1,25-Dihydroxyvitamin D3 reduces early mortality post severe burn injury via alleviating endotoxemia, oxidative stress and inflammation

被引:1
|
作者
Chen, Yu [1 ]
Guo, Jing Hui [2 ]
Chen, Ya Jie [1 ]
Huang, Yong [1 ]
Zhang, Cheng [1 ]
Zhang, Qiong [1 ]
Li Gong, Ya [1 ]
Chen, Jing [1 ]
机构
[1] Army Med Univ, Mil Med Univ 3, State Key Lab Trauma & Chem Poisoning China, Inst Burn Res,Southwest Hosp,Affiliated Hosp 1, Gao Tan Yan St, Chongqing 400038, Peoples R China
[2] Chinese Univ Hong Kong, Sch Med, Shenzhen, Guangdong, Peoples R China
关键词
1; 25-Dihydroxyvitamin D3; Severe burn injury; LPS; Oxidative stress; Inflammation; VITAMIN; ADMISSION; OUTCOMES; SEPSIS; LEVEL;
D O I
10.1016/j.burns.2024.05.009
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Severe burn patients frequently suffer from 1,25-Dihydroxyvitamin D3 (1,25-[OH]2-D3) deficiency. In this study, we investigated the effect of 1,25-[OH]2-D3 on early mortality post severe burn and potential underlying mechanisms. Our results indicate that 1,25-[OH]2-D3 significantly reduced early mortality in mice post severe burn injury. A decrease in serum lipopolysaccharide levels and an increase in serum superoxide dismutase activity were found after administration of 1,25-[OH]2-D3. Furthermore, 1,25-[OH]2-D3 demonstrated protective effects on both intestinal and lung histology and ameliorated lung inflammation. Its anti-inflammatory effect was further confirmed in airway epithelial cells. In conclusion, our study provides evidence that 1,25-[OH]2-D3 has a significant impact on the reduction of early mortality post severe burn injury, possibly through its ability to alleviate endotoxemia, oxidative stress, and inflammation. Our findings highlight the potential of 1,25-[OH]2-D3 to protect the intestinal mucosal barrier in the early stage following major burn injury and opens up new avenues for clinical application of 1,25-[OH]2-D3 in burn patients. (c) 2024 Elsevier Ltd and ISBI. All rights reserved.
引用
收藏
页码:1790 / 1798
页数:9
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