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辛荷他克立散作为银屑病的一种潜在治疗药物:网络药理学与实验验证

Sinhyotaklisan as a Potential Therapeutic for Psoriasis: Network Pharmacology and Experimental Validation.

作者信息

Ahn Jung-Yun, Lim Dong-Woo, Kim Jin-Hee, Park Sung-Yun, Park Sun-Dong, Lee Ju-Hee

机构信息

College of Korean Medicine, Dongguk University, Goyang 10326, Republic of Korea.

Department of Biomedical Laboratory Science, College of Health Science, Cheongju University, Cheongju 28503, Republic of Korea.

出版信息

Int J Mol Sci. 2025 May 25;26(11):5082. doi: 10.3390/ijms26115082.

DOI:10.3390/ijms26115082
PMID:40507893
Abstract

Sinhyotaklisan (SHTLS) is a traditional herbal prescription composed of , , , and , commonly used to treat skin disorders. This study aimed to investigate the therapeutic effects and underlying mechanisms of SHTLS in psoriasis through the network pharmacology analysis and experimental validation in vitro and in vivo. Bioactive compounds and molecular targets were identified using the Traditional Chinese Medicine Systems Pharmacology database, and key protein-protein interaction networks were analyzed via STRING and Cytoscape. In vitro, HaCaT cells were pretreated with SHTLS and stimulated with TNF-α, followed by assessments using proliferation assays, scratch assays, quantitative real-time PCR, and Western blotting. In vivo, the anti-psoriatic effects of SHTLS were evaluated in an imiquimod-induced psoriatic mouse model. A total of 36 key targets were significantly enriched in TNF-α, MAPK, HIF-1α, and IL-17 signaling pathways. SHTLS suppressed TNF-α-induced expression of VEGF and HIF-1α, while upregulating p53, thereby inhibiting keratinocyte hyperproliferation and angiogenesis. It also reduced IL-6 and IL-8 levels and blocked activation of the NF-κB and MAPK pathways. Histological analysis confirmed that SHTLS alleviated psoriatic lesions in vivo. These findings suggest that SHTLS may be a promising therapeutic candidate for psoriasis by targeting hyperproliferation, angiogenesis, and inflammation.

摘要

四和汤(SHTLS)是一种由[具体成分未给出]组成的传统草药方剂,常用于治疗皮肤疾病。本研究旨在通过网络药理学分析以及体外和体内实验验证,探讨四和汤对银屑病的治疗作用及潜在机制。利用中药系统药理学数据库鉴定生物活性化合物和分子靶点,并通过STRING和Cytoscape分析关键的蛋白质-蛋白质相互作用网络。体外实验中,用四和汤预处理HaCaT细胞,并用TNF-α刺激,随后通过增殖实验、划痕实验、定量实时PCR和蛋白质印迹法进行评估。体内实验中,在咪喹莫特诱导的银屑病小鼠模型中评估四和汤的抗银屑病作用。共有36个关键靶点在TNF-α、MAPK、HIF-1α和IL-17信号通路中显著富集。四和汤抑制TNF-α诱导的VEGF和HIF-1α表达,同时上调p53,从而抑制角质形成细胞过度增殖和血管生成。它还降低IL-6和IL-8水平,并阻断NF-κB和MAPK通路的激活。组织学分析证实四和汤在体内减轻了银屑病病变。这些发现表明,四和汤可能通过靶向过度增殖、血管生成和炎症,成为治疗银屑病的有前景的候选药物。

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本文引用的文献

1
Sinhyotaklisan alleviates inflammation in LPS-activated macrophages by modulating the heme oxygenase pathway.辛约塔克利桑通过调节血红素加氧酶途径减轻脂多糖激活的巨噬细胞中的炎症。
J Ethnopharmacol. 2025 Mar 26;344:119548. doi: 10.1016/j.jep.2025.119548. Epub 2025 Feb 25.
2
Based on UPLC-Q-TOF/MS and Network Pharmacology to Explore the Mechanism of Qingre Lishi Decoction in the Treatment of Psoriasis.基于 UPLC-Q-TOF/MS 和网络药理学探讨清热利湿方治疗银屑病的作用机制。
Drug Des Devel Ther. 2024 Aug 28;18:3871-3889. doi: 10.2147/DDDT.S467066. eCollection 2024.
3
Signaling pathways and targeted therapies for psoriasis.
银屑病的信号通路和靶向治疗。
Signal Transduct Target Ther. 2023 Nov 27;8(1):437. doi: 10.1038/s41392-023-01655-6.
4
Multi-target mechanism of for treatment of psoriasis based on network pharmacology and molecular docking.基于网络药理学和分子对接的银屑病治疗多靶点机制
Saudi Pharm J. 2023 Nov;31(11):101788. doi: 10.1016/j.jsps.2023.101788. Epub 2023 Sep 16.
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Current developments and perspectives in psoriasis.银屑病的现状与展望。
J Dtsch Dermatol Ges. 2023 Apr;21(4):363-372. doi: 10.1111/ddg.15033. Epub 2023 Apr 5.
6
Effects of splenectomy on skin inflammation and psoriasis-like phenotype of imiquimod-treated mice.脾切除术对咪喹莫特处理的小鼠皮肤炎症和银屑病样表型的影响。
Sci Rep. 2022 Aug 30;12(1):14738. doi: 10.1038/s41598-022-18900-7.
7
Treatments in psoriasis: from standard pharmacotherapy to nanotechnology therapy.银屑病的治疗:从标准药物疗法到纳米技术疗法。
Postepy Dermatol Alergol. 2022 Jun;39(3):460-471. doi: 10.5114/ada.2021.108445. Epub 2021 Aug 16.
8
The impact of gender and sex in psoriasis: What to be aware of when treating women with psoriasis.性别和性在银屑病中的影响:治疗银屑病女性患者时需注意的事项。
Int J Womens Dermatol. 2022 Apr 13;8(2):e010. doi: 10.1097/JW9.0000000000000010. eCollection 2022 Jun.
9
Advances in the pathogenesis of psoriasis: from keratinocyte perspective.银屑病发病机制的研究进展:从角质形成细胞角度看。
Cell Death Dis. 2022 Jan 24;13(1):81. doi: 10.1038/s41419-022-04523-3.
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The Global, Regional, and National Burden of Psoriasis: Results and Insights From the Global Burden of Disease 2019 Study.银屑病的全球、区域和国家负担:2019年全球疾病负担研究的结果与见解。
Front Med (Lausanne). 2021 Dec 16;8:743180. doi: 10.3389/fmed.2021.743180. eCollection 2021.