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Simvastatin Prevents Lipopolysaccharide-induced Septic Shock in Rats 被引量:1

Simvastatin Prevents Lipopolysaccharide-induced Septic Shock in Rats
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摘要 Simvastatin is a hypolipidemic drug that inhibits hydroxymethylglutaryl coenzyme A(HMGCoA) reductase to control elevated cholesterol,or hypercholesterolemia.Previous studies have shown that simvastatin may attenuate inflammation in ischemia-reperfusion injury and sepsis.Herein,we hypothesized that simvastatin may prevent rats from lipopolysaccharide(LPS)-induced septic shock.In our study,rats were divided into a saline group,an LPS group and an LPS plus simvastatin group.Male Sprague-Dawley(SD) rats were pretreated with simvastatin(1 mg/kg) for 30 min before the addition of LPS(8 mg/kg),with variations in left ventricular pressure recorded throughout.Ninety min after LPS injection,whole blood was collected from the inferior vena cava,and neutrophils were separated from the whole blood using separating medium.The neutrophils were then lysed for Western blotting to detect the levels of urokinase-type plasminogen activator(u PA) and plasminogen activator inhibitor-1(PAI-1).In addition,mesentery microcirculations of inlet diameter,outlet diameter and blood flow rate were measured in all three groups.The results indicated that simvastatin significantly promoted heart systolic function and increased the level of u PA while simultaneously inhibited the expression of PAI-1 as compared with LPS group.Moreover,simvastatin reversed the LPS-induced inhibition of mesentery microcirculation.Taken together,it was suggested that simvastatin can effectively protect the rats from LPS-induced septic shock. Simvastatin is a hypolipidemic drug that inhibits hydroxymethylglutaryl coenzyme A(HMGCoA) reductase to control elevated cholesterol,or hypercholesterolemia.Previous studies have shown that simvastatin may attenuate inflammation in ischemia-reperfusion injury and sepsis.Herein,we hypothesized that simvastatin may prevent rats from lipopolysaccharide(LPS)-induced septic shock.In our study,rats were divided into a saline group,an LPS group and an LPS plus simvastatin group.Male Sprague-Dawley(SD) rats were pretreated with simvastatin(1 mg/kg) for 30 min before the addition of LPS(8 mg/kg),with variations in left ventricular pressure recorded throughout.Ninety min after LPS injection,whole blood was collected from the inferior vena cava,and neutrophils were separated from the whole blood using separating medium.The neutrophils were then lysed for Western blotting to detect the levels of urokinase-type plasminogen activator(u PA) and plasminogen activator inhibitor-1(PAI-1).In addition,mesentery microcirculations of inlet diameter,outlet diameter and blood flow rate were measured in all three groups.The results indicated that simvastatin significantly promoted heart systolic function and increased the level of u PA while simultaneously inhibited the expression of PAI-1 as compared with LPS group.Moreover,simvastatin reversed the LPS-induced inhibition of mesentery microcirculation.Taken together,it was suggested that simvastatin can effectively protect the rats from LPS-induced septic shock.
出处 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2017年第2期226-230,共5页 华中科技大学学报(医学英德文版)
基金 supported by the Wuhan Science and Technology Project,China(No.2013060602010252)
关键词 septic shock lipopolysaccharide urokinase-type plasminogen activator plasminogen activator inhibitor-1 simvastatin septic shock lipopolysaccharide urokinase-type plasminogen activator plasminogen activator inhibitor-1 simvastatin
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