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银屑病配方制剂PSORI-CM01通过核因子κB的表达抑制角质形成细胞中炎性细胞因子和趋化因子的释放。

Formula PSORI-CM01 inhibits the inflammatory cytokine and chemokine release in keratinocytes via NF-κB expression.

作者信息

Han Ling, Sun Jing, Lu Chuan-Jian, Zhao Rui-Zhi, Lu Yue, Lin Han-Jie, Wei Jian-An

机构信息

The Second Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, Guangdong 510006, China.

Dermatology Department, Guangdong Provincial Hospital of Chinese Medicine, Guangdong 510120, China.

出版信息

Int Immunopharmacol. 2017 Mar;44:226-233. doi: 10.1016/j.intimp.2017.01.023. Epub 2017 Jan 25.

Abstract

Psoriasis is a common chronic inflammatory disease in which T-helper 1(Th1) and T-helper 17(Th17) cells play an important role in its pathology. Formula PSORI-CM01 was a novel formulated Chinese medicine used for psoriasis therapy. It had been demonstrated previously that PSORI-CM01 and serum contained Formula PSORI-CM01 (PCM01CS) could improve psoriasis by inhibiting the epithelial hyperplasia, how PSORI-CM01 affects inflammatory cytokine and chemokine in dermis is still unknown. In this study we found PSORI-CM01 pre-treated 3days before IMQ painting could ameliorated IMQ-induced mice skin lesion as PASI score was apparently reduced. Th1 related cytokine IFN-γ and Th17 related cytokine IL-17/IL-22 was used to induce inflammatory models on human keratinocyte cell line HaCaT in vitro, respectively. PCM01CS significantly reduced IFN-γ induced mRNA expression of IL-6, IL-12 and CXCL-10, reduced IL-6 and CXCL-10 release into HaCaT supernatant. 20ng/ml IL-17/IL-22 co-stimulation significantly upregulated expression of IL-6, IL-8 and CCL20 mRNA expression in HaCaT cells, PCM01CS significantly inhibit these cytokines expression both in mRNA and in protein levels. Finally, PCM01CS could obviously inhibit nuclear NF-κB p65 expression which activated by IFN-γ and IL-17/IL-22 stimulation. Thus, our new findings reveal that Formula PSORI-CM01 may possess therapeutic action on psoriasis by inhibiting inflammatory within skin environments.

摘要

银屑病是一种常见的慢性炎症性疾病,其中辅助性T细胞1(Th1)和辅助性T细胞17(Th17)在其病理过程中起重要作用。PSORI-CM01配方是一种用于治疗银屑病的新型中药配方。先前已经证明,PSORI-CM01及含PSORI-CM01的血清(PCM01CS)可通过抑制上皮增生来改善银屑病,但PSORI-CM01如何影响真皮中的炎性细胞因子和趋化因子仍不清楚。在本研究中,我们发现,在涂抹咪喹莫特前3天用PSORI-CM01预处理可改善咪喹莫特诱导的小鼠皮肤病变,因为银屑病面积和严重程度指数(PASI)评分明显降低。分别使用Th1相关细胞因子干扰素-γ(IFN-γ)和Th17相关细胞因子白细胞介素-17(IL-17)/白细胞介素-22(IL-22)在体外人角质形成细胞系HaCaT上诱导炎症模型。PCM01CS显著降低IFN-γ诱导的白细胞介素-6(IL-6)、白细胞介素-12(IL-12)和CXC趋化因子配体10(CXCL-10)的mRNA表达,减少IL-6和CXCL-10释放到HaCaT细胞上清液中。20纳克/毫升IL-17/IL-22共刺激显著上调HaCaT细胞中IL-6、白细胞介素-8(IL-8)和CC趋化因子配体20(CCL20)的mRNA表达,PCM01CS在mRNA和蛋白质水平上均显著抑制这些细胞因子的表达。最后,PCM01CS可明显抑制由IFN-γ和IL-17/IL-22刺激激活的核转录因子κB p65(NF-κB p65)的表达。因此,我们的新发现表明,PSORI-CM01配方可能通过抑制皮肤内环境中的炎症对银屑病具有治疗作用。

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