Hydrogen gas inhalation protects against cutaneous ischaemia/reperfusion injury in a mouse model of pressure ulcer |
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Authors: | Wei Fang Guizhen Wang Luyan Tang Huilin Su Huyan Chen Wanqing Liao Jinhua Xu |
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Affiliation: | 1. Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, China;2. The Shanghai Institute of Dermatology, Shanghai, China;3. Department of Dermatology and Venereology, Changzheng Hospital, Shanghai Key Laboratory of Molecular Medical Mycology, Shanghai, China;4. Emergency room, Shanghai Tenth People's Hospital of Tongji University, Shanghai, China |
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Abstract: | Pressure ulcer formation depends on various factors among which repetitive ischaemia/reperfusion(I/R) injury plays a vital role. Molecular hydrogen (H2) was reported to have protective effects on I/R injuries of various internal organs. In this study, we investigated the effects of H2 inhalation on pressure ulcer and the underlying mechanisms. H2 inhalation significantly reduced wound area, 8‐oxo‐dG level (oxidative DNA damage) and cell apoptosis rates in skin lesions. H2 remarkably decreased ROS accumulation and enhanced antioxidant enzymes activities by up‐regulating expression of Nrf2 and its downstream components in wound tissue and/or H2O2‐treated endothelia. Meanwhile, H2 inhibited the overexpression of MCP‐1, E‐selectin, P‐selectin and ICAM‐1 in oxidant‐induced endothelia and reduced inflammatory cells infiltration and proinflammatory cytokines (TNF‐α, IL‐1, IL‐6 and IL‐8) production in the wound. Furthermore, H2 promoted the expression of pro‐healing factors (IL‐22, TGF‐β, VEGF and IGF1) and inhibited the production of MMP9 in wound tissue in parallel with acceleration of cutaneous collagen synthesis. Taken together, these data indicated that H2 inhalation suppressed the formation of pressure ulcer in a mouse model. Molecular hydrogen has potentials as a novel and alternative therapy for severe pressure ulcer. The therapeutic effects of molecular hydrogen might be related to its antioxidant, anti‐inflammatory, pro‐healing actions. |
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Keywords: | hydrogen inflammation oxidative stress pressure ulcer reperfusion injury wound healing |
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