Biochemical and Biophysical Research Communications · 2014 · 15 citations · 16 references
MedicineCardiologyPharmacologyCardiovascular PharmacotherapyClinical PharmacologyMolecular PharmacologyAtherosclerosis PharmacotherapyCardiovascular DiseaseCardiovascular PharmacodynamicsCardiovascular PharmacologyCoronary Artery DiseaseAtherosclerosis Molecular MechanismsAtherosclerosis RiskAtherosclerotic Plaque RuptureCardiovascular Drug PharmacologyNicotine Receptor PharmacologyNicotinic Acetylcholine Receptor AgonismNicotinic AntagonistsNicotinic Receptor Pharmacology
Varenicline is one of the most widely used drugs for smoking cessation. However, whether an adverse effect of varenicline is associated with the risk of serious cardiovascular events remains controversial. In this study, we determined if varenicline increases the risk of cardiovascular events using apolipoprotein E knockout (ApoE KO) mice. ApoE KO mice (8 weeks old) were injected with varenicline 0.5 mg kg(-1)day(-1) for 3 weeks. Varenicline aggravated atherosclerotic plaque formation in whole aorta from ApoE KO mice compared with vehicle. Methyllycaconitine, an α7 nicotinic acetylcholine receptor (nAChR) antagonist, inhibited varenicline-induced aggravated plaque formation. Our findings show that varenicline progresses atherosclerotic plaque formation through α7 nAChR, and thereby increases the risk of cardiovascular events.
16