Anti-Inflammatory and Anti-Apoptotic Effects of Acer Palmatum Thumb. Extract, KIOM-2015EW, in a Hyperosmolar-Stress-Induced In Vitro Dry Eye Model

被引:30
作者
Kim, Yeoun-Hee [1 ,2 ]
Oh, Tae Woo [1 ]
Park, Eunhee [1 ]
Yim, Nam-Hui [1 ]
Park, Kang Il [1 ]
Cho, Won Kyung [1 ]
Ma, Jin Yeul [1 ]
机构
[1] KIOM, Korean Med KM Applicat Ctr, 70 Cheomdan Ro, Daegu 41062, South Korea
[2] Kyungpook Natl Univ, Med Sch, Inst Biomed Engn Res, 90 Chilgokjungang Daero 136 Gil, Bukgu 41405, Daegu, South Korea
关键词
dry eye; human corneal epithelial cells; hyperosmolar stress; anti-inflammation; anti-apoptosis; natural substance; orientin; isoorientin; vitexin; CORNEAL EPITHELIAL-CELLS; NF-KAPPA-B; OCULAR SURFACE; MATRIX METALLOPROTEINASES; SQUAMOUS METAPLASIA; SIGNAL-TRANSDUCTION; SJOGRENS-SYNDROME; MAP KINASES; JNK; INFLAMMATION;
D O I
10.3390/nu10030282
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The aim of this study was to assess the anti-inflammatory and anti-apoptotic effects of KIOM-2015EW, the hot-water extract of maple leaves in hyperosmolar stress (HOS)-induced human corneal epithelial cells (HCECs). HCECs were exposed to hyperosmolar medium and exposed to KIOM-2015EW with or without the hyperosmolar media. Tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, and IL-6 production and apoptosis were observed, and the activation of mitogen-activated protein kinases (MAPKs) including extracellular signal regulated kinase (ERK), p38 and c-JUN N-terminal kinase (JNK) signaling and nuclear factor (NF)-kappa B was confirmed. Compared to isomolar medium, the induction of cell cytotoxicity significantly increased in HCECs exposed to hyperosmolar medium in a time-dependent manner. KIOM-2015EW-treatment significantly reduced the mRNA and protein expression of pro-inflammatory mediators and apoptosis. KIOM-2015EW-treatment inhibited HOS-induced MAPK signaling activation. Additionally, the HOS-induced increase in NF-kappa B phosphorylation was attenuated by KIOM-2015EW. The results demonstrated that KIOM-2015EW protects the ocular surface by suppressing inflammation in dry eye disease, and suggest that KIOM-2015EW may be used to treat several ocular surface diseases where inflammation plays a key role.
引用
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页数:18
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