Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Wan, Qianga; b; * | Liu, Zhong-yonga | Yang, Yu-pinga | Liu, Shi-mingb
Affiliations: [a] Department of Medical Cardiology, Affiliated Hospital, Jiangxi University of Traditional Chinese Medicine, Nanchang, China | [b] Institute of Cardiovascular Disease, Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China
Correspondence: [*] Corresponding author: Qiang Wan. E-mail: [email protected].
Abstract: Background:Curcumin possesses significant anti-atherosclerosis properties. Lipocalin-2 (LCN2) is already known as one of the most promising biomarkers of atherosclerosis. However, research on the effect of curcumin on regulating LCN2 expression in atherogenesis is very limited. The aim of the study was to investigate whether curcumin could alleviate atherosclerosis in ApoE−/− mice by down-regulating LCN2 expression. Methods:Fifty apolipoprotein E knockout (ApoE−/−) mice were fed with a western diet for 12 weeks and randomly divided into five groups: model group (Mod), positive control group (Lov, with 30 mg/kg/d lovastatin), three curcumin groups (CurL, CurM and CurH, with 40, 60 and 80 mg/kg/d curcumin), while 10 C57BL/6J mice were fed with a standard mouse chow diet as a control group (Con). LCN2 in serum and aorta, biomarkers of serum lipid and inflammation were determined and the plaque area of the atherosclerosis lesions was quantified. Results:CurM and CurH group were significantly lower than Mod group in terms of serum LCN2, lipid and inflammatory cytokine levels, plaque area and LCN2 expression in atherosclerotic lesions, similar to lovastatin treatment. Conclusions:Our findings indicate that dietary curcumin ameliorates western diet-induced atherosclerosis in ApoE−/− mice, which is related to LCN2 down-regulation, anti-hyperlipidemia effect as well as the inhibition of inflammation.
Keywords: Curcumin, atherosclerosis, lipocalin-2 (LCN2), inflammation, anti-hyperlipidemia, apolipoprotein E knockout (ApoE−/−) mice
DOI: 10.3233/BME-161610
Journal: Bio-Medical Materials and Engineering, vol. 27, no. 6, pp. 577-587, 2016
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]