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Hydrochlorothiazide abolishes the anti-atherosclerotic effect of quinapril
F A H Fonseca1, S S M Ihara, M C O Izar
1Division of Cardiology, Department of Medicine, Federal University of São Paulo, São Paulo, Brazil. lipides.dmed@unifesp.epm.br
Insights
Diuretics like hydrochlorothiazide did not affect atherosclerosis in rabbits. Quinapril improved blood vessel function and reduced atherosclerosis, but this benefit was diminished when combined with hydrochlorothiazide.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Atherosclerosis Studies
Background:
- Antihypertensive treatments reduce stroke risk but incompletely address coronary risk.
- Hypertension's impact on atherosclerosis warrants further investigation, particularly regarding diuretic effects.
Purpose of the Study:
- To investigate the effects of hydrochlorothiazide and quinapril, alone and in combination, on atherosclerosis.
- To determine if diuretics like hydrochlorothiazide exacerbate or mitigate atherosclerosis progression.
Main Methods:
- New Zealand rabbits were fed a cholesterol-enriched diet to induce atherosclerosis.
- Animals received control, hydrochlorothiazide, quinapril, or combination therapy during the latter 12 weeks.
- Aortic rings were analyzed for endothelium-dependent vasorelaxation and atherosclerotic plaque characteristics.
Main Results:
- Quinapril significantly improved endothelium-dependent vasorelaxation and reduced atherosclerosis markers (intima area, intima/media ratio, plaque presence).
- Hydrochlorothiazide alone did not alter atherosclerosis or vasorelaxation.
- Combination therapy with hydrochlorothiazide blunted the anti-atherosclerotic effects of quinapril.
Conclusions:
- Hydrochlorothiazide does not modify atherosclerosis in this model.
- Quinapril exhibits anti-atherosclerotic properties by improving vasorelaxation and reducing plaque burden.
- Combining hydrochlorothiazide with quinapril diminishes quinapril's beneficial anti-atherosclerotic effects.
Abstract:
1. Antihypertensive treatment has been demonstrated to result in persistent reductions in morbidity and mortality due to stroke. However, the coronary risk attributable to hypertension has been only partially reversed. We hypothesized that diuretics could have unfavourable effects on atherosclerosis. 2. New Zealand rabbits were fed a 0.5% cholesterol-enriched diet for 12 weeks, followed by a 0.1% cholesterol diet for another 12 weeks. During the last 12 week period, 40 animals were randomly assigned to one of four groups: (i) group I was the control group; (ii) group II received hydrochlorothiazide (10 mg/day); (iii) group III received quinapril (30 mg/day); and (iv) group IV was treated with hydrochlorothiazide (10 mg/day) plus quinapril (30 mg/day). 3. The treatments did not affect either the lipid profile or serum electrolytes and oxidative stress. However, endothelium-dependent vasorelaxation in isolated aortic rings was significantly improved with quinapril (group III) treatment (P < 0.001 vs other groups). In addition, therapy with quinapril promoted a significant reduction in atherosclerosis (intima area, intima/media ratio and perimeter of vessel with plaque; P < 0.05 vs other groups), as well as in cholesterol content of the aorta (P < 0.05 vs groups II and IV). 4. In conclusion, hydrochlorothiazide did not modify atherosclerosis and, when added to quinapril treatment, impaired the anti-atherosclerotic effect seen with quinapril alone.
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