A HMG-CoA reductase inhibitor improved regression of atherosclerosis in the rabbit aorta without affecting serum lipid levels: Possible relevance of up-regulation of endothelial NO synthase mRNA

被引:65
作者
Kano, H [1 ]
Hayashi, T [1 ]
Sumi, D [1 ]
Esaki, T [1 ]
Asai, Y [1 ]
Thakur, NK [1 ]
Jayachandran, M [1 ]
Iguchi, A [1 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Geriatr, Nagoya 4468550, Aichi, Japan
关键词
nitric oxide; hypercholesterolemia; arteriosclerosis; regression; endothelial nitric oxide synthase mRNA;
D O I
10.1006/bbrc.1999.0799
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
We determined the role of Fluvastatin: HMG-CoA reductase inhibitor on the regression of atherosclerosis following removal of dietary cholesterol. Male rabbits fed a 0.5% cholesterol diet for 12 weeks were divided into three groups: A1, hypercholesterolemic; A2, fed a regular diet for an 12 additional weeks; and A3, fed a regular diet with fluvastadin (2 mg/kg/day). Fluvastatin treatment (A3) did not affect serum lipid levels compared with A2. However, it decreased the atherosclerotic area in the aortic arch and decreased total and esterified cholesterol concentrations in the descending aorta. Tone-related basal NO release in the thoracic aorta was larger in A3 than in A2. eNOS mRNA in vessel was determined by competitive RT-PCR Essay. It increased in A1, compared with normal aorta and decreased in A2; however, it did not decrease in A3. This is the first report of a decrease in eNOS mRNA in atherosclerosis after removal of dietary cholesterol and a reversal of it by a HMG-CoA reductase inhibitor, which may contribute to the regression of atherosclerosis. (C) 1999 Academic Press.
引用
收藏
页码:414 / 419
页数:6
相关论文
共 23 条
[1]  
ALLAIN CC, 1974, CLIN CHEM, V20, P470
[2]  
BADIMON JJ, 1990, J CLIN INVEST, V85, P1223
[3]   LOW BASAL AND STIMULATED RELEASE OF NITRIC-OXIDE IN ATHEROSCLEROTIC EPICARDIAL CORONARY-ARTERIES [J].
CHESTER, AH ;
ONEIL, GS ;
MONCADA, S ;
TADJKARIMI, S ;
YACOUB, MH .
LANCET, 1990, 336 (8720) :897-900
[4]  
CREAGER MA, 1990, J CLIN INVEST, V86, P1864
[5]   MOLECULAR MECHANISMS OF NITRIC-OXIDE REGULATION - POTENTIAL RELEVANCE TO CARDIOVASCULAR-DISEASE [J].
DINERMAN, JL ;
LOWENSTEIN, CJ ;
SNYDER, SH .
CIRCULATION RESEARCH, 1993, 73 (02) :217-222
[6]   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
[7]   RESTORATION OF ENDOTHELIUM-DEPENDENT RELAXATION BY DIETARY-TREATMENT OF ATHEROSCLEROSIS [J].
HARRISON, DG ;
ARMSTRONG, ML ;
FREIMAN, PC ;
HEISTAD, DD .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (06) :1808-1811
[8]   PHYSIOLOGICAL CONSEQUENCES OF INCREASED VASCULAR OXIDANT STRESSES IN HYPERCHOLESTEROLEMIA AND ATHEROSCLEROSIS - IMPLICATIONS FOR IMPAIRED VASOMOTION [J].
HARRISON, DG ;
OHARA, Y .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (06) :B75-B81
[9]   ESTROGEN INCREASES ENDOTHELIAL NITRIC-OXIDE BY A RECEPTOR-MEDIATED SYSTEM [J].
HAYASHI, T ;
YAMADA, K ;
ESAKI, T ;
KUZUYA, M ;
SATAKE, S ;
ISHIKAWA, T ;
HIDAKA, H ;
IGUCHI, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 214 (03) :847-855
[10]   BASAL RELEASE OF NITRIC-OXIDE FROM AORTIC RINGS IS GREATER IN FEMALE RABBITS THAN IN MALE RABBITS - IMPLICATIONS FOR ATHEROSCLEROSIS [J].
HAYASHI, T ;
FUKUTO, JM ;
IGNARRO, LJ ;
CHAUDHURI, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (23) :11259-11263