段宇, 王婷婷, 张明明, 胡建强, 蔺杰, 孙冬冬, 赵志敬. 白藜芦醇通过调节自噬延缓ApoE-/-小鼠动脉粥样硬化进展[J]. 心脏杂志, 2017, 29(3): 259-263,275. DOI: 10.13191/j.chj.2017.0068
    引用本文: 段宇, 王婷婷, 张明明, 胡建强, 蔺杰, 孙冬冬, 赵志敬. 白藜芦醇通过调节自噬延缓ApoE-/-小鼠动脉粥样硬化进展[J]. 心脏杂志, 2017, 29(3): 259-263,275. DOI: 10.13191/j.chj.2017.0068
    DUAN Yu, WANG Ting-ting, ZHANG Ming-ming, HU Jian-qiang, LIN Jie, SUN Dong-dong, ZHAO Zhi-jing. Resveratrol delays the progression of atherosclerosis via inducing autophagy[J]. Chinese Heart Journal, 2017, 29(3): 259-263,275. DOI: 10.13191/j.chj.2017.0068
    Citation: DUAN Yu, WANG Ting-ting, ZHANG Ming-ming, HU Jian-qiang, LIN Jie, SUN Dong-dong, ZHAO Zhi-jing. Resveratrol delays the progression of atherosclerosis via inducing autophagy[J]. Chinese Heart Journal, 2017, 29(3): 259-263,275. DOI: 10.13191/j.chj.2017.0068

    白藜芦醇通过调节自噬延缓ApoE-/-小鼠动脉粥样硬化进展

    Resveratrol delays the progression of atherosclerosis via inducing autophagy

    • 摘要: 目的 探讨白藜芦醇在动脉粥样硬化(AS)进展中的作用和机制。 方法 ApoE-/-小鼠60只随机分为4组(每组15只):对照组、高脂喂养组、白藜芦醇组、高脂喂养+白藜芦醇组。HE染色法观察主动脉斑块病理学改变,生化分析仪检测血脂变化,蛋白质免疫印迹方法(Western blot)测定血管组织微管相关蛋白1轻链3(LC3)以及自噬相关蛋白p62变化。体外培养小鼠巨噬细胞RAW264.7,随机分为4组:对照组、氧化低密度脂蛋白(ox-LDL)损伤组、白藜芦醇组、ox-LDL损伤+白藜芦醇组。TUNEL法检测细胞凋亡,蛋白质Western blot测定自噬相关蛋白LC3Ⅱ、p62的表达。 结果 与高脂喂养组比较,白藜芦醇干预后,AS斑块面积减少(P<0.05),LC3Ⅱ水平上调(P<0.05),p62水平下降(P<0.05),表明白藜芦醇可以诱导自噬;同样,与ox-LDL损伤组比较,白藜芦醇干预后,损伤的巨噬细胞中凋亡水平下降(P<0.05),LC3Ⅱ水平升高(P<0.05),p62水平下降(P<0.05)。 结论 AS进展中会伴随自噬水平的下降,给予白藜芦醇处理后,能够延缓AS进展,其机制可能与白藜芦醇调节自噬能力有关。

       

      Abstract: AIM To investigate the role and mechanism of resveratrol in the progression of atherosclerosis. METHODS Sixty ApoE-/- mice were randomly divided into four groupscontrol, high-fat diet, resveratrol, high-fat diet+resveratrol. Aortic plaques were observed by hematoxylin-eosin(HE) staining and blood lipids were detected by biochemical analyses. Western blot was performed to detect microtubule-associated protein 1 light chain 3(LC3) and Protein 62/Sequestosome 1(p62) changes. Macrophages(murine RAW 264.7 cells) were randomly divided into four groupscontrol, ox-LDL, resveratrol, ox-LDL+resveratrol. Apoptotic index was examined by TUNEL and expressions of LC3 and p62 were analyzed by Western blot. RESULTS With resveratrol treatment, atherosclerotic plaque area was decreased, LC3 Ⅱ level increased and p62 level decreased(P<0.05). After ox-LDL cultured RAW264.7 cell treatment with resveratrol, apoptosis in RAW264.7 cells decreased(P<0.05). Similarly, LC3 Ⅱ level increased and the p62 level declined(P<0.05). CONCLUSION Progression of atherosclerosis is associated with declining autophagy. Resveratrol may delay the progression of atherosclerosis. The mechanism may be related to the enhancement of autophagy.

       

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