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构树通过调节TLR4/NF-κB和PI3K/AKT信号通路改善咪喹莫特诱导的小鼠银屑病样皮肤炎症。

Broussonetia papyrifera ameliorates imiquimod-induced psoriasis-like skin inflammation in mice by modulating the TLR4/NF-κB and PI3K/AKT signaling pathways.

作者信息

Huang Xiaoqiang, Wang Li, Ma Xiaoying, Liu Shunhe, Zhao Hongchang, Zhang Pengbo, Li Liyan, Zhao Wanli, Jia An

机构信息

School of Medicine, Huanghe Science & Technology University, Zhengzhou, China.

School of Pharmacy, Henan University, Kaifeng, China.

出版信息

PLoS One. 2025 May 7;20(5):e0322710. doi: 10.1371/journal.pone.0322710. eCollection 2025.


DOI:10.1371/journal.pone.0322710
PMID:40333872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12057870/
Abstract

Psoriasis is a chronic, immune-mediated inflammatory skin disease, and the inflammatory response plays an important role in its development and progression. Psoriasis can appear at any age and occurs around the world. The pathogenesis of psoriasis has not been fully elucidated, and there is currently no effective treatment method in clinical practice. Broussonetia papyrifera is a traditional Chinese medicine that exhibited a significant therapeutic effect on psoriasis in our previous study due to its remarkable anti-inflammatory and anti-oxidant properties. However, its mechanism of action in treating psoriasis is still unclear. The purpose of this study is to evaluate the anti-psoriasis effect of the B. papyrifera leaves extract (PLE) in vivo and to explore its potential effects. PLE effectively alleviated imiquimod (IMQ)-induced psoriasis-like lesions, reduced psoriasis lesion area and severity index, decreased epidermal hyperplasia, ameliorated the oxidative stress-induced changes in the levels of superoxide dismutase (SOD) and malondialdehyde (MDA), and reduced the levels of the inflammatory cytokines TNF-α and IL-17A. PLE can also reduce the protein expression levels of TLR4, MyD88, p-NF-κBp65, p-IκBα, p-PI3K and p-AKT induced by IMQ model. Our findings suggest that PLE is effective in improving psoriasis-like symptoms, which might be ascribed to the inhibition of the TLR4/NF-κB and PI3K/AKT inflammation pathway. Our study demonstrates the potential mechanism of a natural source of PLE for the treatment of psoriasis. However, it is important to note that these findings lack clinical validation, and further studies are required to validate these results in clinical settings. Additionally, PLE shows potential in being a cost-effective alternative compared to existing biologics, which could have broader implications for psoriasis treatment in the future.

摘要

银屑病是一种慢性、免疫介导的炎症性皮肤病,炎症反应在其发生和发展过程中起着重要作用。银屑病可发生于任何年龄,在世界各地均有出现。银屑病的发病机制尚未完全阐明,目前临床实践中尚无有效的治疗方法。构树是一种传统中药,在我们之前的研究中,因其具有显著的抗炎和抗氧化特性,对银屑病显示出显著的治疗效果。然而,其治疗银屑病的作用机制仍不清楚。本研究的目的是评估构树叶提取物(PLE)在体内的抗银屑病效果,并探索其潜在作用。PLE有效减轻了咪喹莫特(IMQ)诱导的银屑病样病变,降低了银屑病病变面积和严重程度指数,减少了表皮增生,改善了氧化应激诱导的超氧化物歧化酶(SOD)和丙二醛(MDA)水平的变化,并降低了炎症细胞因子TNF-α和IL-17A的水平。PLE还可以降低IMQ模型诱导的TLR4、MyD88、p-NF-κBp65、p-IκBα、p-PI3K和p-AKT的蛋白表达水平。我们的研究结果表明,PLE在改善银屑病样症状方面是有效的,这可能归因于对TLR4/NF-κB和PI3K/AKT炎症途径的抑制。我们的研究证明了PLE作为一种天然来源治疗银屑病的潜在机制。然而,需要注意的是,这些发现缺乏临床验证,需要进一步的研究在临床环境中验证这些结果。此外,与现有的生物制剂相比,PLE显示出作为一种具有成本效益的替代方案的潜力,这可能对未来银屑病的治疗产生更广泛的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/59619a7c372e/pone.0322710.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/edea6dd21845/pone.0322710.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/6d5ed54ae86e/pone.0322710.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/4e281864d8c4/pone.0322710.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/fc6095ddd76d/pone.0322710.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/d727a13dbb7c/pone.0322710.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/59619a7c372e/pone.0322710.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/edea6dd21845/pone.0322710.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/6d5ed54ae86e/pone.0322710.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/4e281864d8c4/pone.0322710.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/fc6095ddd76d/pone.0322710.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/d727a13dbb7c/pone.0322710.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12057870/59619a7c372e/pone.0322710.g006.jpg

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本文引用的文献

[1]
Birinapant improves imiquimod-induced psoriasis in BALB/c mice.

Immunopharmacol Immunotoxicol. 2025-4

[2]
Amlexanox ameliorates imiquimod-induced psoriasis-like dermatitis by inhibiting Th17 cells and the NF-κB signal pathway.

Biomed Pharmacother. 2025-3

[3]
Neochlorogenic acid ameliorates allergic airway inflammation by suppressing type 2 immunity and upregulating HO-1 expression.

Int Immunopharmacol. 2025-1-27

[4]
Flavonoids attenuate inflammation of HGF and HBMSC while modulating the osteogenic differentiation based on microfluidic chip.

J Transl Med. 2024-11-2

[5]
Integrating network pharmacology, molecular docking, and experimental validation to reveal the mechanism of Radix Rehmanniae in psoriasis.

Medicine (Baltimore). 2024-10-25

[6]
In vitro antioxidant and protective effects of the extract of Broussonetia papyrifera leaves on imiquimod-induced skin lesions in psoriasis-like mice.

Pak J Pharm Sci. 2024-5

[7]
Tetrastigma hemsleyanum polysaccharides alleviate imiquimod-induced psoriasis-like skin lesions in mice by modulating the JAK/STAT3 signaling pathway.

Phytomedicine. 2024-10

[8]
Orientin alleviates the inflammatory response in psoriasis like dermatitis in BALB/c mice by inhibiting the MAPK signaling pathway.

Int Immunopharmacol. 2024-6-15

[9]
ZBP1-mediated apoptosis and inflammation exacerbate steatotic liver ischemia/reperfusion injury.

J Clin Invest. 2024-5-14

[10]
Combined untargeted metabolomics and network pharmacology approaches to reveal the therapeutic role of withanolide B in psoriasis.

J Pharm Biomed Anal. 2024-8-1

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