期刊
ANTIOXIDANTS
卷 10, 期 10, 页码 -出版社
MDPI
DOI: 10.3390/antiox10101609
关键词
skin aging; Kaempferia parviflora; 5,7,4 & PRIME; trimethoxyflavone ; human dermal fibroblasts; tumor necrosis factor-alpha; reactive oxygen species; inflammation
资金
- National Research Foundation of Korea (NRF) [2019R1F1A1059173]
- Bio & Medical Technology Development Program of the National Research Foundation (NRF) - Ministry of Science ICT [2020M3A9E4104380]
- National Research Foundation of Korea [2019R1F1A1059173, 2020M3A9E4104380] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
The study demonstrated the skin protective effects of polymethoxyflavones against oxidative stress and inflammation-induced damage in human dermal fibroblasts. Among the tested compounds, 5,7,4' trimethoxyflavone was identified as the most potent constituent in preventing TNF-alpha-induced HDF damage, inhibiting MMP-1 production, stimulating COLIA1 expression, and suppressing ROS and pro-inflammatory mediators in HDFs. The findings suggest that TMF may be a potential agent for preventing skin aging and dermatological disorders related to oxidative stress and inflammation.
Similar to other organs, the skin undergoes a natural aging process. Moreover, constant direct exposure to environmental stresses, including ultraviolet irradiation, causes the signs of skin aging to appear rather early. Reactive oxygen species (ROS) and inflammatory responses accelerate skin damage in extrinsic aging. In this study, we aimed to investigate the skin protective effects of polymethoxyflavones found in Kaempferia parviflora against oxidative stress and inflammation-induced damage in human dermal fibroblasts (HDFs) stimulated by tumor necrosis factor-alpha (TNF-alpha). The experimental data identified 5,7,4 & PRIME; trimethoxyflavone (TMF) as the most potent constituent in preventing TNF-alpha-induced HDF damage among the tested compounds and it was not only effective in inhibiting matrix metalloproteinase-1 (MMP-1) production but also in stimulating collagen, type I, and alpha 1 (COLIA1) expression. TMF suppressed TNF-alpha-stimulated generation of ROS and pro-inflammatory mediators, such as cyclooxygenase-2 (COX-2), interleukin (IL)-1 beta, and IL-6 in HDFs. TMF also inhibited the pathways regulating fibroblast damage, including mitogen-activated protein kinase (MAPK), activator protein 1 (AP-1), and nuclear factor-kappa B (NF-kappa B). In conclusion, TMF may be a potential agent for preventing skin aging and other dermatological disorders associated with oxidative stress and inflammation.
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