INHIBITORS OF ANGIOTENSIN-CONVERTING ENZYME DECREASE EARLY ATHEROSCLEROSIS IN HYPERLIPIDEMIC HAMSTERS - FOSINOPRIL REDUCES PLASMA-CHOLESTEROL AND CAPTOPRIL INHIBITS MACROPHAGE FOAM CELL ACCUMULATION INDEPENDENTLY OF BLOOD-PRESSURE AND PLASMA-LIPIDS

Citation
Mc. Kowala et al., INHIBITORS OF ANGIOTENSIN-CONVERTING ENZYME DECREASE EARLY ATHEROSCLEROSIS IN HYPERLIPIDEMIC HAMSTERS - FOSINOPRIL REDUCES PLASMA-CHOLESTEROL AND CAPTOPRIL INHIBITS MACROPHAGE FOAM CELL ACCUMULATION INDEPENDENTLY OF BLOOD-PRESSURE AND PLASMA-LIPIDS, Atherosclerosis, 108(1), 1994, pp. 61-72
Citations number
62
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
00219150
Volume
108
Issue
1
Year of publication
1994
Pages
61 - 72
Database
ISI
SICI code
0021-9150(1994)108:1<61:IOAEDE>2.0.ZU;2-E
Abstract
The effect of two angiotensin converting enzyme (ACE) inhibitors on th e development of atherosclerosis was determined in hyperlipidemic hams ters. Preliminary studies indicated that only fosinopril (50 mg/kg) te mporarily decreased mean arterial pressure, while after chronic dosing fosinopril and captopril (50 mg/kg) were ineffective. The same dose o f fosinopril and captopril inhibited the angiotensin I presser respons e, indicating these agents suppressed ACE activity in vivo. In the 3 w eek atherosclerosis experiment, all hamsters were fed chow supplemente d with 0.05% cholesterol and 10% coconut oil. Control hamsters were co mpared with those receiving either 50 mg/kg per day of fosinopril or 5 0 mg/kg per day of captopril. After 3 weeks, fosinopril reduced plasma total cholesterol, low density lipoprotein (LDL) plus very low densit y lipoprotein cholesterol and total triglycerides by 17%, 27% and 45%, respec tively. Captopril only reduced high density lipoprotein choles terol by 20%. Neither fosinopril or captopril altered blood pressure a t 3 weeks. Atherosclerosis was quantified from en face preparations of the lesion-prone aortic arch that were stained with oil red O (for ch olesteryl ester and triglycerides). In control hamsters, oil red O lab eled numerous subendothelial macrophage-foam cells located along the i nner curvature of the aortic arch. Compared with controls, fosinopril reduced the number of intimal macrophage-foam cells/mm(2), foam cell s ize and the fatty streak area by 85%, 38% and 90%, respectively. Capto pril decreased these parameters by 44%, 16% and 53%. Thus captopril de creased early atherosclerosis without affecting plasma LDL cholesterol or blood pressure, which suggested that inhibiting ACE (or kininase I I) directly impeded the accumulation and formation of macrophage-foam cells. Fosinopril probably further suppressed early atherosclerosis by lowering plasma LDL cholesterol.