1,25-Dihydroxyvitamin D3 reduces early mortality post severe burn injury via alleviating endotoxemia, oxidative stress and inflammation.
Yu ChenJing Hui GuoYa Jie ChenYong HuangCheng ZhangQiong ZhangYa Li GongJing ChenPublished in: Burns : journal of the International Society for Burn Injuries (2024)
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.
Keyphrases
- oxidative stress
- wound healing
- end stage renal disease
- early stage
- early onset
- cardiovascular events
- ejection fraction
- newly diagnosed
- peritoneal dialysis
- dna damage
- inflammatory response
- lps induced
- prognostic factors
- risk factors
- drug induced
- cardiovascular disease
- induced apoptosis
- metabolic syndrome
- type diabetes
- toll like receptor
- diabetic rats
- hydrogen peroxide
- insulin resistance
- skeletal muscle
- high resolution
- immune response
- climate change
- human health
- replacement therapy
- rectal cancer