Korean J Physiol Pharmacol 2025; 29(2): 245-255
Published online March 1, 2025 https://doi.org/10.4196/kjpp.24.352
Copyright © Korean J Physiol Pharmacol.
Hongliang Li1,2,#,*, Bingqian Ye1,#, Jiping Tian1, Bofan Wang1, Yiwen Zha1, Shuying Zheng1, Tan Ma1,2, Wenwen Zhuang3, Won Sun Park1,*, and Jingyan Liang1,2,*
1Institute of Translational Medicine, Medical College, Yangzhou University, 2Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou University, Yangzhou 225001, Jiangsu, China, 3Department of Physiology, Kangwon National University School of Medicine, Chuncheon 24341, Korea
Correspondence to:Hongliang Li
E-mail: lihongliang0818@yzu.edu.cn
Won Sun Park
E-mail: parkws@kangwon.ac.kr
Jingyan Liang
E-mail: jyliang@yzu.edu.cn
#These authors contributed equally to this work.
Author contributions: H.L. designed the study and revised the manuscript. B.Y. drafted the manuscript and performed all experiments. J.T. and B.W. performed the cell-based assay experiments. Y.Z. and S.Z. analysised the data. T.M. revised the manuscript. W.Z. analysised the data. W.S.P. and J.L. supervised and coordinated the study.
Monotropein is a compound classified into iridoid which is found in herbaceous plants Morindae officinalis. It possesses anti-inflammatory, antioxidant, and anti-osteoarthritic activities. Previous study indicates that monotropein may have the potential to combat cardiovascular disease, although the related mechanism remains unclear. In this study, we constructed the model of atherosclerosis by oxidized low density lipoprotein-induced vascular smooth muscle cells and LDLR–/– mice given high-fat diet to investigate the effects of monotropein on atherosclerosis. Our results showed that monotropein treatment significantly reduced the area of atherosclerotic plaques and necrotic cores in mice, inhibited the proliferation and migration of vascular smooth muscle cells, and reduced inflammatory responses and oxidative stress, which in turn alleviated atherosclerosis. In addition, we found that monotropein reduced the expression levels of P-NF-κB and P-AP-1. In conclusion, our data suggest that monotropein inhibited the proliferation and migration of vascular smooth muscle cells by mediating the activity of NF-κB, AP-1, reducing the level of inflammation and oxidative stress, and thus resisting the development of atherosclerosis. These findings demonstrate the efficacious therapeutic impact of monotropein on atherosclerosis and elucidate its specific target.
Keywords: Atherosclerosis, Migration, Monotropein, Proliferation, Vascular smooth muscle
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