Shin Kyong-Oh, Kim Sungeun, Kim Bokyung, Park Hye-Yoon, Jung Eunhee, Kim Garyun, Kim Donghee, Cho Hwang Eui, Uchida Yoshikazu, Park Kyungho
Department of Food Science & Nutrition, and Convergence Program of Material Science for Medicine and Pharmaceutics, Hallym University, Chuncheon 24252, Korea.
The Korean Institute of Nutrition, Hallym University, Chuncheon 24252, Korea.
Pharmaceuticals (Basel). 2022 Mar 31;15(4):431. doi: 10.3390/ph15040431.
Air pollutants contribute to the development of diseases such as asthma, chronic obstructive pulmonary disease (COPD), pulmonary cancer, cardiovascular problems, and some skin diseases. We recently found that a major air pollutant, diesel particulate matter (DPM), induces apoptosis in human keratinocytes by increasing a proapoptotic lipid mediator, ceramide. DPM activates nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX), which stimulates sphingomyelinase, leading to an increased conversion of sphingomyelin to ceramide. Interestingly, we characterized that although NOX is a reactive oxygen species (ROS) generator, the activation of sphingomyelinases by NOX is an ROS-independent mechanism. A Korean weed, prostrate spurge Rafin (ESR), has been used for centuries as a folk medicine to treat bronchitis, hepatitis, hemorrhage, and skin inflammation. Flavonoids, terpenes and tannins are enriched in ESR, and although ESR has proven antioxidative activity, its biological activities are largely unknown. Here, we investigate whether and how ESR protects keratinocytes against DPM-mediated apoptosis. We found that ESR-extracts (ESR-Ex) protect keratinocytes from DPM-induced apoptosis by inhibiting NOX activation in keratinocytes in response to DPM. We also demonstrated that ESR-Ex suppresses NOX activation via a blockage of the aryl hydrocarbon receptor (AhR) activation-mediated transcription of neutrophil cytosolic factor 1 (NCF1)/p47phox, a subunit of NOX. Our study reveals previously uncharacterized biological activity of ESR-Ex; i.e., its inhibition of Ahr and NOX activation. Thus, because the inhibition of NOX has already been developed to treat NOX-mediated diseases, including various types of cardiovascular diseases and cancers, initiated by air pollutants and because AhR activation contributes to the development of chronic inflammatory diseases, our study provides further advantages for the medical use of ESR.
空气污染物会促使诸如哮喘、慢性阻塞性肺疾病(COPD)、肺癌、心血管问题以及一些皮肤病等疾病的发生。我们最近发现,一种主要的空气污染物,柴油颗粒物(DPM),通过增加一种促凋亡脂质介质神经酰胺,诱导人角质形成细胞凋亡。DPM激活烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶(NOX),该酶刺激鞘磷脂酶,导致鞘磷脂向神经酰胺的转化增加。有趣的是,我们发现尽管NOX是一种活性氧(ROS)生成器,但NOX对鞘磷脂酶的激活是一种不依赖ROS的机制。一种韩国杂草,平卧大戟Rafin(ESR),几个世纪以来一直被用作民间药物来治疗支气管炎、肝炎、出血和皮肤炎症。ESR富含黄酮类化合物、萜类化合物和单宁,尽管ESR已被证明具有抗氧化活性,但其生物活性在很大程度上仍不为人知。在这里,我们研究ESR是否以及如何保护角质形成细胞免受DPM介导的凋亡。我们发现ESR提取物(ESR-Ex)通过抑制角质形成细胞中对DPM产生反应的NOX激活,保护角质形成细胞免受DPM诱导的凋亡。我们还证明,ESR-Ex通过阻断芳烃受体(AhR)激活介导的中性粒细胞胞质因子1(NCF1)/p47phox(NOX的一个亚基)的转录来抑制NOX激活。我们的研究揭示了ESR-Ex以前未被描述的生物活性;即其对AhR和NOX激活的抑制作用。因此,由于抑制NOX已被开发用于治疗由空气污染物引发的NOX介导的疾病,包括各种类型的心血管疾病和癌症,并且由于AhR激活会导致慢性炎症性疾病的发展,我们的研究为ESR的医学应用提供了进一步的优势。