Pravastatin and Sarpogrelate Synergistically Ameliorate Atherosclerosis in LDLr-Knockout Mice

PLoS One. 2016 Mar 7;11(3):e0150791. doi: 10.1371/journal.pone.0150791. eCollection 2016.

Abstract

Pravastatin is a lipid-lowering agent that attenuates atherosclerosis. However, the multifactorial pathogenesis of atherosclerosis requires other drugs with different anti-atherogenic mechanisms. We chose sarpogrelate as an anti-platelet agent and a novel component of a complex drug with pravastatin due to its high potential but little information on its beneficial effects on atherosclerosis. Low-density lipoprotein receptor-knockout mice were fed a high-fat, high-cholesterol diet and treated with pravastatin alone, sarpogrelate alone, or a combination of both drugs. Although sarpogrelate alone did not significantly reduce atherosclerotic plaque areas, co-treatment with pravastatin significantly decreased aortic lesions compared to those of the pravastatin alone treated group. The combined therapy was markedly more effective than that of the single therapies in terms of foam cell formation, smooth muscle cell proliferation, and inflammatory cytokine levels. These results suggest that pravastatin and sarpogrelate combined therapy may provide a new therapeutic strategy for treating atherosclerosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atherosclerosis / blood
  • Atherosclerosis / drug therapy*
  • Atherosclerosis / genetics*
  • Atherosclerosis / immunology
  • Cell Proliferation / drug effects
  • Cytokines / metabolism
  • Drug Synergism
  • Gene Expression Regulation / drug effects
  • Gene Knockout Techniques*
  • Hypolipidemic Agents / pharmacology
  • Hypolipidemic Agents / therapeutic use
  • Intercellular Adhesion Molecule-1 / metabolism
  • Lipids / blood
  • Macrophages / drug effects
  • Macrophages / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Monocytes / drug effects
  • Monocytes / immunology
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / pathology
  • Plaque, Atherosclerotic / prevention & control
  • Pravastatin / pharmacology*
  • Pravastatin / therapeutic use
  • Receptors, LDL / deficiency*
  • Receptors, LDL / genetics*
  • Succinates / pharmacology*
  • Succinates / therapeutic use

Substances

  • Cytokines
  • Hypolipidemic Agents
  • Lipids
  • Receptors, LDL
  • Succinates
  • Intercellular Adhesion Molecule-1
  • sarpogrelate
  • Pravastatin

Grants and funding

This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education [2013R1A1A2009176]; the Bio & Medical Technology Development Program of the NRF funded by the Ministry of Science, ICT, & Future Planning [NRF-2013M3A9B5075839]; and Research Fund 2016 of the Catholic University of Korea.