Remodeling after myocardial infarction in humans is not associated with interstitial fibrosis of noninfarcted myocardium

被引:42
作者
Marijianowski, MMH [1 ]
Teeling, P [1 ]
Becker, AE [1 ]
机构
[1] UNIV AMSTERDAM, ACAD MED CTR, DEPT CARDIOVASC PATHOL, NL-1100 DE AMSTERDAM, NETHERLANDS
关键词
D O I
10.1016/S0735-1097(97)00100-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives, This study was specifically designed to evaluate whether noninfarcted hypertrophic myocardium in patients with end stage heart failure after myocardial infarction (MI) is associated with an increase in interstitial fibrous tissue. Background. Postinfarction remodeling consists of complex alterations that involve both infarcted and noninfarcted myocardium, The question arises whether ventricular dysfunction is due to physical events, such as inadequate myocardial hypertrophy to compensate for increased tangential wall stress, or is caused by the development of progressive interstitial fibrosis in noninfarcted myocardium. Methods. Fifteen hearts were obtained as cardiac explants (n = 13) or at autopsy (n = 2) from patients with end stage coronary artery disease, Sixteen normal hearts served as reference hearts, Samples were taken from the left ventricular (LV) wall that contained the infarcted area, the border area and noninfarcted myocardium remote from scar areas, Collagen was quantified biochemically and microdensitophotometrically. Collagen type I and III ratios were analyzed by using the cyanogen bromide method and immunohistochemical staining, followed by microdensitophotometric quantification. Results. In noninfarcted myocardium remote from the scar areas, total collagen levels and collagen type I/III ratios did not differ statistically from those in reference hearts, These observations contrasted with high total collagen content and high collagen type I/III ratios in scar and border areas. Conclusions. Remodeling of LV myocardium after MI in patients with end stage heart failure is not necessarily associated with interstitial fibrosis in noninfected hypertrophic myocardium remote from scar areas, This finding raises questions regarding therapeutic interventions designed to prevent or retard the development of interstitial fibrosis. (C) 1997 by the American College of Cardiology.
引用
收藏
页码:76 / 82
页数:7
相关论文
共 31 条
[11]   HISTOPHOTOMETRIC ESTIMATION OF VOLUME DENSITY OF COLLAGEN AS AN INDICATION OF FIBROSIS IN RAT-LIVER [J].
JAMES, J ;
BOSCH, KS ;
ZUYDERHOUD, FMJ ;
HOUTKOOPER, JM ;
VANGOOL, J .
HISTOCHEMISTRY, 1986, 85 (02) :129-133
[12]  
JAMES J, 1990, LIVER, V10, P1
[13]   PICROSIRIUS STAINING PLUS POLARIZATION MICROSCOPY, A SPECIFIC METHOD FOR COLLAGEN DETECTION IN TISSUE-SECTIONS [J].
JUNQUEIRA, LCU ;
BIGNOLAS, G ;
BRENTANI, RR .
HISTOCHEMICAL JOURNAL, 1979, 11 (04) :447-455
[14]  
KOSTUK WJ, 1973, CIRCULATION, V47, P1174, DOI 10.1161/01.CIR.47.6.1174
[15]   THE PRESENCE OF LARGE AMOUNTS OF TYPE-III COLLAGEN IN BOVINE DENTAL-PULP AND ITS SIGNIFICANCE WITH REGARD TO THE MECHANISM OF DENTINOGENESIS [J].
LECHNER, JH ;
KALNITSKY, G .
ARCHIVES OF ORAL BIOLOGY, 1981, 26 (04) :265-273
[16]   LEFT-VENTRICULAR REMODELING AFTER MYOCARDIAL-INFARCTION - A COROLLARY TO INFARCT EXPANSION [J].
MCKAY, RG ;
PFEFFER, MA ;
PASTERNAK, RC ;
MARKIS, JE ;
COME, PC ;
NAKAO, S ;
ALDERMAN, JD ;
FERGUSON, JJ ;
SAFIAN, RD ;
GROSSMAN, W .
CIRCULATION, 1986, 74 (04) :693-702
[17]   ALTERATION OF COLLAGEN PHENOTYPES IN ISCHEMIC CARDIOMYOPATHY [J].
MUKHERJEE, D ;
SEN, S .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (04) :1141-1146
[18]  
OLLIVIER JP, 1992, AM J CARDIOL, V70, pC27
[19]   VENTRICULAR REMODELING AFTER MYOCARDIAL-INFARCTION - EXPERIMENTAL-OBSERVATIONS AND CLINICAL IMPLICATIONS [J].
PFEFFER, MA ;
BRAUNWALD, E .
CIRCULATION, 1990, 81 (04) :1161-1172
[20]   VENTRICULAR REMODELING - CONSEQUENCES AND THERAPY [J].
SABBAH, HN ;
GOLDSTEIN, S .
EUROPEAN HEART JOURNAL, 1993, 14 :24-29