Experimental hypercholesterolemia induces ultrastructural changes in the elastic laminae of rabbit aortic valve

被引:12
作者
Kwon, HM [1 ]
Lee, BK [1 ]
Kim, D [1 ]
Hong, BK [1 ]
Byun, KH [1 ]
Kna, JS [1 ]
Kim, IJ [1 ]
Oh, SH [1 ]
Kim, HS [1 ]
机构
[1] Yonsei Univ, Coll Med, Yongdong Severance Hosp, Dept Internal Med,Cardiol Div, Seoul 135270, South Korea
关键词
aortic valve; hypercholesterolemia; confocal microscopy; matrix metalloproteinase;
D O I
10.3349/ymj.1998.39.4.345
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atherosclerosis is the most severe problem in the high-pressure systemic circulation and similar changes also occur in the high-pressure loading valve. This study was designed to test the hypothesis that early atherosclerosis, induced by a high cholesterol diet in rabbits, is characterized by significant ultrastructural change in the elastic laminae of the aortic valve. However, it is not known whether this process is also taking place in the cardiac valve at the early stage of atherosclerosis. Animals were fed either a high cholesterol diet (n=5) or a control diet (n=5) for 10 similar to 12 weeks Histologic analysis demonstrated that subendothelial thickening and foam-cell infiltration were evident in the arterialis of aortic valves. Confocal microscopy revealed an altered pattern characterized by fragmentation and disorganization of the arterialis elastic laminae of hypercholesterolemic valves. Computerized digital analysis of the images obtained by confocal scanning microscopy demonstrated that compared to normal valves, the arterialis elastic laminae of hypercholesterolemic valves decreased in percentage of their elastin content (29.03+/-1.10% vs. 42.94+/-1.35%, p=0.023). Immunohistochemical staining for matrix metalloproteinase-3 (MMP-3) revealed MMP-3 immunoreactivity was increased in hypercholesterolemic valves, predominantly in the arterialis. This study demonstrated that early atherosclerosis, induced by a high cholesterol diet in rabbits, is characterized by significant ultrastructural change in the elastic laminae of the aortic valve. The arterialis endothelium of the aortic valve may be a more atherosclerosis-prone area compared with the ventricularis. The presence of ultrastructural defect in the elastic laminae may play a role in chronic degenerative change and a resultant valvular dysfunction.
引用
收藏
页码:345 / 354
页数:10
相关论文
共 32 条
[1]  
ALLAIN CC, 1974, CLIN CHEM, V20, P470
[2]   TISSUE INHIBITOR OF METALLOPROTEASES (TIMP) IS MATRIX ASSOCIATED IN AORTIC TISSUE - REPORT OF A RADIOIMMUNOASSAY [J].
BROPHY, CM ;
MARKS, WH ;
REILLY, JM ;
TILSON, MD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 167 (03) :898-903
[3]   Valvular heart disease [J].
Carabello, BA ;
Crawford, FA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (01) :32-41
[4]   SMOOTH-MUSCLE CELL ELASTASE, ATHEROSCLEROSIS, AND ABDOMINAL AORTIC-ANEURYSMS [J].
COHEN, JR ;
SARFATI, I ;
DANNA, D ;
WISE, L ;
HUNTER, G ;
MANNICK, JA ;
MACKENZIE, JW ;
DARLING, RC .
ANNALS OF SURGERY, 1992, 216 (03) :327-332
[5]   Fluorescence and confocal laser scanning microscopy imaging of elastic fibers in hematoxylin-eosin stained sections [J].
deCarvalho, HF ;
Taboga, SR .
HISTOCHEMISTRY AND CELL BIOLOGY, 1996, 106 (06) :587-592
[6]   INCREASED EXPRESSION OF MATRIX METALLOPROTEINASES AND MATRIX-DEGRADING ACTIVITY IN VULNERABLE REGIONS OF HUMAN ATHEROSCLEROTIC PLAQUES [J].
GALIS, ZS ;
SUKHOVA, GK ;
LARK, MW ;
LIBBY, P .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2493-2503
[7]   CORRELATION BETWEEN LIPOPROTEIN(A) AND AORTIC-VALVE SCLEROSIS ASSESSED BY ECHOCARDIOGRAPHY (THE JMS CARDIAC ECHO AND COHORT STUDY) [J].
GOTOH, T ;
KURODA, T ;
YAMASAWA, M ;
NISHINAGA, M ;
MITSUHASHI, T ;
SEINO, Y ;
NAGOH, N ;
KAYABA, K ;
YAMADA, S ;
MATSUO, H ;
HOSOE, M ;
ITOH, Y ;
KAWAI, T ;
IGARASHI, M ;
SHIMADA, K .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 76 (12) :928-932
[8]  
GROSS L, 1931, AM J PATHOL, V27, P420
[9]   LOCALIZATION OF STROMELYSIN GENE-EXPRESSION IN ATHEROSCLEROTIC PLAQUES BY INSITU HYBRIDIZATION [J].
HENNEY, AM ;
WAKELEY, PR ;
DAVIES, MJ ;
FOSTER, K ;
HEMBRY, R ;
MURPHY, G ;
HUMPHRIES, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (18) :8154-8158
[10]  
HERRON GS, 1986, J BIOL CHEM, V261, P2814