Inhibition of MMP-2 activation and release as a novel mechanism for HDL-induced cardioprotection

FEBS Lett. 2006 Oct 30;580(25):5974-8. doi: 10.1016/j.febslet.2006.10.006. Epub 2006 Oct 12.

Abstract

High density lipoproteins (HDL) protect the heart against ischemia/reperfusion (I/R) injury, and matrix metalloproteinase-2 (MMP-2) directly contributes to cardiac contractile dysfunction after I/R. To investigate the possible involvement of MMP-2 inhibition in HDL-mediated cardioprotection, isolated rat hearts underwent 20 min of low-flow ischemia and 30 min of reperfusion. Plasma-derived and synthetic HDL attenuated the I/R-induced cardiac MMP-2 activation and release in a dose-dependent way. The attenuation of I/R-induced MMP-2 activation by HDL correlated with the reduction of post-ischemic contractile dysfunction and cardiomyocyte necrosis. These results indicate prevention of MMP-2 activation as a novel mechanism for HDL-mediated cardioprotection.

MeSH terms

  • Animals
  • Base Sequence
  • DNA, Complementary / genetics
  • Enzyme Activation / drug effects
  • Humans
  • In Vitro Techniques
  • Lipid Peroxides / metabolism
  • Lipoproteins, HDL / pharmacology*
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase Inhibitors*
  • Myocardial Reperfusion Injury / enzymology*
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / prevention & control*
  • Myocardium / metabolism
  • Rats
  • Reactive Oxygen Species / metabolism

Substances

  • DNA, Complementary
  • Lipid Peroxides
  • Lipoproteins, HDL
  • Matrix Metalloproteinase Inhibitors
  • Reactive Oxygen Species
  • Matrix Metalloproteinase 2