期刊文献+

NADPH氧化酶Nox4调控非诺贝特的抗高血压心肌肥大效应 被引量:2

NADPH Oxidase Nox4 Regulates the Protective Effect of Fenofribate Against Cardiac Hypertrophy
下载PDF
导出
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。 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 hypertensioninduced cardiac hypertrophy. It will provide further theoretical and experimental support for fenofribate curing hypertension- induced myocardial hypertrophy.
出处 《中国动脉硬化杂志》 CAS 北大核心 2016年第6期557-560,共4页 Chinese Journal of Arteriosclerosis
基金 广东省自然科学基金(2015A030310076)
关键词 非诺贝特 心肌肥大 NADPH氧化酶Nox4 Fenofribate Cardiac Hypertrophy NADPH Oxidase Nox4
  • 相关文献

参考文献12

  • 1梁伟杰,陈景福,宋明才,李健仪,郑东诞,张稳柱,潘玩莹,冯鉴强,廖新学.活性氧与ATP敏感性钾通道的相互作用参与高糖对H9c2心肌细胞的损伤[J].中国动脉硬化杂志,2015,23(11):1081-1088. 被引量:6
  • 2Byrne JA, Grieve D J, Bendall JK, et al. Contrasting roles of NADPH oxidase isofonns in pressure-overload versus angiotensin II-induced cardiac hypertrophy[J]. Circ Res, 2003, 93(9): 802-805. 被引量:1
  • 3Maytin M, Siwik DA, Ito M, et al. Pressure overloadinduced myocardial hypertrophy in mice does not require gp91phox [ J]. Circulation, 2004, 109 (9): 1 168-171. 被引量:1
  • 4Zhao QD, Viswanadhapalli S, Williams P, et al. NADPH oxidase 4 induces cardiac fibrosis and hypertrophy through activating Akt/mTOR and NFKB signaling pathways[J]. Circulation, 2015, 131(7): 643-655. 被引量:1
  • 5Kuroda J, Ago T, Matsushima S, et al. NADPH oxidase 4 (Nox4) is a major source of oxidative stress in the failing heart [ J ]. Prec Nat1 Acad Sci USA, 2010, 107(35) : 15 565-570. 被引量:1
  • 6Shouji Matsushima, Junya Kuroda, Tetsuro Ago, et al. Increased oxidative stress in the nucleus caused by Nox4 mediates oxidation of HDAC4 and cardiac hypertrophy[J]. Circ Res, 2013, 112(4): 651-663. 被引量:1
  • 7Ahhurwi HN, Elshenawy OH, E1-Kadi AO. Fenofibrate modulates cytochreme P450 and arachidonic acid metabolism in the heart and protects against isoproterenol-induced cardiac hypertrophy[J]. J Cardiovasc Pharmacol, 2014, 63 (2) : 167-177. 被引量:1
  • 8Zou J, Le K, Xu S, et al. Fenofibrate ameliorates cardiac hypertrophy by activation of perexisome proliferator-activated receptor-c~ partly via preventing p65-NFKB binding to NFATc4[J]. Mol Cell Endocrinol, 2013, 370 (1-2): 103-112. 被引量:1
  • 9Zeng SY, Chen X, Chen SR, et al. Upregulation of Nox4 promotes angiotensin I1-induced epidermal growth factor receptor activation and subsequent cardiac hypertrophy by increasing ADAM 17 expression[ .l ]. Can J Cardial, 2013, 29(10) : 1 310-319. 被引量:1
  • 10Jia Z, Xue R, Liu G, et al. hmgbl is involved in the protective effect of the ppara aganist fenofibrate against cardiac hypertrophy[ J]. PPAR Res, 2014, 2014:541 -394. 被引量:1

二级参考文献12

  • 1Wenming Xu,Wen Wu,Jingfu Chen,Runmin Guo,Jiancong Lin,Xinxue Liao,Jianqiang Feng.??Exogenous hydrogen sulfide protects H9c2 cardiac cells against highglucose-induced injury by inhibiting the activities of the p38 MAPK and ERK1/2pathways(J)International Journal of Molecular Medicine . 2013 (4) 被引量:2
  • 2Xiao-Dong Zhuang,Xun Hu,Ming Long,Xiao-Bian Dong,Dong-Hong Liu,Xin-Xue Liao.??Exogenous hydrogen sulfide alleviates high glucose-induced cardiotoxicity via inhibition of leptin signaling in H9c2 cells(J)Molecular and Cellular Biochemistry . 2014 (1-2) 被引量:2
  • 3Bian JS,Yong QC,Pan TT,et al.Role of hydrogen sulfide in the cardioprotection caused by ischemic preconditioning in the rat heart and cardiac myocytes. Journal of Pharmacology and Experimental Therapeutics . 2006 被引量:1
  • 4Hiroyuki Kinoshita,Naoyuki Matsuda,Hikari Kaba,Noboru Hatakeyama,Toshiharu Azma,Katsutoshi Nakahata,Yasuhiro Kuroda,Kazuaki Tange,Hiroshi Iranami,Yoshio Hatano.??Roles of Phosphatidylinositol 3-Kinase-Akt and NADPH Oxidase in Adenosine 5′-Triphosphate–Sensitive K+ Channel Function Impaired by High Glucose in the Human Artery(J)Hypertension . 2008 (3) 被引量:1
  • 5Jingfu Chen,Hailiang Mo,Runmin Guo,Qiong You,Ruina Huang,Keng Wu.??Inhibition of the leptin-induced activation of the p38 MAPK pathwaycontributes to the protective effects of naringin against high glucose-inducedinjury in H9c2 cardiac cells(J)International Journal of Molecular Medicine . 2014 (3) 被引量:1
  • 6Hossein Ardehali,Brian O’Rourke.??Mitochondrial K ATP channels in cell survival and death(J)Journal of Molecular and Cellular Cardiology . 2005 (1) 被引量:1
  • 7Tanya M. Bisseling,Marieke G. Versteegen,Selina van der Wal,Jenny J.H. Copius Peereboom-Stegeman,Joop M.P.M. Borggreven,Eric A.P. Steegers,Jeroen A.W.M. van der Laak,Frans G.M. Russel,Paul Smits.??Impaired K ATP channel function in the fetoplacental circulation of patients with type 1 diabetes mellitus(J)American Journal of Obstetrics and Gynecology . 2005 (3) 被引量:1
  • 8Noma A.ATP-regulated K+ channels in cardiac muscle. Nature . 1983 被引量:1
  • 9Nichols C G,Lederer W J.Adenosine triphosphate-sensitive potassium channels in the cardiovascular system. The American journal of physiology . 1991 被引量:1
  • 10刘付贞,潘德茂,陈景福,郭润民,闫海,田丽红,吴铿.柚皮苷抗高糖诱导的心肌细胞损伤作用与抑制STAT3通路有关[J].中国动脉硬化杂志,2014,22(4):345-350. 被引量:7

共引文献5

同被引文献4

引证文献2

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部