4.0 Article

Extract of Curcuma zedoaria R. prevents atherosclerosis in apolipoprotein E-deficient mice

Journal

NUTRITION RESEARCH AND PRACTICE
Volume 15, Issue 3, Pages 319-328

Publisher

KOREAN NUTRITION SOC
DOI: 10.4162/nrp.2021.15.3.319

Keywords

Curcuma zedoaria; atherosclerosis; ApoE knockout mice; VCAM-1; chemokine CX3CL1

Funding

  1. Korea Institute of Oriental Medicine (KIOM) [KSN2012330]
  2. Soonchunhyang University Research Fund

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The study showed that dietary intake of Curcuma zedoaria extract reduced atherosclerosis in mice, along with decreasing serum triglyceride and high-density lipoprotein levels, and reducing inflammatory molecule expression.
BACKGROUND/OBJECTIVES: Curcuma zedoaria R. (Zingiberaceae) has been used to treat headache, fever, and hypertension-related symptoms in Asian countries, including Korea, China, and Japan. We investigated whether dietary intake of a C. zedoaria extract (CzE) affected atherosclerosis in vivo. MATERIALS/METHODS: Apolipoprotein E-deficient (ApoE(-/-)) mice (n = 32) were fed a normal diet (ND), a high-cholesterol diet (HCD), an HCD containing CzE (100 mg/kg/day), or an HCD containing simvastatin (10 mg/kg/day) for 12 weeks. The anti-atherosclerotic effects were evaluated by observing changes in fatty streak lesions, immunohistochemical analysis, ex vivo fluorescence imaging, lipid profiles, and western blot analysis. RESULTS: The CzE-fed group showed a 41.6% reduction of atherosclerosis. Furthermore, CzE significantly reduced the levels of serum triglyceride, high-density lipoprotein, the chemokine (C-X3-C-motif) ligand 1, the adhesion molecules vascular cell adhesion molecule-1, intracellular adhesion molecule-1, and E-selectin; down-regulation of tumor necrosis factor-alpha, interleukin-6, high mobility group box-1, and cathepsin levels in the aortic sinuses and aortas of ApoE(-/-) mice were also observed. CONCLUSIONS: The results suggest that the inclusion of a water extract of C. zedoaria in a HCD is closely correlated with reducing the risk of vascular inflammatory diseases in an ApoE mouse model.

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