Objectives To investigate effects of atorvastatin on methylation status of bcl-2 gene promoter and mRNA expression of bcl-2 in aortic tissue of hyperlipidaemia Wistar rats. Methods 66 Wistar rats were equally randomised into three groups: control group, hyperlipidaemia group and hyperlipoidaemia rat with atorvastatin group. The rats in control group were fed a normal chaw, and the other groups were fed a chaw formula as designed for 12 weeks. From the 12th week gavage experiment, after 4 weeks

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... f heart blood was then drawn for detection of serum cholesterol, triglyceride, low density lipoprotein-cholesterol, high density lipoprotein-cholesterol; aortic nucleoprotein was extracted for detection of DNA methyltransferase activity. The methylation specific polymerase chain reaction (MSP) method was used to detect bcl-2 gene methylation in aortic tissue of control group, hyperlipidemia group and hyperlipoidemia rat with atorvastatin group. The expression of bcl-2 mRNA in aortic tissue of control group and hyperlipidaemia group Wistar rats was detected by real-time quantitative polymerase chain reaction. Results A high-fat diet for 12 weeks is sufficient to induce hyperlipidaemia; Atorvastatin supplementation to the rats fed the highfat diet prevented an elevation total cholesterol (TC), triglyceride (TG), low density lipoprotein-cholesterol (LDL-C) and increase high density lipoprotein-cholesterol (HDL-C) levels in the serum ( p<0.05) and morphological changes in the thoracic aorta. Compared with the control group, hyperlipidaemia group significantly increased DNA methyltransferase activity and methylation status of bcl-2 gene promoter ( p<0.05), the expression of bcl-2 mRNA was decreased in hyperlipidaemia groups ( p<0.05). Compared with the hyperlipidaemia group, atorvastatin group significantly decreased DNA methyltransferase activity and methylation status of bcl-2 gene promoter ( p<0.05), the expression of bcl-2 mRNA was increased in hyperlipidaemia groups ( p<0.05).