The Effect of Matrix Metalloproteinase Inhibitor for Left Ventricular Remodeling after Myocardial Infarction in a Rabbit Model.
- Author:
Soo Hyun KIM
1
;
Sung Sae HAN
;
Tae Eun JUNG
;
Geu Ru HONG
Author Information
1. Su Thoracic and Cardiovascular Surgical Clinic, Korea.
- Publication Type:Original Article
- Keywords:
Myocardial infarction;
Matrix metalloproteinase;
Left ventricular remodeling
- MeSH:
Blotting, Western;
Capillaries;
Collagen;
Coronary Vessels;
Dilatation;
Heart;
Ligation;
MMPI;
Myocardial Infarction*;
Preoperative Period;
Rabbits;
Ventricular Remodeling*
- From:The Korean Journal of Thoracic and Cardiovascular Surgery
2007;40(5):329-340
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Matrix Metalloproteinase (MMP) inhibition has emerged as a potential therapeutic strategy for the left ventricular dilatation that occurs after myocardial infarction. This study is designed to evaluate which treatment is better for attenuating the left ventricular remodeling via MMP inhibition 1) during the early, short highly MMP producing period of the initial phase or 2) during most of the period of the initial phase after myocardial infarction. MATERIAL AND METHOD: Myocardial infarction was induced by ligation of the left anterior descending coronary artery in rabbits. The experimental group was divided into 3 groups. The myocardial infarction only (MI only) group consisted of 7 cases. The MMP inhibitor administered for 5 days after MI (MMPI 5d) group had 6 cases, and these rabbits were given MMP inhibitor for 5 days after myocardial infarction, beginning with the postoperative first day. MMP inhibitor administered for 9 days (MMPI 9d) group consisted of 5 cases and these rabbits were given MMPI for 9 days the same manner as above. CG2300 was used as a selective MMPI; this is a potent MMP-2 and -9 inhibitor. Two-D echocardiograms were performed on all the groups at the time of preoperative period, the postoperative 1st week, the postoperative 2d week and the postoperative 3d week, and we measured the end-diastolic dimension (EDD), the end-systolic dimension (ESD), and the ejection fraction (EF). RESULT: The echocardiograms generally showed postoperative left ventricular dilatation in the MI only group. The EDD was increased significantly higher in the postoperative 1 week compared to the preoperative value (p<0.05). The ESD was also increased significantly higher in the postoperative 1st week, the postoperative 2d week and the postoperative 3d week compared to the preoperative value (p<0.05). Left ventricular dilatation was noted to be less In the MMPI 9d group than in the MI only and MMPI 5d groups. In the MMPI 9d group, there was no significant change of EF postoperatively compared to the preoperative period. MMP-2 and MMP-9 were measured from the infarcted myocardial tissue at post-MI 4 weeks by performing western blotting and zymography. The changes the of protein expression and activity of MMP-2 and MMP-9 were not significant in the three MI groups and the normal heart group. Histopathologic examination revealed severe collagen deposition in the MI only group. Collagen accumulation was reduced in both the MMPI groups. The MMPI 9d group revealed an increased number of capillaries. CONCLUSION: Left ventricular dilatation developed rapidly after, MI from ligation of the coronary artery and MMPI attenuated the ventricular dilatation. The effect of MMPI seemed to have better a result from its usage during most of the period of the initial phase after myocardial infarction. This suggested that increased neovascularization by MMPI may also contribute to attenuation of the left ventricular remodeling.