Sepsis-related organ dysfunction and shock are primary causes of death in critical illness
which is triggered by pathogen associated molecules patterns (PAMPs) and progresses into life threatening stages as a result of systemic dysfunction in inflammatory reactions
coagulation cascades and immune responses. Advances in our understanding of pathogenesis in sepsis prompt different kinds of anti-sepsis strategies. Unfortunately
there is no specific agent for sepsis except for recombinant human activated protein C
which is withdrawn because of its severe adverse effects. Therefore
it is significant to reevaluate the drugs in clinic and reconsider the strategies in preclinical or clinical studies. Herein
we discuss the therapeutic approaches for sepsis that affect different stages of sepsis progression
their efficacy in treating sepsis
and possible fields for discovering new agents for sepsis treatment.
Mitochondrial preconditioning of pericytes attenuates pulmonary vascular leakage in sepsis-induced rats
Effect and underlying mechanism of L-carnitine improving myocardial systolic dysfunction in sepsis mice
PD-1-mediated CD4+ T cell exhaustion exacerbates gut microbiota translocation in mouse model of sepsis
ATF3 regulates macrophage autophagy and inflammatory responses by suppressing ATG5 and ATG16L1 expression
Protective effect of remimazolam on intestinal barrier function in septic mice
Related Author
DU Zhongyuan
LIU Yiyan
BAO Daiqin
ZHAO Yibo
GUO Juncai
LI Yuxuan
LIU Liangming
LI Tao
Related Institution
The First School of Clinical Medicine, Nanjing Medical University
School of Basic Medical Sciences, Southwest Medical University
School of Pharmacy and Bioengineering, Chongqing University of Technology
National Key Laboratory of Trauma and Chemical Poisoning,Department of War Trauma, Shock and Blood Transfusion,Daping Hospital, Army Medical University