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

被引:16
作者
Bellosta, Stefano [1 ]
Gomaraschi, Monica [1 ]
Canavesi, Monica [1 ]
Rossoni, Giuseppe [1 ]
Monetti, Mara [1 ]
Franceschini, Guido [1 ]
Calabresi, Laura [1 ]
机构
[1] Univ Milan, Dept Pharmacol Sci, Ctr E Grossi Paoletti, I-20133 Milan, Italy
关键词
high density lipoproteins; gelatinase A; matrix metalloproteinases; myocardial ischemia; ischemia/reperfusion injury;
D O I
10.1016/j.febslet.2006.10.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:5974 / 5978
页数:5
相关论文
共 22 条
[1]   Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions - A possible peroxidative role for paraoxonase [J].
Aviram, M ;
Rosenblat, M ;
Bisgaier, CL ;
Newton, RS ;
Primo-Parmo, SL ;
La Du, BN .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (08) :1581-1590
[2]   HMG-CoA reductase inhibitors reduce MMP-9 secretion by macrophages [J].
Bellosta, S ;
Via, D ;
Canavesi, M ;
Pfister, P ;
Fumagalli, R ;
Paoletti, R ;
Bernini, F .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (11) :1671-1678
[3]   High-density lipoproteins protect isolated rat hearts from ischemia-reperfusion injury by reducing cardiac tumor necrosis factor-α content and enhancing prostaglandin release [J].
Calabresi, L ;
Rossoni, G ;
Gomaraschi, M ;
Sisto, F ;
Berti, F ;
Franceschini, G .
CIRCULATION RESEARCH, 2003, 92 (03) :330-337
[4]  
Carden DL, 2000, J PATHOL, V190, P255, DOI 10.1002/(SICI)1096-9896(200002)190:3<255::AID-PATH526>3.0.CO
[5]  
2-6
[6]   HIGH-DENSITY-LIPOPROTEIN IS A SCAVENGER OF SUPEROXIDE ANIONS [J].
CHANDER, R ;
KAPOOR, NK .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (07) :1663-1665
[7]   Matrix metalloproteinase-2 contributes to ischemia-reperfusion injury in the heart [J].
Cheung, PY ;
Sawicki, G ;
Wozniak, M ;
Wang, WJ ;
Radomski, MW ;
Schulz, R .
CIRCULATION, 2000, 101 (15) :1833-1839
[8]   Matrix metalloproteinases in vascular remodeling and atherogenesis - The good, the bad, and the ugly [J].
Galis, ZS ;
Khatri, JJ .
CIRCULATION RESEARCH, 2002, 90 (03) :251-262
[9]   BINDING OF TRANSITION-METALS BY APOLIPOPROTEIN-A-I-CONTAINING PLASMA-LIPOPROTEINS - INHIBITION OF OXIDATION OF LOW-DENSITY LIPOPROTEINS [J].
KUNITAKE, ST ;
JARVIS, MR ;
HAMILTON, RL ;
KANE, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (15) :6993-6997
[10]   Ischaemia-reperfusion injury activates matrix metalloproteinases in the human heart [J].
Lalu, MM ;
Pasini, E ;
Schulze, CJ ;
Ferrari-Vivaldi, M ;
Ferrari-Vivaldi, G ;
Bachetti, T ;
Schulz, R .
EUROPEAN HEART JOURNAL, 2005, 26 (01) :27-35