4.7 Article

Effects of Photobiomodulation on High Glucose Induced Oxidative Stress in Human Embryonic Skin Fibroblasts

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/JSTQE.2021.3054050

Keywords

Photobiomodulation; human embryonic skin fibroblasts; reactive oxygen species; antioxidant enzymes; matrix metalloproteinases

Funding

  1. National Natural Science Foundation ofChina [61705164, 61905177, 61201106]
  2. Tianjin Natural Science Foundation of China [19JCQNJC01600, 19JCQNJC01400]
  3. Tianjin Special Program of Science and Technology [19JCTPJC47900]

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The study demonstrated that PBM has positive effects on functional damage of human embryonic skin fibroblasts by promoting cell proliferation, enhancing antioxidant enzyme activity, stimulating cytokine secretion, inhibiting matrix metalloproteinase expression, and promoting wound healing.
In this study, we explored the effects of photobiomodulation (PBM) on the functional damage of human embryonic skin fibroblasts (CCC-ESFs) in a high glucose environment, as well as the effects of PBM on tissue repair, to provide a theoretical basis for application and promotion of dual-wavelength laser therapy in clinical practices. CCC-ESFs were cultured in vitro for 2 d in a high glucose medium, and then irradiated with a 635/808 nm dual-wavelength semiconductor laser at a dose of 20 mW/cm(2), 0-24 J/cm(2). Cell proliferation, reactive oxygen species (ROS) production, antioxidant enzyme activity (CAT, SOD), lipid oxidization capacity (MDA), cell growth factors, and the expression of matrix metalloproteinases (MMPs) and matrix metalloproteinase inhibitors (TIMPs) were assessed. We found that PBM can enhance the proliferation of fibroblasts, improve the inhibitory effects of the high glucose environment on cell proliferation, increase intracellular ROS production, enhance the activity of antioxidant enzymes, and stimulate cytokine secretion. Furthermore, PBM was found to inhibit the expression of MMPs, increase the expression of TIMPs, reverse the overexpression of MMPs/TIMPs caused by high glucose, and promote wound healing.

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