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
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
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.