FIZZ1在载脂蛋白E基因敲除小鼠动脉粥样硬化发生发展中的可能作用及机制
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Effects and Mechanisms of FIZZ1 on Atherogenesis in ApoE-knockout Mice
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    目的探讨FIZZ1在载脂蛋白E基因敲除小鼠动脉粥样硬化发生发展中的可能作用及机制。方法20只8周龄载脂蛋白E基因敲除小鼠随机分为模型组和罗格列酮组,另取10只8周龄野生型C57/BL小鼠作为对照组,3组均饲喂普通饮食,罗格列酮组给予罗格列酮10 mg/(kg.d),12周后获取静脉血和主动脉标本。静脉血用于检测血脂和高敏C反应蛋白。部分主动脉标本用于病理学检测动脉粥样硬化病变。其余标本用于免疫组织化学和RT-PCR检测FIZZ1的表达。结果模型组和罗格列酮组的血脂水平均显著高于对照组(P<0.05),前二组之间差异无显著性。高敏C反应蛋白在前两组水平均较对照组高(P<0.05),其中罗格列酮组低于模型组。罗格列酮组和模型组主动脉均形成明显的动脉粥样硬化斑块,罗格列酮干预组病变较模型组轻。免疫组织化学和RT-PCR结果发现,对照组FIZZ1没有表达,模型组和罗格列酮组均有表达,且模型组表达量较罗格列酮组显著增高。结论FIZZ1在动脉粥样硬化病变中表达增高,罗格列酮干预后表达可降低,伴随着动脉粥样硬化斑块面积缩小,提示罗格列酮具有抗动脉粥样硬化作用,其机制与调脂无关,可能与其抑制炎症反应有关。

    Abstract:

    Aim To observe the expression of found in inflammatory zone1(FIZZ1) in aortic atherosclerosis lesion and the interventional effect of rosiglitazone in apolipoprotein E-knockout mice. Methods Eight-week-old apoE knockout mice were divided into atherosclerosis(As) group(n=10) and rosiglitazone group(n=10).Wildtype C57/BL mice(n=10) were used as normal control group(n=10).All mice were fed with normal chow diet.In addition to normal diet,rosiglitazone group received rosiglitazone 10 mg/(kg·g) of body weight.After 12 weeks,aorta were used for histomorphometric analysis of atherosclerosis lesion,immunohistochemistry and RT-PCR for the expression of FIZZ1.Vessel bloods were collected for plAsma lipid and high sensitive-CRP(hs-CRP). Results There is no significant difference in blood lipid level between As group and rosiglitazone group.The hs-CRP level in As group is significantly higher than that in rosiglitazone group.Histomorphometric analysis showed that the area of atherosclerosis plaque in As group was significantly bigger than that in rosiglitazone group.Immunohistochemistry and RT-PCR showed that the expression of FIZZ1 in As group were higher than that in rosiglitazone group. Conclusion The expression of FIZZ1 in atherosclerosis lesion was observed.Rosiglitazone can decrease hs-CRP level,reduce the expression of FIZZ1 in aortic atherosclerosis lesion.It is not related to modulation of blood lipid that rosiglitazone inhibits the development of aortic atherosclerosis.Anti-inflammation is a potential mechanism.

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高凌云,李福平,何作云,牟娇. FIZZ1在载脂蛋白E基因敲除小鼠动脉粥样硬化发生发展中的可能作用及机制[J].中国动脉硬化杂志,2008,16(8):619~622.

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  • 收稿日期:2007-07-13
  • 最后修改日期:2008-03-02
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