Effects of antioxidants on skin hydration, inflammatory cytokines, and keratinocyte differentiation markers in a PM10-exposed skin barrier-disrupted mouse model.

IF 3.5 3区 医学
Jin Ho Kim, Mi Hee Kwack, Weon Ju Lee
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引用次数: 0

Abstract

Given that particulate matter (PM) has an established role in inducing oxidative stress, inflammation, and skin aging, it is plausible that PM could exacerbate inflammatory skin conditions such as xerosis. Xerosis represents a significant dermatological concern among older adults within aging populations. We conducted an investigation into the efficacy of antioxidants, such as dieckol, punicalagin, epigallocatechin gallate (EGCG), and resveratrol, against PM10 in a skin barrier-disrupted mouse model. A skin barrier-disrupted mouse model was induced by tape stripping. This study investigated the antioxidative and anti-inflammatory properties of antioxidants on PM-induced changes using the skin barrier-disrupted mouse model. Tape strips were attached to the back of 7-week-old nude mice and removed quickly. To investigate variations in skin hydration, levels of inflammatory cytokines, and indicators of keratinocyte differentiation, mice underwent treatment with several compounds: a control vehicle (100 μL), PM10 100 μL (100 μg/mL), PM10 100 μL (100 μg/mL) with antioxidants 100 μL (Punicalagin 5 μM, Dieckol 5 μM, EGCG 1 μM, resveratol 1 μM) for 1 week. To assess their effects, different analysis were conducted using measurements of skin moisture, real-time polymerase chain reaction, enzyme-linked immunosorbent assay for detecting inflammatory cytokines, and immunofluorescence staining to identify markers of keratinocyte differentiation. While PM10 decreased water content in disrupted skin, all antioxidants preserved skin hydration in the skin barrier-disrupted mice, regardless of the presence of PM10. All antioxidants also inhibited the upregulation of inflammatory cytokines, such as interleukin (IL)-1β, IL-4, IL-6, IL-8, and tumor necrosis factor-alpha and normalized the downregulation of keratinocyte differentiation markers against PM10 in skin barrier-disrupted mice. This study elucidated the protective effects of antioxidants-namely, punicalagin, dieckol, EGCG, and resveratrol-in mitigating the impact of PM10 on skin barrier integrity and inflammation in a disrupted skin barrier mouse model, highlighting their potential utility in dermatological treatments.

在pm10暴露的皮肤屏障破坏小鼠模型中,抗氧化剂对皮肤水合作用、炎症细胞因子和角质细胞分化标志物的影响
鉴于颗粒物(PM)在诱导氧化应激、炎症和皮肤衰老方面具有明确的作用,因此PM可能会加剧炎症性皮肤状况,如干燥症。干燥症是老年人中一个重要的皮肤病问题。我们在皮肤屏障破坏的小鼠模型中研究了抗氧化剂(如二酚、槟榔苷、表没食子儿茶素没食子酸酯(EGCG)和白藜芦醇)对PM10的功效。采用胶带剥离法建立皮肤屏障破坏小鼠模型。本研究利用皮肤屏障破坏小鼠模型研究了抗氧化剂对pm诱导的变化的抗氧化和抗炎特性。将胶带贴在7周大的裸鼠背部,并迅速取下。为了研究皮肤水合作用、炎症细胞因子水平和角质细胞分化指标的变化,小鼠接受了几种化合物的治疗:对照物(100 μL)、PM10 100 μL (100 μg/mL)、PM10 100 μL (100 μg/mL)和抗氧化剂100 μL (Punicalagin 5 μM、Dieckol 5 μM、EGCG 1 μM、白藜芦醇1 μM),持续1周。为了评估其效果,使用皮肤湿度测量、实时聚合酶链反应、检测炎症细胞因子的酶联免疫吸附试验和识别角质细胞分化标记的免疫荧光染色进行了不同的分析。虽然PM10降低了受损皮肤的含水量,但无论PM10是否存在,所有抗氧化剂都能保持皮肤屏障受损小鼠的皮肤水合作用。所有抗氧化剂也抑制炎症细胞因子的上调,如白细胞介素(IL)-1β、IL-4、IL-6、IL-8和肿瘤坏死因子α,并使皮肤屏障破坏小鼠角质细胞分化标志物对PM10的下调正常化。本研究阐明了抗氧化剂的保护作用,即punicalagin, dieckol, EGCG和白藜芦醇,在减轻PM10对皮肤屏障完整性和炎症的影响中,在皮肤屏障受损的小鼠模型中,强调了它们在皮肤病治疗中的潜在效用。
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来源期刊
International Journal of Immunopathology and Pharmacology
International Journal of Immunopathology and Pharmacology Immunology and Microbiology-Immunology
自引率
0.00%
发文量
88
期刊介绍: International Journal of Immunopathology and Pharmacology is an Open Access peer-reviewed journal publishing original papers describing research in the fields of immunology, pathology and pharmacology. The intention is that the journal should reflect both the experimental and clinical aspects of immunology as well as advances in the understanding of the pathology and pharmacology of the immune system.
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