郑州大学学报(医学版)
鄭州大學學報(醫學版)
정주대학학보(의학판)
JOURNAL OF ZHENGZHOU UNIVERSITY(MEDICAL SCIENCES)
2013年
5期
640-642,643
,共4页
孙涛%万大国%宋恒良%孙慎杰
孫濤%萬大國%宋恆良%孫慎傑
손도%만대국%송항량%손신걸
瑞舒伐他汀%miR-126%血管再生%急性心肌梗死%大鼠
瑞舒伐他汀%miR-126%血管再生%急性心肌梗死%大鼠
서서벌타정%miR-126%혈관재생%급성심기경사%대서
rosuvastatin%miR-126%angiogenesis%acute myocardial infarction%rat
目的:探讨瑞舒伐他汀能否上调大鼠急性心肌梗死后梗死组织miR-126的表达以及其与血管再生的关系。方法:54只大鼠建立急性心肌梗死模型后随机分为模型组27只和瑞舒伐他汀组27只。次日起瑞舒伐他汀组给予瑞舒伐他汀10 mg/( kg· d)连续灌胃6周,模型组给予等量助溶溶剂连续灌胃6周。处死动物,取梗死组织,采用免疫组化SP法检测心肌组织微血管密度(MVD),采用实时荧光定量PCR法检测miR-126的表达水平。结果:与模型组相比,瑞舒伐他汀组梗死组织MVD增大,miR-126的表达水平升高(t=2.386和3.264,P<0.05);瑞舒伐他汀组梗死组织MVD和miR-126的表达水平呈正相关(r=0.720,P=0.026)。结论:瑞舒伐他汀可能通过上调miR-126的表达促进心肌梗死大鼠梗死心肌组织的血管再生。
目的:探討瑞舒伐他汀能否上調大鼠急性心肌梗死後梗死組織miR-126的錶達以及其與血管再生的關繫。方法:54隻大鼠建立急性心肌梗死模型後隨機分為模型組27隻和瑞舒伐他汀組27隻。次日起瑞舒伐他汀組給予瑞舒伐他汀10 mg/( kg· d)連續灌胃6週,模型組給予等量助溶溶劑連續灌胃6週。處死動物,取梗死組織,採用免疫組化SP法檢測心肌組織微血管密度(MVD),採用實時熒光定量PCR法檢測miR-126的錶達水平。結果:與模型組相比,瑞舒伐他汀組梗死組織MVD增大,miR-126的錶達水平升高(t=2.386和3.264,P<0.05);瑞舒伐他汀組梗死組織MVD和miR-126的錶達水平呈正相關(r=0.720,P=0.026)。結論:瑞舒伐他汀可能通過上調miR-126的錶達促進心肌梗死大鼠梗死心肌組織的血管再生。
목적:탐토서서벌타정능부상조대서급성심기경사후경사조직miR-126적표체이급기여혈관재생적관계。방법:54지대서건립급성심기경사모형후수궤분위모형조27지화서서벌타정조27지。차일기서서벌타정조급여서서벌타정10 mg/( kg· d)련속관위6주,모형조급여등량조용용제련속관위6주。처사동물,취경사조직,채용면역조화SP법검측심기조직미혈관밀도(MVD),채용실시형광정량PCR법검측miR-126적표체수평。결과:여모형조상비,서서벌타정조경사조직MVD증대,miR-126적표체수평승고(t=2.386화3.264,P<0.05);서서벌타정조경사조직MVD화miR-126적표체수평정정상관(r=0.720,P=0.026)。결론:서서벌타정가능통과상조miR-126적표체촉진심기경사대서경사심기조직적혈관재생。
Aim:To investigate whether rosuvastatin could up-regulate the expression of miR-126 after acute myocardi-al infarction in rats and study its relationship with angiogenesis .Methods:A total of 54 rats were established acute myocar-dial infarction model and randomly allocated into the model group and the rosuvastatin group with 27 in each group .Then the rats in the rosuvastatin group were given rosuvastatin at 10 mg/(kg· d) by gavage for 6 weeks, and those in the model group were given equivalent solvent .After 6 weeks,the rats were executed and the myocardial infarction samples were pre-pared .The myocardial microvessel density was detected by immunohistochemical staining , and the expression level of miR-126 was determined by real time PCR .Results:Compared with the model group , the microvessel density and the expres-sion level of miR-126 in rosuvastatin group obviously elevated (t=2.386 and 3.264,P <0.05); the 2 parameters were positively related in myocardial infarction tissue of rosuvastatin group (r=0.720, P=0.026).Conclusion: Rosuvastatin may promote angiogenesis in rat infarction myocardium by upregulating the expression of miR -126.