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Article

Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats

  • Authors:
    • Yanmin Zhang
    • Yong Yang
  • View Affiliations / Copyright

    Affiliations: Department of Emergency, Liaocheng People's Hospital of Shandong, Liaocheng, Shandong 252000, P.R. China, Department of Cardiology, Liaocheng People's Hospital of Shandong, Liaocheng, Shandong 252000, P.R. China
  • Pages: 4839-4845
    |
    Published online on: January 10, 2018
       https://doi.org/10.3892/mmr.2018.8420
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Abstract

The present study aimed to determine the protective effects of arctigenin against myocardial infarction (MI), and its effects on oxidative stress and inflammation in rats. Left anterior coronary arteries of Sprague‑Dawley rats were ligated, in order to generate an acute MI (AMI) model. Arctigenin was administered to AMI rats at 0, 50, 100 or 200 µmol/kg. Western blotting and ELISAs were performed to analyze protein expression and enzyme activity. Arctigenin was demonstrated to effectively inhibit the levels of alanine transaminase, creatine kinase‑MB and lactate dehydrogenase, and to reduce infarct size in AMI rats. In addition, the activity levels of malondialdehyde, interleukin (IL)‑1β and IL‑6 were significantly suppressed, and the levels of glutathione peroxidase, catalase and superoxide dismutase were significantly increased by arctigenin treatment. Arctigenin treatment also suppressed the protein expression levels of inducible nitric oxide synthase (iNOS), cyclooxygenase 2 (COX‑2) and heme oxygenase 1 (HO‑1), and increased the protein expression levels of phosphorylated‑extracellular signal‑regulated kinase 1/2 (p‑ERK1/2) in AMI rats. Overall, the results of the present study suggest that arctigenin may inhibit MI, and exhibits antioxidative and anti‑inflammatory effects through regulation of the iNOS, COX‑2, ERK1/2 and HO‑1 pathways in a rat model of AMI.
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Copy and paste a formatted citation
Spandidos Publications style
Zhang Y and Yang Y: Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats. Mol Med Rep 17: 4839-4845, 2018.
APA
Zhang, Y., & Yang, Y. (2018). Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats. Molecular Medicine Reports, 17, 4839-4845. https://doi.org/10.3892/mmr.2018.8420
MLA
Zhang, Y., Yang, Y."Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats". Molecular Medicine Reports 17.3 (2018): 4839-4845.
Chicago
Zhang, Y., Yang, Y."Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats". Molecular Medicine Reports 17, no. 3 (2018): 4839-4845. https://doi.org/10.3892/mmr.2018.8420
Copy and paste a formatted citation
x
Spandidos Publications style
Zhang Y and Yang Y: Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats. Mol Med Rep 17: 4839-4845, 2018.
APA
Zhang, Y., & Yang, Y. (2018). Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats. Molecular Medicine Reports, 17, 4839-4845. https://doi.org/10.3892/mmr.2018.8420
MLA
Zhang, Y., Yang, Y."Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats". Molecular Medicine Reports 17.3 (2018): 4839-4845.
Chicago
Zhang, Y., Yang, Y."Arctigenin exerts protective effects against myocardial infarction via regulation of iNOS, COX‑2, ERK1/2 and HO‑1 in rats". Molecular Medicine Reports 17, no. 3 (2018): 4839-4845. https://doi.org/10.3892/mmr.2018.8420
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