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The aim of this study was to evaluate the wrinkle improving effect of hyaluronic acid intakes. Wrinkles were induced by exposing the skin of hairless mice to ultraviolet B (UVB) irradiation for 14 weeks. Hyaluronic acid was administered to the mice for 14 weeks including 4 weeks before experiments. Skin tissue was assayed by enzyme-linked immunosorbent assay to determine protein expression of wrinkle-related markers. The group supplemented with high concentrations of hyaluronic acid appeared significantly better than control group for collagen, matrix metalloproteinase 1, interleukin (IL)-1β, and IL-6 assay. Transforming growth factor-β1 (TGF-β1) and hyaluronic acid synthase 2 (HAS-2) were not shown to be significantly different. In conclusion, hyaluronic acid administration regulated expression levels of proteins associated with skin integrity, and improved the wrinkle level in skin subjected to UVB irradiation.

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Osteoarthritis (OA) is a chronic degenerative disease that involves inflammation and pain due to damage or degenerative changes in the cartilage that protects the joints. OA has a high incidence in the elderly. Treatment methods include relieving symptoms and preventing cartilage damage. Drugs used to treat osteoarthritis have side effects and it is important to reduce them. Therefore, it is necessary to develop a therapeutic agent for osteoarthritis using natural substances. The purpose of this experiment was the anti‐inflammation effect of natural substances on osteoarthritis in primary cultured rat cartilage chondrocytes. Aggrecan, collagen type I, □, □, MMP‐3, 7, NK‐kB and COX‐2 expression were measured by real‐time PCR. TNF‐α and IL‐1β secretion was measured by ELISA kit. H2O2 and LPS‐induced chondrocytes were used to measure concentrations of 100, 200, and 400 (μg/ml). As a result, S400 significantly increased the gene expression level of aggrecan, collagen type I, II, III and decreased gene expression of pro‐inflammatory factors NF‐kB, COX‐2 and MMPs (3 and 7). The cytokine productions of TNF‐α and IL‐1β also decreased in S400. Therefore, S400 had an anti‐inflammatory effect and alleviated the inflammation occurs in OA.This abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal.

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