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Angiotensin converting enzyme inhibitors and atherosclerosis
R G Andersson1, L Jacobsson, K Persson
1Department of Pharmacology, Faculty of Health Sciences, Linköping University, Sweden.
Summary
Angiotensin converting enzyme (ACE) inhibitors, captopril and fosinopril, demonstrated antiatherosclerotic effects in hypercholesterolemic mini-pigs. These drugs reduced arterial atherosclerosis and cholesterol accumulation, suggesting a therapeutic benefit.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Atherosclerosis Research
Background:
- Atherosclerosis is a major cause of cardiovascular disease.
- Hypercholesterolemia is a primary risk factor for atherosclerosis development.
- Angiotensin converting enzyme (ACE) inhibitors are widely used to treat hypertension and heart failure.
Purpose of the Study:
- To evaluate the antiatherosclerotic effects of ACE inhibitors.
- To investigate the impact of captopril and fosinopril on atherosclerosis in a mini-pig model.
- To assess the influence of ACE inhibitors on arterial function and lipid profiles.
Main Methods:
- Experimental hypercholesterolemia and atherosclerosis were induced in Göttingen mini-pigs over 52 weeks.
- Animals were treated with captopril (80 mg/kg/day) or fosinopril (8 mg/kg/day) or served as controls.
- Atherosclerotic lesions, arterial cholesterol content, and endothelium-dependent relaxation were analyzed.
Main Results:
- Both captopril and fosinopril significantly reduced visible atherosclerosis in the abdominal aorta.
- Arterial cholesterol accumulation in the thoracic and abdominal aorta was significantly decreased by ACE inhibitors.
- ACE inhibitors modulated serum ACE activity, plasma renin activity, and aldosterone concentration with minor effects on plasma lipids.
Conclusions:
- ACE inhibitors captopril and fosinopril exhibit significant antiatherosclerotic properties.
- These findings suggest a potential therapeutic role for ACE inhibitors in preventing or treating atherosclerosis.
- Further research is warranted to elucidate the mechanisms underlying the observed antiatherosclerotic effects.