Enzymatic hydrolysates obtained from Trametes versicolor polysaccharopeptides protect human skin keratinocyte against AAPH‑induced oxidative stress and inflammatory

哈卡特 血红素加氧酶 氧化应激 激酶 p38丝裂原活化蛋白激酶 云芝 MAPK/ERK通路 抗氧化剂 活力测定 化学 蛋白激酶A 下调和上调 角质形成细胞 分子生物学 生物化学 生物 细胞 血红素 体外 漆酶 基因
作者
Chun‐Hsu Chou,Ming‐Shiun Tsai,Hsin‐Yu Lu,Chao‐Kai Chang,Kuan‐Chen Cheng,Mei‐Hsin Jhan,Chang‐Wei Hsieh
出处
期刊:Journal of Cosmetic Dermatology [Wiley]
卷期号:18 (6): 2011-2018 被引量:8
标识
DOI:10.1111/jocd.12959
摘要

Abstract Background Polysaccharopeptides (PSPs) extracted from Trametes versicolor show antitumor, anti‐inflammatory, and immunomodulation effects. According to our previous report, the enzymatic hydrolysates obtained from T versicolor PSPs by 80 U/mL β‐1,3‐D‐glucanase (PSPs‐EH80) did not change the functional groups of PSPs but enhanced their antioxidative activities. However, the mechanism elevating the antioxidant and anti‐inflammatory effect of PSPs‐EH80 is not clear. Aims This research focused on the protective mechanism(s) of PSPs‐EH80 against free radical and 2,2'‐azobis (2‐amidinopropane) dihydrochloride (AAPH)‐induced oxidative damage in human keratinocyte (HaCaT) cells. Methods We evaluated the anti‐inflammatory potential of PSPs‐EH80 by assessing its free radical‐induced oxidative damage. Using the HaCaT cell as the experimental system, we tested the protective effects of PSPs‐EH80 on a model of AAPH‐induced cellular oxidative damage through the assessment of cell survival rate. Heme oxygenase 1 (HO‐1), nuclear factor erythroid 2‐related factor 2 (Nrf2), cyclooxygenase‐2 (COX‐2), nuclear factor kappa‐light‐chain‐enhancer of activated B cells (NF‐κB), extracellular signal‐regulated kinase (ERK), c‐Jun N‐terminal kinase (JNK) and p38 mitogen‐activated protein kinase were determined using MTT assays and Western blotting. Results We demonstrated that PSPs‐EH80 significantly enhanced keratinocyte viability, and augmented the antioxidant HO‐1 expressions through upregulation of the Nrf2, compared with PSPs. Furthermore, PSPs‐EH80 significantly reduced AAPH‐induced COX‐2 expressions through downregulation of the ERK, p38, and NF‐κB signaling pathways. Conclusion The PSPs‐EH80 exhibits a stronger antioxidant and anti‐inflammatory capacity than PSPs. Therefore, PSPs‐EH80 could be effective for attenuating free radical‐induced oxidative damage in human skin and can be applied widely in the fields of cosmetics and medicine.
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