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Article

Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma

  • Authors:
    • Zhen‑Hua Ni
    • Ji‑Hong Tang
    • Guo Chen
    • Yi‑Min Lai
    • Qing‑Ge Chen
    • Zao Li
    • Wei Yang
    • Xu‑Min Luo
    • Xiong‑Biao Wang
  • View Affiliations / Copyright

    Affiliations: Central Laboratory, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200062, P.R. China, Department of Respiratory Medicine, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200062, P.R. China
  • Pages: 287-294
    |
    Published online on: November 6, 2015
       https://doi.org/10.3892/mmr.2015.4520
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Abstract

Previous in vitro studies have demonstrated that resveratrol is able to significantly inhibit the upregulation of mucin 5AC (MUC5AC), a major component of mucus; thus indicating that resveratrol may have potential in regulating mucus overproduction. However, there have been few studies regarding the resveratrol‑mediated prevention of MUC5AC overproduction in vivo, and the mechanisms by which resveratrol regulates MUC5AC expression have yet to be elucidated. In the present study, an ovalbumin (OVA)‑challenged murine model of asthma was used to assess the effects of resveratrol treatment on mucus production in vivo. The results demonstrated that resveratrol significantly inhibited OVA‑induced airway inflammation and mucus production. In addition, the mRNA and protein expression levels of MUC5AC were increased in the OVA‑challenged mice, whereas treatment with resveratrol significantly inhibited this effect. The expression levels of murine calcium‑activated chloride channel (mCLCA)3, an important key mediator of MUC5AC production, were also reduced following resveratrol treatment. Furthermore, in vitro studies demonstrated that resveratrol significantly inhibited human (h)CLCA1 and MUC5AC expression in a dose‑dependent manner. These results indicated that resveratrol was effective in preventing mucus overproduction and MUC5AC expression in vivo, and its underlying mechanism may be associated with regulation of the mCLCA3/hCLCA1 signaling pathway.
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Copy and paste a formatted citation
Spandidos Publications style
Ni ZH, Tang JH, Chen G, Lai YM, Chen QG, Li Z, Yang W, Luo XM and Wang XB: Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma. Mol Med Rep 13: 287-294, 2016.
APA
Ni, Z., Tang, J., Chen, G., Lai, Y., Chen, Q., Li, Z. ... Wang, X. (2016). Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma. Molecular Medicine Reports, 13, 287-294. https://doi.org/10.3892/mmr.2015.4520
MLA
Ni, Z., Tang, J., Chen, G., Lai, Y., Chen, Q., Li, Z., Yang, W., Luo, X., Wang, X."Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma". Molecular Medicine Reports 13.1 (2016): 287-294.
Chicago
Ni, Z., Tang, J., Chen, G., Lai, Y., Chen, Q., Li, Z., Yang, W., Luo, X., Wang, X."Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma". Molecular Medicine Reports 13, no. 1 (2016): 287-294. https://doi.org/10.3892/mmr.2015.4520
Copy and paste a formatted citation
x
Spandidos Publications style
Ni ZH, Tang JH, Chen G, Lai YM, Chen QG, Li Z, Yang W, Luo XM and Wang XB: Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma. Mol Med Rep 13: 287-294, 2016.
APA
Ni, Z., Tang, J., Chen, G., Lai, Y., Chen, Q., Li, Z. ... Wang, X. (2016). Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma. Molecular Medicine Reports, 13, 287-294. https://doi.org/10.3892/mmr.2015.4520
MLA
Ni, Z., Tang, J., Chen, G., Lai, Y., Chen, Q., Li, Z., Yang, W., Luo, X., Wang, X."Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma". Molecular Medicine Reports 13.1 (2016): 287-294.
Chicago
Ni, Z., Tang, J., Chen, G., Lai, Y., Chen, Q., Li, Z., Yang, W., Luo, X., Wang, X."Resveratrol inhibits mucus overproduction and MUC5AC expression in a murine model of asthma". Molecular Medicine Reports 13, no. 1 (2016): 287-294. https://doi.org/10.3892/mmr.2015.4520
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