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Updated: Sep 14, 2026

Calcification of Vascular Smooth Muscle Cells and Imaging of Aortic Calcification and Inflammation
Published on: May 31, 2016
Calcium, calcium antagonists and experimental atherosclerosis
R Paoletti1, A Corsini, M R Soma
1Institute of Pharmacological Sciences, University of Milan, Italy.
Abstract:
Several calcium entry blockers have shown an antiatherosclerotic effect both in vitro and in vivo. The effects are particularly evident against smooth muscle cell migration multiplication, matrix formation, calcium and cholesterol accumulation. Among the new calcium antagonists, isradipine, amlodipine and lacidipine, are promising as antiatherosclerotic agents. Lacidipine is particularly interesting because of its lipophylic structure and accumulation in cell membranes. Lacidipine is structurally related to nifedipine; we observed that lacidipine inhibits three major processes of atherogenesis: cholesteryl ester metabolism in macrophages, proliferation of myocytes, and their migration.
Insights
Calcium channel blockers like lacidipine show antiatherosclerotic effects by inhibiting key processes in artery disease development. These drugs are promising for preventing atherosclerosis progression.
Area of Science:
- Cardiovascular Pharmacology
- Atherosclerosis Research
Background:
- Calcium entry blockers demonstrate antiatherosclerotic properties in vitro and in vivo.
- These effects are notable in reducing smooth muscle cell migration, multiplication, matrix formation, and lipid accumulation.
Purpose of the Study:
- To evaluate the antiatherosclerotic potential of new calcium antagonists, specifically isradipine, amlodipine, and lacidipine.
- To investigate the mechanisms by which lacidipine inhibits atherogenesis.
Main Methods:
- In vitro and in vivo studies were conducted.
- The study focused on the effects of lacidipine on macrophage cholesteryl ester metabolism, myocyte proliferation, and myocyte migration.
Main Results:
- Lacidipine, a lipophilic calcium antagonist, accumulates in cell membranes.
- Lacidipine was observed to inhibit cholesteryl ester metabolism in macrophages.
- Lacidipine effectively inhibited both proliferation and migration of myocytes.
Conclusions:
- Lacidipine exhibits significant antiatherosclerotic activity.
- Its lipophilic nature and ability to inhibit key atherogenic processes make lacidipine a promising therapeutic agent for atherosclerosis.
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