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Published on: October 26, 2020
[Prevention of target organ damage with modern antihypertensive agents]
Dénes Páll1, Eva Katona, Mária Juhász
1Orvos- és Egészségtudományi, Centrum, I. Belgyógyászati Klinika, Debrecen.
Insights
Combining amlodipine, a calcium channel blocker, with lisinopril, an ACE inhibitor, effectively lowers blood pressure and reduces cardiovascular risk. This combination therapy offers improved tolerability and compliance for hypertension management.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Epidemiology
Context:
- Hypertension is a complex condition requiring multifaceted treatment approaches.
- Recent epidemiological data highlight the need for effective blood pressure management.
- Target organ damage and accelerated clinical conditions necessitate optimized therapeutic strategies.
Purpose:
- To review current epidemiological data on hypertension.
- To evaluate the efficacy and safety of combined amlodipine and lisinopril therapy.
- To emphasize the benefits of fixed-dose combination therapy in cardiovascular risk reduction.
Summary:
- Amlodipine (a third-generation dihydropyridine calcium channel blocker) exhibits antihypertensive, anti-ischemic, and anti-atherosclerosis properties.
- Lisinopril (a first-line ACE inhibitor) demonstrates benefits in treating left ventricular hypertrophy, retinopathy, nephropathy, and improving outcomes post-myocardial infarction and in heart failure.
- Combined amlodipine-lisinopril therapy shows additive effects, reducing side effects and improving patient compliance, as supported by studies like ASCOT, CAFE, and HAMLET.
Impact:
- Fixed-dose combination of amlodipine-lisinopril provides effective blood pressure reduction.
- This combination therapy significantly reduces cardiovascular risk.
- The amlodipine-lisinopril combination demonstrates good tolerability and favorable patient compliance.
Abstract:
This review summarises the recent epidemiological data on hypertension, the aims of the treatment of hypertension, and emphasizes the importance of the modification of target organ damages and accelerated clinical conditions. Because the pathogenesis of hypertension is extremely complex, the therapy most likely requires a combined drug administration. The modern third generation dihydropyridine calcium channel blocker, amlodipine, not only has a favourable antihypertensive and anti-ischemic effect, but anti-atherosclerosis properties as well. There are plenty of evidence which demonstrate that lisinopril, a first line antihypertensive agent, has a positive effect in the treatment of left ventricular hypertrophy, retinopathy and nephropathy, and also has a favourable outcome after myocardial infarction and in heart failure. The combined administration of the two drugs leads to a favourable additive effect, with a decrease in the number and severity of side effects. The results of the ASCOT study proved a favourable effect with amlodipine based, combination therapy with an ACE-inhibitor, compared with the traditional beta-blockers and diuretics. The data of the CAFE sub-study showed, that in spite of the similar peripheral antihypertensive effect, the amlodipine based therapy decreased the central aortic pulse pressure to a greater extent. The central aortic pressure showed a good correlation with the end-points of the study, respectively. The results of the Hungarian multicenter study (HAMLET) proved the effective and safe administration of the two drugs in combination. Based on the above evidence, the fixed-dose combination of the CCB-ACE inhibitor (amlodipine-lisinopril) has not only effective blood pressure reducing properties, but also results in cardiovascular risk reduction, good tolerability and favourable compliance.
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