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BRD3308 suppresses macrophage oxidative stress and pyroptosis via upregulating acetylation of H3K27 in sepsis-induced acute lung injury.

Bohao LiuNing LiYi LiuYan ZhangLimei QuHongfei CaiYang LiXiaojing WuQing Geng
Published in: Burns & trauma (2024)
BRD3308 inhibits oxidative stress and pyroptosis in macrophages by modulating histone acetylation, thereby preventing sepsis-induced ALI. The present study provides a potential strategy and theoretical basis for the clinical treatment of sepsis-induced ALI.
Keyphrases
  • diabetic rats
  • oxidative stress
  • high glucose
  • acute kidney injury
  • intensive care unit
  • dna damage
  • drug induced
  • signaling pathway
  • adipose tissue
  • dna methylation
  • ischemia reperfusion injury
  • lipopolysaccharide induced