Anti-malarial Drugs Reduce Vascular Smooth Muscle Cell Proliferation via Activation of AMPK and Inhibition of Smad3 Signaling
10.12997/jla.2019.8.2.267
- Author:
Heejung LEE
1
;
Jung Hwa HAN
;
Sujin KIM
;
Suji KIM
;
Du Hyong CHO
;
Chang Hoon WOO
Author Information
1. Department of Pharmacology and Smart-Ageing Convergence Research Center, Yeungnam University College of Medicine, Daegu, Korea. changhoon_woo@yu.ac.kr
- Publication Type:Original Article
- Keywords:
Chloroquine;
Hydroxychloroquine;
Vascular smooth muscle;
AMP-activated protein kinase;
Intima formation
- MeSH:
Adenosine;
AMP-Activated Protein Kinases;
Animals;
Antimalarials;
Arteries;
Atherosclerosis;
Blotting, Western;
Carotid Arteries;
Cell Count;
Cell Cycle;
Cell Proliferation;
Chloroquine;
Flow Cytometry;
Hydroxychloroquine;
In Vitro Techniques;
Mice;
Microscopy;
Microscopy, Fluorescence;
Muscle, Smooth, Vascular;
Neointima;
Phosphorylation;
Protein Kinases;
Rats;
RNA, Messenger
- From:Journal of Lipid and Atherosclerosis
2019;8(2):267-276
- CountryRepublic of Korea
- Language:English
-
Abstract:
OBJECTIVE: The aim of this study was to investigate the effects of 2 anti-malarial drugs, chloroquine (CQ) and hydroxychloroquine (HCQ), on inhibition of vascular smooth muscle cell (VSMC) proliferation both in vivo and in vitro via Adenosine monophosphate-activated protein kinase (AMPK) activation. METHODS: Protein and mRNA levels were determined by western blot analysis and real-time reverse transcription-polymerase chain reaction in primary rat VSMCs treated with CQ and HCQ, respectively. Cell proliferation was measured by flow cytometry and cell counting. Mice carotid arteries were ligated and treated with CQ or HCQ every other day for 3 weeks. Pathological changes of carotid arteries were visualized by both microscopy and fluorescence microscopy. RESULTS: CQ and HCQ increase AMPK phosphorylation in VSMCs. Both CQ and HCQ decrease platelet-derived growth factor-induced VSMC proliferation and cell cycle progression in an AMPK-dependent manner. In addition, CQ and HCQ inhibit Smad3 phosphorylation and VSMC proliferation induced by transforming growth factor-β1. Moreover, CQ and HCQ diminished neointimal proliferation in a mouse model of carotid artery ligation-induced neointima formation. CONCLUSION: The results demonstrated that CQ and HCQ inhibit cell proliferation and cell cycle progression in VSMCs via the AMPK-dependent signaling pathway. Carotid artery ligation-induced intima thickness was reduced in mouse arteries treated with CQ or HCQ, suggesting a role for antimalarial drugs in treating atherosclerosis and restenosis.
