Reynoutria japonica consisted of emodin-8-β-D-glucoside ameliorates Dermatophagoides farinae extract-induced atopic dermatitis-like skin inflammation in mice by inhibiting JAK/STAT signaling

被引:3
|
作者
Shim, Ki-Shuk [1 ]
Song, Hyun Kyung [1 ,2 ]
Park, Musun [3 ]
Kim, Hye Jin [1 ]
Jang, Seol [1 ]
Kim, Taesoo [1 ]
Kim, Ki Mo [1 ,4 ]
机构
[1] Korea Inst Oriental Med, KM Convergence Res Div, Yuseong-Daero 1672, Daejeon 34054, South Korea
[2] Honam Natl Inst Biol Resources, Pract Res Div, Gohadoan-Gil 99, Mokpo 58762, Jeonranamdo, South Korea
[3] Korea Inst Oriental Med, KM Data Div, Yuseong-Daero 1672, Daejeon 34054, South Korea
[4] Univ Sci & Technol UST, Korean Convergence Med Major KIOM, Daejeon 34054, South Korea
关键词
Reynoutria japonica; Dermatophagoides farinae; Atopic dermatitis; Inflammation; JAK/STAT signaling; HOUSE-DUST MITE; BARRIER FUNCTION; CHEMOKINES; FILAGGRIN; JAK1; ACTIVATION; BINDING; REGION; EMODIN; CELLS;
D O I
10.1016/j.biopha.2024.116765
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by skin barrier dysfunction and chronic inflammatory responses. Reynoutria japonica, known as Huzhang in traditional Chinese Medicine, can enhance blood circulation to eliminate wind pathogens and terminate coughing. Despite pharmacological evidence supporting the efficacy of R. japonica in suppressing edema-induced skin inflammation or connective tissue diseases, its pharmaceutical potential for treating AD-like skin inflammation remains unexplored. This study investigated the possible effects of R. japonica ethanol extract (RJE) on Dermatophagoides farinae extract (DfE)induced AD-like skin inflammation in NC/Nga mice. To elucidate the underlying mechanisms by which RJE inhibits skin inflammation, we examined the effect of RJE on IFN-gamma/TNF-alpha-induced signal transducer and activator of transcription (STAT) signaling in human epidermal keratinocytes (HEKs) and human dermal fibroblasts (HDFs). Our findings revealed that RJE mitigates DfE-induced AD-like symptoms and skin barrier disruptions in mouse skin lesions. Moreover, RJE attenuated DfE-induced mast cell infiltration and serum levels of inflammatory cytokines (IL-1 alpha, IL-1 beta, IL-6, IL-23, IFN-gamma, TNF-alpha, and GM-CSF). RJE also inhibited IFN-gamma/TNF-alpha-induced chemokine levels and STAT3 phosphorylation in HEKs and HDFs. Virtual binding analysis of the RJE components suggested that emodin-8-beta-D-glucoside binds to Janus kinase (JAK) 1/2, thereby suppressing STAT signaling, which was confirmed by Western blot analysis. In conclusion, our results suggest that RJE may alleviate DfEinduced skin barrier dysfunction by inhibiting JAK/STAT signaling and the proinflammatory immune response through the suppression of inflammatory mediators in AD-like skin disease. These findings suggest that RJE has potential as an effective therapy for AD management.
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页数:14
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