NADPH氧化酶Nox4调控非诺贝特的抗高血压心肌肥大效应
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(1.广东省第二人民医院,广东省广州市510317;2.中山大学,广东省广州市510000;3.广州医科大学附属第三医院,广东省广州市510000)

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曾泗宇,博士,主管药师,主要从事心血管重构的机制研究及药物研发,E-mail为cosmo81 @qq.com。严鹏科,博士,教授,主要从事动脉粥样硬化以及心血管重构的机制研究,E-mail为438726802 @qq.com。

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广东省自然科学基金(2015A030310076)


NADPH Oxidase Nox4 Regulates the Protective Effect of Fenofribate Against Cardiac Hypertrophy
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Affiliation:

1.Guangdong No.2 Provicial People’s Hospital, Guangzhou, Guangdong 510317;2.Sun Yat-sen University, Guangzhou, Guangdong 510000;3.The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong 510000)

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    摘要:

    目的 拟阐明NADPH氧化酶Nox4与非诺贝特抗高血压心肌肥大效应的关系。方法 构建腹主动脉缩窄(abdominal aorta coarctation,AAC)诱导的高血压大鼠模型,观察非诺贝特对高血压大鼠左心室肥大的影响。结果 非诺贝特可显著抑制AAC高血压大鼠左心室肥大。与假手术组比较,AAC组左心室中NADPH氧化酶Nox4蛋白和mRNA水平均显著增加;与AAC组比较,非诺贝特剂量依赖性降低AAC高血压大鼠左心室中NADPH氧化酶Nox4蛋白和mRNA水平。结论 降低NADPH氧化酶Nox4表达可能是非诺贝特发挥抗高血压心肌肥大效应的重要机制。

    Abstract:

    Aim To elucidate the relation between NADPH oxidase Nox4 and the protective effect of fenofribate against cardiac hypertrophy. Methods Abdominal aorta coarctation (AAC)-induced hypertensive rats were constructed to observe the effect of fenofribate on left ventricular hypertrophy. Results Fenofribate could inhibit left ventricular hypertrophy in AAC-induced hypertensive rats. Compared with sham group, the mRNA and protein levels of NADPH oxidase Nox4 were significantly elevated in left ventricular tissue of AAC group; compared with AAC group, fenofribate reduced the mRNA and protein levels of NADPH oxidase Nox4 in left ventricular tissue in a dose-dependent manner.Conclusion Reducing NADPH oxidase Nox4 expression could be a crucial mechanism of fenofribate against hypertension-induced cardiac hypertrophy. It will provide further theoretical and experimental support for fenofribate curing hypertension- induced myocardial hypertrophy.

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曾泗宇,周长华,兰树敏,卢慧勤,陈燕,严秋江,严鹏科,刘培庆. NADPH氧化酶Nox4调控非诺贝特的抗高血压心肌肥大效应[J].中国动脉硬化杂志,2016,24(6):557~560.

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  • 收稿日期:2015-11-05
  • 最后修改日期:2015-12-24
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  • 在线发布日期: 2016-06-30