INCREASED PLASMA-IMMUNOREACTIVE ENDOTHELIN-1 CONCENTRATION IN HYPERCHOLESTEROLEMIC RATS

被引:39
作者
HORIO, T [1 ]
KOHNO, M [1 ]
MURAKAWA, K [1 ]
YASUNARI, K [1 ]
YOKOKAWA, K [1 ]
UEDA, M [1 ]
TAKEDA, T [1 ]
机构
[1] OSAKA CITY UNIV, SCH MED, DEPT PATHOL, ABENO KU, OSAKA 545, JAPAN
关键词
HYPERCHOLESTEROLEMIA; ENDOTHELIN-1; CLINOFIBRATE; RATS;
D O I
10.1016/0021-9150(91)90065-B
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study examined the influence of hypercholesterolemia on the concentration of plasma immunoreactive (ir) endothelin-1 in rats. Plasma ir-endothelin-1, total cholesterol, triglycerides, and lipoprotein fraction concentrations were measured in three groups of rats; ie, fed a standard diet, a high cholesterol diet, or a high cholesterol diet supplemented with the antihypercholesterolemic drug clinofibrate for 4 and 8 weeks. In the rats fed cholesterol for 8 weeks, morphological changes in thoracic and abdominal aortas were examined. Plasma total cholesterol, low density lipoprotein (LDL), very low density lipoprotein (VLDL) and ir-endothelin-1 concentrations increased significantly in the cholesterol-fed rats after both 4 and 8 weeks. In the clinofibrate-treated rats, these lipid parameters and plasma ir-endothelin-1 levels after 4 and 8 weeks were significantly lower than in the cholesterol-fed rats. The plasma ir-endothelin-1 concentration was correlated with plasma total cholesterol, LDL, and VLDL concentrations in the three study groups after 4 and 8 weeks. Morphologically, neither foam cell formation nor intimal thickening was observed in rats fed the high cholesterol diet for 8 weeks. These observations indicate that hypercholesterolemia without atherosclerosis elevates the plasma ir-endothelin-1 level in rats. The observed increase in plasma ir-endothelin-1 associated with hypercholesterolemia may play a role in the initiation or development of atherosclerotic vascular lesions.
引用
收藏
页码:239 / 246
页数:8
相关论文
共 39 条
[1]   LOW-DENSITY LIPOPROTEINS INHIBIT ENDOTHELIUM-DEPENDENT RELAXATION IN RABBIT AORTA [J].
ANDREWS, HE ;
BRUCKDORFER, KR ;
DUNN, RC ;
JACOBS, M .
NATURE, 1987, 327 (6119) :237-239
[2]  
ARENDT RM, 1990, AM J HYPERTENS, V3, pA93
[3]   LOW-DENSITY LIPOPROTEIN CAUSES GENERAL CELLULAR ACTIVATION WITH INCREASED PHOSPHATIDYLINOSITOL TURNOVER AND LIPOPROTEIN CATABOLISM [J].
BLOCK, LH ;
KNORR, M ;
VOGT, E ;
LOCHER, R ;
VETTER, W ;
GROSCURTH, P ;
QIAO, BY ;
POMETTA, D ;
JAMES, R ;
REGENASS, M ;
PLETSCHER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (03) :885-889
[4]   GROWTH-FACTOR ACTIVITY OF ENDOTHELIN ON VASCULAR SMOOTH-MUSCLE [J].
BOBIK, A ;
GROOMS, A ;
MILLAR, JA ;
MITCHELL, A ;
GRINPUKEL, S .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (03) :C408-C415
[5]  
BOULANGER CM, 1990, J VASC MED BIOL, V2, P185
[6]   IMMUNOREACTIVE ENDOTHELIN IN HUMAN-PLASMA - MARKED ELEVATIONS IN PATIENTS IN CARDIOGENIC-SHOCK [J].
CERNACEK, P ;
STEWART, DJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 161 (02) :562-567
[7]   LOSS OF SELECTIVE ENDOTHELIAL-CELL VASOACTIVE FUNCTIONS CAUSED BY HYPERCHOLESTEROLEMIA IN PIG CORONARY-ARTERIES [J].
COHEN, RA ;
ZITNAY, KM ;
HAUDENSCHILD, CC ;
CUNNINGHAM, LD .
CIRCULATION RESEARCH, 1988, 63 (05) :903-910
[8]  
COLLINS T, 1987, AM J PATHOL, V126, P7
[9]   THE OBLIGATORY ROLE OF ENDOTHELIAL-CELLS IN THE RELAXATION OF ARTERIAL SMOOTH-MUSCLE BY ACETYLCHOLINE [J].
FURCHGOTT, RF ;
ZAWADZKI, JV .
NATURE, 1980, 288 (5789) :373-376
[10]   AN ENDOTHELIAL CELL-DERIVED GROWTH-FACTOR [J].
GAJDUSEK, C ;
DICORLETO, P ;
ROSS, R ;
SCHWARTZ, SM .
JOURNAL OF CELL BIOLOGY, 1980, 85 (02) :467-472