Inhibitory effect of fluvastatin at doses insufficient to lower serum lipids on the catheter-induced thickening of intima in rabbit femoral artery

被引:44
作者
Bandoh, T
Mitani, H
Niihashi, M
Kusumi, Y
Ishikawa, J
Kimura, M
Totsuka, T
Sakurai, I
Hayashi, S
机构
[1] SANDOZ TSUKUBA RES INST,DEPT PHARMACOL,TSUKUBA,IBARAKI 30026,JAPAN
[2] NIHON UNIV,SCH MED,DEPT PATHOL 2,ITABASHI KU,TOKYO 173,JAPAN
关键词
balloon catheterization; hyperplasia; HMG-CoA reductase inhibitor;
D O I
10.1016/S0014-2999(96)00573-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The anti-atherosclerotic effect of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors at doses insufficient to lower serum cholesterol was investigated in rabbit femoral artery denuded by balloon catheter. Fluvastatin and pravastatin were given orally at doses of 4 and 8 mg/kg per day, respectively, or 2 weeks after the catheterization. There was little change in serum cholesterol, triglyceride and phospholipid by chronic treatment with the drugs. The cross-sectional area of the intima, expressed as relative values to media (I/M ratio), was increased by the catheterization, showing intimal thickening in the denuded arteries. The I/M ratio was reduced by fluvastatin but not pravastatin; 0.327 +/- 0.060 for control, 0.116 +/- 0.035 for 4 mg/kg fluvastatin, 0.088 +/- 0.027 for 8 mg/kg fluvastatin and 0.22 +/- 0.069 for 8 mg/kg pravastatin. Fluvastatin (8 mg/kg)-induced effect on the I/M ratio, was prevented by the combined administration with 40 mg/kg per day mevalonate, a metabolite in the HMG-CoA reductase pathway. These results suggest that fluvastatin inhibits intimal thickening after catheterization-induced injury through percutaneous transluminal coronary angioplasty (PTCA) and that the inhibition is presumably attributed to reduced migration and proliferation of smooth muscle cells but not secondarily to a lowering of serum lipid.
引用
收藏
页码:37 / 42
页数:6
相关论文
共 29 条
[1]   WHAT CONTROLS SMOOTH-MUSCLE PHENOTYPE [J].
CHAMLEYCAMPBELL, JH ;
CAMPBELL, GR .
ATHEROSCLEROSIS, 1981, 40 (3-4) :347-357
[2]   PHENOTYPE-DEPENDENT RESPONSE OF CULTURED AORTIC SMOOTH-MUSCLE TO SERUM MITOGENS [J].
CHAMLEYCAMPBELL, JH ;
CAMPBELL, GR ;
ROSS, R .
JOURNAL OF CELL BIOLOGY, 1981, 89 (02) :379-383
[3]   RELATIONSHIP BETWEEN MEVALONATE PATHWAY AND ARTERIAL MYOCYTE PROLIFERATION - IN-VITRO STUDIES WITH INHIBITORS OF HMG-COA REDUCTASE [J].
CORSINI, A ;
MAZZOTTI, M ;
RAITERI, M ;
SOMA, MR ;
GABBIANI, G ;
FUMAGALLI, R ;
PAOLETTI, R .
ATHEROSCLEROSIS, 1993, 101 (01) :117-125
[4]   REQUIREMENT FOR MEVALONATE IN CYCLING CELLS - QUANTITATIVE AND TEMPORAL ASPECTS [J].
DOYLE, JW ;
KANDUTSCH, AA .
JOURNAL OF CELLULAR PHYSIOLOGY, 1988, 137 (01) :133-140
[5]  
FAIRBANKS KP, 1984, J BIOL CHEM, V259, P1546
[6]   HELSINKI HEART-STUDY - PRIMARY-PREVENTION TRIAL WITH GEMFIBROZIL IN MIDDLE-AGED MEN WITH DYSLIPIDEMIA - SAFETY OF TREATMENT, CHANGES IN RISK-FACTORS, AND INCIDENCE OF CORONARY HEART-DISEASE [J].
FRICK, MH ;
ELO, O ;
HAAPA, K ;
HEINONEN, OP ;
HEINSALMI, P ;
HELO, P ;
HUTTUNEN, JK ;
KAITANIEMI, P ;
KOSKINEN, P ;
MANNINEN, V ;
MAENPAA, H ;
MALKONEN, M ;
MANTTARI, M ;
NOROLA, S ;
PASTERNACK, A ;
PIKKARAINEN, J ;
ROMO, M ;
SJOBLOM, T ;
NIKKILA, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (20) :1237-1245
[7]   REGULATION OF THE MEVALONATE PATHWAY [J].
GOLDSTEIN, JL ;
BROWN, MS .
NATURE, 1990, 343 (6257) :425-430
[8]  
HABENICHT AJR, 1980, J BIOL CHEM, V255, P5134
[9]   EFFECT OF FLUVASTATIN SODIUM (XU62-320), A NEW INHIBITOR OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE, ON THE INDUCTION OF LOW-DENSITY-LIPOPROTEIN RECEPTOR IN HEPG2 CELLS [J].
HAYASHI, K ;
KUROKAWA, J ;
NOMURA, S ;
KUGA, Y ;
OHKURA, Y ;
KAJIYAMA, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1167 (02) :223-225
[10]  
HJERMANN I, 1981, LANCET, V2, P1303