复合因素致大鼠实验性动脉粥样硬化模型建立  被引量:3

Establishment of experimental atherosclerotic model in rats with multi-factor

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作  者:傅剑云[1] 夏勇[1] 孟佳[1] 郑云燕[1] 蔡德雷[1] 周矗[2] 

机构地区:[1]浙江省疾病预防控制中心,杭州310051 [2]温州医学院生命科学学院,杭州310053

出  处:《中国卫生检验杂志》2011年第1期16-20,共5页Chinese Journal of Health Laboratory Technology

基  金:浙江省科技计划项目(2007F80014)

摘  要:目的:建立适合于心血管疾病研究的复合因素致大鼠动脉粥样硬化模型。方法:健康SD雄性大鼠,分为10组,空白对照组、高脂对照组、L-met(低)组和L-met(高)组、高脂+L-met(低)组(4、6、8周)、高脂+L-met(高)组(4、6、8周)。检测血清TC、TG、HDL,检测血浆同型半胱氨酸(Hcy)、单核细胞趋化因子1(MCP-1)和白介素6(IL-6),分离各组大鼠主动脉弓,置于10%中性福尔马林中固定,作HE染色。结果:试验后,高脂对照组和高脂+L-met(低、高)(4、6、8周)组大鼠血清TC水平均明显增高;高脂对照组和高脂+L-met(低、高)(4周)组大鼠血清TG水平均明显增高;高脂对照组、L-met(低、高)和高脂+L-met(低、高)(4、6、8周)组大鼠血浆Hcy水平均明显增高;L-met(低、高)、高脂+L-met(低)(6、8周)组和高脂+L-met(高)(4、6、8周)大鼠血浆MCP-1水平均明显增高,同空白对照组相比P<0.05。L-met(低)组和高脂+L-met(低)组(4周)大鼠可见早期动脉粥样硬化改变,L-met(高)组、高脂+L-met(低)组(6、8周)和高脂+L-met(高)组(4、6周)大鼠可见中、晚期AS病理改变,高脂+L-met(高)组(8周)大鼠则出现晚期动脉粥样硬化改变。结论:通过L-met灌胃,联合应用高脂饲料喂养的方法可建立较理想的动脉粥样硬化模型。Objective:To establish a kind of Multi-factor of rat atherosclerosis model suitable for research of cardiovascular diseases.Methods: Healthy male SD rats were randomly divided into 10 groups according to basal TC: control group,high lipid group,L-met(L)group,L-met(H)group,high lipid + L-met(L)group(4,6,8W) group,high lipid + L-met(H)group(4,6,8W) group.Serum lipid and plasma Hcy,MCP-1,IL-6 were determined.Thoracic aortae were isolated and prepared for pathologic examinations.Results: The levels of serum TC in high lipid group and high lipid + L-met(L,H)groups(4,6,8W) were obviously higher than those in control group(P0.05),the levels of serum TG in high lipid group and high lipid + L-met(L,H)groups(4W) higher than those in control group(P0.05),the levels of plasma Hcy in high lipid group and all experimental groups higher than those in control group(P0.05),the levels of plasma MCP-1 in high lipid group and all experimental groups except for high lipid + L-met(L)groups(4W) group higher than those in control group(P0.05).Pathologic examinations showed that there were early aortae atherosclerotic changes in L-met(L)group and high lipid + L-met(L)groups(4W);middle and later atherosclerotic changes in L-met(H)group and high lipid + L-met(L)groups(6,8W) and high lipid + L-met(H)groups(4,6W);later atherosclerotic changes in high lipid + L-met(H)groups(8W) groups.Conclusion: Ideal atherosclerotic model in rats can be established by treating rats with L-met accompanied by an high lipid diet.

关 键 词:动脉硬化模型 高脂 L-甲硫氨酸(L-met) 大鼠 

分 类 号:R543.5[医药卫生—心血管疾病]

 

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