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Effect of Lipoxin A4 on Myocardial Ischemia Reperfusion Injury Following Cardiac Arrest in a Rabbit Model
Authors:Zhiqiao Chen  Zhe Wu  Congxin Huang  Yan Zhao  Yirong Zhou  Xianlong Zhou  Xingxing Lu  Lele Mao  Siying Li
Affiliation:1. Renmin Hospital of Wuhan University, 238 JieFang Road, Wuhan, 430060, People’s Republic of China
2. Emergency Center, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, People’s Republic of China
3. Medical College of Wuhan University, 115 Donghu Road, Wuhan, 430071, People’s Republic of China
4. Department of Cardiology, Renmin Hospital of Wuhan University, 238 JieFang Road, Wuhan, 430060, People’s Republic of China
Abstract:In the present study, we investigated the effect of lipoxin A4 on myocardial ischemia–reperfusion injury (IRI) following cardiac arrest (CA) in a rabbit model. Lipoxin A4 is a metabolite of arachidonic acid in the eicosanoid, it is called “brake signal” for its anti-inflammatory activity. Some inflammatory factors (IL-1β, IL-6, TNF-α, and IL-10), NF-κB p65, infarct ratios, apoptotic index, cardiac troponin I (cTnI), hemodynamic and myocardial structures were measured or observed in different groups. Lipoxin A4 inhibits the expression of IL-1β, IL-6, and TNF-α, the values of the infarct ratios, apoptotic index, the level of serum cTnI and NF-κB p65. Meanwhile, it improves the expression of IL-10, hemodynamic, myocardial structure, and function. These indicate that lipoxin A4 mitigates postresuscitation myocardial IRI in which anti-inflammation and suppression of NF-κB activation may play an important role.
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