Gut-Lung Crosstalk in Sepsis-Induced Acute Lung Injury

被引:48
|
作者
Zhou, Xin [1 ]
Liao, Youxia [1 ]
机构
[1] Wuhan Univ, Wuhan Hosp 3, Dept ICU Emergency, Wuhan, Peoples R China
关键词
sepsis; acute lung injury; gut-lung crosstalk; inflammation; gut microbiome; RESPIRATORY-DISTRESS-SYNDROME; CRITICALLY-ILL PATIENTS; TRIMETHYLAMINE-N-OXIDE; IMPROVES SURVIVAL; VITAMIN-C; MICROBIOTA; PNEUMONIA; SHOCK; THIAMINE; MICE;
D O I
10.3389/fmicb.2021.779620
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are common acute and severe cases of the respiratory system with complicated pathogenesis and high mortality. Sepsis is the leading indirect cause of ALI/ARDS in the intensive care unit (ICU). The pathogenesis of septic ALI/ARDS is complex and multifactorial. In the development of sepsis, the disruption of the intestinal barrier function, the alteration of gut microbiota, and the translocation of the intestinal microbiome can lead to systemic and local inflammatory responses, which further alter the immune homeostasis in the systemic environment. Disruption of homeostasis may promote and propagate septic ALI/ARDS. In turn, when ALI occurs, elevated levels of inflammatory cytokines and the shift of the lung microbiome may lead to the dysregulation of the intestinal microbiome and the disruption of the intestinal mucosal barrier. Thus, the interaction between the lung and the gut can initiate and potentiate sepsis-induced ALI/ARDS. The gut-lung crosstalk may be a promising potential target for intervention. This article reviews the underlying mechanism of gut-lung crosstalk in septic ALI/ARDS.
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收藏
页数:11
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