Cardiomyocyte cyclooxygenase-2 influences cardiac rhythm and function.

نویسندگان

  • Dairong Wang
  • Vickas V Patel
  • Emanuela Ricciotti
  • Rong Zhou
  • Mark D Levin
  • Ehre Gao
  • Zhou Yu
  • Victor A Ferrari
  • Min Min Lu
  • Junwang Xu
  • Hualei Zhang
  • Yiqun Hui
  • Yan Cheng
  • Nataliya Petrenko
  • Ying Yu
  • Garret A FitzGerald
چکیده

Nonsteroidal anti-inflammatory drugs selective for inhibition of COX-2 increase heart failure and elevate blood pressure. The COX-2 gene was floxed and crossed into merCremer mice under the alpha-myosin heavy-chain promoter. Tamoxifen induced selective deletion of COX-2 in cardiomyocytes depressed cardiac output, and resulted in weight loss, diminished exercise tolerance, and enhanced susceptibility to induced arrhythmogenesis. The cardiac dysfunction subsequent to pressure overload recovered progressively in the knockouts coincident with increasing cardiomyocyte hypertrophy and interstitial and perivascular fibrosis. Inhibition of COX-2 in cardiomyocytes may contribute to heart failure in patients receiving nonsteroidal anti-inflammatory drugs specific for inhibition of COX-2.

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 106 18  شماره 

صفحات  -

تاریخ انتشار 2009