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养血解毒汤通过外泌体 HSP70 分泌调控 TLR4/NF-κB 信号通路对银屑病样损伤的保护作用。

Protective effect of Yangxue Jiedu Soup against psoriasis-like lesions by regulating TLR4/NF-κB signaling pathway mediated by secretion of exosome HSP70.

机构信息

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing 100010, China.

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing 100010, China; Beijing Institute of Chinese Medicine, Beijing 100010, China.

出版信息

Biomed Pharmacother. 2022 Mar;147:112604. doi: 10.1016/j.biopha.2021.112604. Epub 2022 Jan 5.

Abstract

Psoriasis is a common chronic inflammatory hypertrophic skin disease characterized by abnormal proliferation and differentiation of keratinocyte and immune T cell. The pathogenesis of psoriasis has not been fully elucidated and there is no effective therapy in clinic. As a traditional Chinese medicine formula, Yangxue Jiedu Soup (YJS) has been used to treat inflammatory diseases caused by Yin Deficiency and Blood Dryness. The purpose of present study was to investigate the therapeutic effect and molecular mechanism of YJS on psoriasis model mice. Results showed that YJS effectively inhibited the hypertrophy, erythema and scales of psoriasis-like lesions to alleviate the pathological changes of skin lesions, and further decreased the production of TNF-α, IL-6, IL-1β, IFN-γ, IL-17 and IL-23. Meanwhile, YJS also significantly reduced keratinocyte proliferation and maintained immune system balance by inhibiting the expression of PCNA, Ki-67, CD4 + and CD8 + in psoriasis mice. Moreover, the results further indicated that YJS could inhibit TLR4 activation and NF-κB p65 nuclear transfer by suppressing HSP70 secretion to attenuate the inflammatory response in IMQ-induced mice, which provided a theoretical basis for the clinical use of YJS in the treatment of psoriasis.

摘要

银屑病是一种常见的慢性炎症性增生性皮肤病,其特征是角质形成细胞和免疫 T 细胞的异常增殖和分化。银屑病的发病机制尚未完全阐明,临床上尚无有效的治疗方法。养血解毒汤(YJS)作为一种中药方剂,已被用于治疗阴虚血燥引起的炎症性疾病。本研究旨在探讨 YJS 对银屑病模型小鼠的治疗作用及分子机制。结果表明,YJS 能有效抑制银屑病样皮损的肥大、红斑和鳞屑,减轻皮肤病变的病理变化,进一步降低 TNF-α、IL-6、IL-1β、IFN-γ、IL-17 和 IL-23 的产生。同时,YJS 通过抑制 PCNA、Ki-67、CD4+和 CD8+在银屑病小鼠中的表达,也显著抑制角质形成细胞增殖,维持免疫系统平衡。此外,研究结果还表明,YJS 可以通过抑制 HSP70 的分泌来抑制 TLR4 的激活和 NF-κB p65 的核转位,从而减轻 IMQ 诱导的小鼠的炎症反应,为 YJS 临床用于治疗银屑病提供了理论依据。

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