Effect of nitric oxide on the antiatherogenic course of atorvastatin
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Effect of nitric oxide on the antiatherogenic course of atorvastatin
Journal of Chongqing Medical UniversityVol. 40, Issue 9, Pages: 1232-1235(2015)
作者机构:
泸州医学院附属医院心内科,泸州,646000
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Published:2015,
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Liu Xing, Ma Dongming, Zhu Bo, et al. Effect of nitric oxide on the antiatherogenic course of atorvastatin. [J]. Journal of Chongqing Medical University 40(9):1232-1235(2015)
DOI:
Liu Xing, Ma Dongming, Zhu Bo, et al. Effect of nitric oxide on the antiatherogenic course of atorvastatin. [J]. Journal of Chongqing Medical University 40(9):1232-1235(2015)DOI:
Effect of nitric oxide on the antiatherogenic course of atorvastatin
Objective:To investigate antiatherosclerosis effect of atorvastatin in atherosclerosis model of SD rats,and to explore effect of nitric oxide in this course. Methods:Totally 60 male SD rats were divided into 4 groups randomly:control group,high-fat(HF) group,atorvastatin(ATV) group,and ATV+ N’-nitro-L-arginine-methyl ester hydrochloride(L-NAME) group. After being fed a high-fat diet,the rats were treated with ATV and ATV combined with L-NAME from 13 to 15 weeks,respectively. Pathologic changes of aortic arch were observed. Serum lipid level was determined. Furthermore,nitric oxide(NO),total nitric oxide synthase(T-NOS),endothelial nitric oxide synthase(eNOS) and eNOSmRNA were also determined. Results:The classical atherosclerotic lesions were fund in HF group and ATV+ L-NAME group,not in control group;serum lipid in the HF group was significantly altered(P<0.05). Levels of serum NO,eNOS,vitality of serous T-NOS and mRNA levels of eNOS in the HF group were decreased(P<0.05). Compared with those of HF group,atherosclerotic lesions were ameliorated in the ATV group. Serum lipid in the ATV group were significantly decreased(P<0.05). Serum NO,eNOS,vitality of serous T-NOS and mRNA levels of eNOS in the ATV group were elevated(P<0.05). Compared with those in ATV group,serum lipid levels in the ATV+ L-NAME group were significantly elevated(P<0.05);serum NO,eNOS,and vitality of serous T-NOS in the ATV+L-NAME group were decreased(P<0.05). Conclusion:Atorvastatin significantly enhances the activity of serum nitric oxide system. The blockage of nitric oxide pathway significantly bates antiatherosclerosis of atorvastatin.