EFFECTS OF ETIDRONATE AND LOVASTATIN ON THE REGRESSION OF ATHEROSCLEROSIS IN CHOLESTEROL-FED RABBITS

被引:21
作者
ZHU, BQ
SUN, YP
SIEVERS, RE
ISENBERG, WM
MOOREHEAD, TJ
PARMLEY, WW
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT MED,DIV CARDIOVASC,SAN FRANCISCO,CA
[2] UNIV CALIF SAN FRANCISCO,CARDIOVASC RES INST,SAN FRANCISCO,CA
[3] PROCTOR & GAMBLE PHARMACEUT,NORWICH,NY
关键词
ETIDRONATE; LOVASTATIN; ATHEROSCLEROSIS; PLAQUE THICKNESS; CHOLESTEROL-FED RABBIT;
D O I
10.1159/000176738
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Eighty New Zealand rabbits in eight groups (10 each) were fed a 0.5% cholesterol diet for 12 weeks. One group served as a control and was sacrificed at the end of 12 weeks. Seven other groups were shifted to a normal diet and received a drug(s) or placebo for the second 12 weeks. The high dose of etidronate (3 mg/kg/day) with lovastatin (6 mg/kg/day) significantly reduced the percent of aortic atherosclerotic lesions [56 +/- 21 vs. 77 +/- 17% (mean +/- SD), p < 0.05] in the regression study. Compared to the control groups for etidronate and lovastatin, the high or low dose (0.15 mg/kg/day) of etidronate significantly reduced aortic standardized plaque volume per unit (18.7 +/- 7.9 or 18.8 +/- 9.1 vs. 28.4 +/- 11.8 mm.%, p < 0.05). Lovastatin reduced pulmonary artery maximum plaque thickness (0.13 +/- 0.10 vs. 0.23 +/- 0.11 mm, p < 0.05). There were no differences in serum lipid and calcium levels in the control and treated groups. The high dose of etidronate inhibited bone mineralization as expected, whereas the low dose of etidronate did not. These data suggest that etidronate with lovastatin can regress aortic atherosclerosis in the cholesterol-fed rabbit placed on a normal diet.
引用
收藏
页码:370 / 377
页数:8
相关论文
共 15 条
[1]   INFLUENCE OF DISODIUM ETIDRONATE ON CLINICAL AND LABORATORY MANIFESTATIONS OF PAGETS-DISEASE OF BONE (OSTEITIS DEFORMANS) [J].
ALTMAN, RD ;
JOHNSTON, CC ;
KHAIRI, MRA ;
WELLMAN, H ;
SERAFINI, AN ;
SANKEY, RR .
NEW ENGLAND JOURNAL OF MEDICINE, 1973, 289 (26) :1379-1384
[2]  
AMIN D, 1992, J LIPID RES, V33, P1657
[3]   LIPID-LOWERING AND PLAQUE REGRESSION - NEW INSIGHTS INTO PREVENTION OF PLAQUE DISRUPTION AND CLINICAL EVENTS IN CORONARY-DISEASE [J].
BROWN, BG ;
ZHAO, XQ ;
SACCO, DE ;
ALBERS, JJ .
CIRCULATION, 1993, 87 (06) :1781-1791
[4]   EFFECT OF LOVASTATIN ON INTIMAL HYPERPLASIA AFTER BALLOON ANGIOPLASTY - A STUDY IN AN ATHEROSCLEROTIC HYPERCHOLESTEROLEMIC RABBIT [J].
GELLMAN, J ;
EZEKOWITZ, MD ;
SAREMBOCK, IJ ;
AZRIN, MA ;
NOCHOMOWITZ, LE ;
LERNER, E ;
HAUDENSCHILD, CC .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1991, 17 (01) :251-259
[5]  
GREIF F, 1990, ISRAEL J MED SCI, V26, P301
[6]  
KINGMA JG, 1990, J EXP PATHOL, V71, P145
[7]  
RINGENBERG QS, 1987, CLIN THER, V9, P318
[8]   EFFECT OF DISODIUM ETHANE-1-HYDROXY-1,1-DIPHOSPHONATE (EHDP) ON A RABBIT MODEL OF ATHERO-ARTERIOSCLEROSIS [J].
ROSENBLUM, IY ;
FLORA, L ;
EISENSTEIN, R .
ATHEROSCLEROSIS, 1975, 22 (03) :411-424
[9]  
SCHAIFF RAB, 1989, CLIN PHARMACY, V8, P108
[10]  
SHEVRIN DH, 1985, CLIN PHARMACY, V4, P204