DocumentCode :
3425574
Title :
Effect of atorvastatin combined with coenzyme Q10 on uncoupling protein 2 gene expression in rats with heart failure after myocardial infarction
Author :
Zhao Dongming ; Yang Ping
Author_Institution :
Dept. of Cardiology, Beihua Univ., Jilin, China
fYear :
2011
fDate :
19-22 Aug. 2011
Firstpage :
220
Lastpage :
223
Abstract :
Objectiv to study the anti-oxidation effects of atorvastatin and coenzyme Q10 on heart failure in rats. Methods: After ligating their left anterior descending coronary artery and feeding for 6 weeks, 24 survived rats were randomly divided into sham group (n=6), model group (n=6), atorvastatin group (n=6) and atorvastatin + coenzyme Q10 group (n=6). Following continuous intragastric administration for 5 weeks, hemodynamic parameters, heart weight/body weight (HW/BW), left ventricular heart weight/body weight (LVHW/BW), serum superoxide dismutase (SOD) activity and malondialdehyde (MDA) level were measured for rats. UCP2 mRNA expression levels were determined by RT-PCR in non-infarcted myocardium. Results: Atorvastatin combined with coenzyme Q10 can significantly increase ±dp/dtmax and SOD activity, and reduce left ventricular systolic pressure (LVSP), left ventricular end-diastolic pressure (LVEDP), cardiac hypertrophy index, serum MDA levels and UCP2 mRNA expression levels (P<;0.05~0.001), but had no significant effect on heart rate (HR), systolic blood pressure (SBP) and diastolic blood pressure (DBP) (P>;0.05). Conclusion: Atorvastatin combined with coenzyme Q10 can down-regulate UCP2 mRNA expression levels in myocardial cells for rats with heart failure after myocardial infarction and improve energy metabolism in ventricular remodeling of heart failure via anti-oxidation effects.
Keywords :
biochemistry; blood vessels; cardiology; cellular biophysics; diseases; enzymes; genetics; haemodynamics; macromolecules; molecular biophysics; UCP2 mRNA expression levels; antioxidation effects; atorvastatin group; atorvastatin-coenzyme Q10 effects; cardiac hypertrophy index; continuous intragastric administration; coronary artery; energy metabolism; heart failure; hemodynamic parameters; left anterior; left ventricular end-diastolic pressure; left ventricular heart weight-body weight; left ventricular systolic pressure; malondialdehyde level; myocardial cells; myocardial infarction; noninfarcted myocardium; serum MDA levels; serum superoxide dismutase activity; time 5 week; time 6 week; uncoupling protein 2 gene expression; ventricular remodeling; Arteries; Blood; Heart; Myocardium; Proteins; Rats; Atorvastatin; coenzyme Q10; heart failure; uncoupling protein 2 (UCP2);
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Human Health and Biomedical Engineering (HHBE), 2011 International Conference on
Conference_Location :
Jilin
Print_ISBN :
978-1-61284-723-8
Type :
conf
DOI :
10.1109/HHBE.2011.6027938
Filename :
6027938
Link To Document :
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