Inflammatory mechanisms and intervention strategies for sepsis-induced myocardial dysfunction

被引:23
作者
Nong, Yuxin [1 ]
Wei, Xuebiao [2 ]
Yu, Danqing [1 ]
机构
[1] Guangdong Prov Peoples Hosp, Guangdong Acad Med Sci, Guangdong Cardiovasc Inst, Dept Cardiol,Guangdong Prov Key Lab Coronary Heart, Guangzhou, Peoples R China
[2] Guangdong Prov Peoples Hosp, Guangdong Acad Med Sci, Guangdong Prov Geriatr Inst, Dept Geriatr Intens Med, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
host-pathogen interactions; inflammation; myocardial dysfunction; sepsis; targeted therapy; DISSEMINATED INTRAVASCULAR COAGULATION; INDUCED CARDIAC DYSFUNCTION; SPECKLE TRACKING ECHOCARDIOGRAPHY; AUTONOMIC NERVOUS-SYSTEM; INNATE IMMUNE-RESPONSES; SEPTIC SHOCK; MITOCHONDRIAL DYSFUNCTION; CARDIOMYOCYTE CONTRACTILITY; MACROPHAGE POLARIZATION; UNCOUPLING PROTEIN-2;
D O I
10.1002/iid3.860
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sepsis-induced myocardial dysfunction (SIMD) is the leading cause of death in patients with sepsis in the intensive care units. The main manifestations of SIMD are systolic and diastolic dysfunctions of the myocardium. Despite our initial understanding of the SIMD over the past three decades, the incidence and mortality of SIMD remain high. This may be attributed to the large degree of heterogeneity among the initiating factors, disease processes, and host states involved in SIMD. Previously, organ dysfunction caused by sepsis was thought to be an impairment brought about by an excessive inflammatory response. However, many recent studies have shown that SIMD is a consequence of a combination of factors shaped by the inflammatory responses between the pathogen and the host. In this article, we review the mechanisms of the inflammatory responses and potential novel therapeutic strategies in SIMD.
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页数:17
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