio.曼陀罗中的Withasteroid B通过调节JAK/STAT信号通路以及IL-17 RORγt /IL-10 FoxP3比值来调控免疫反应。
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10
Imiquimod has strain-dependent effects in mice and does not uniquely model human psoriasis.咪喹莫特在小鼠中具有菌株依赖性效应,并非唯一能模拟人类银屑病的模型。
Genome Med. 2017 Mar 9;9(1):24. doi: 10.1186/s13073-017-0415-3.