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Article

Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells

  • Authors:
    • B. Relja
    • N. Omid
    • N. Wagner
    • K. Mörs
    • I. Werner
    • E. Juengel
    • M. Perl
    • I. Marzi
  • View Affiliations / Copyright

    Affiliations: Department of Trauma, Hand and Reconstructive Surgery, University Hospital Frankfurt, Goethe University Frankfurt am Main, D-60590 Frankfurt, Germany, Department of Thoracic and Cardiovascular Surgery, University Hospital Frankfurt, Goethe University Frankfurt am Main, D-60590 Frankfurt, Germany, Department of Urology and Pediatric Urology, University Hospital Frankfurt, Goethe University Frankfurt am Main, D-60590 Frankfurt, Germany, Department of Trauma Surgery, Trauma Center Murnau, D-82418 Murnau, Germany
  • Pages: 517-525
    |
    Published online on: December 11, 2015
       https://doi.org/10.3892/ijmm.2015.2431
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Abstract

Increases in pro-inflammatory cytokine levels and tissue-infiltrating leukocytes have been closely linked to increased systemic and local inflammation, which result in organ injury. Previously, we demonstrated the beneficial and hepatoprotective anti-inflammatory effects of acute ethanol (EtOH) ingestion in an in vivo model of acute inflammation. Due to its undesirable side-effects, however, EtOH does not represent a therapeutic option for treatment of acute inflammation. Therefore, in this study, we compared the effects of acute EtOH exposure with ethyl pyruvate (EtP) as an alternative anti-inflammatory drug in an in vitro model of hepatic and pulmonary inflammation. Human hepatocellular carcinoma cells Huh7 and alveolar epithelial cells A549 were stimulated with either interleukin (IL) IL-1β (1 ng/ml, 24 h) or tumor necrosis factor (TNF) (10 ng/ml, 4 h), and then treated with EtP (2.5-10 mM), sodium pyruvate (NaP, 10 mM) or EtOH (85-170 mM) for 1 h. IL-6 or IL-8 release from Huh7 or A549 cells, respectively, was measured by an enzyme‑linked immunosorbent assay. Neutrophil adhesion to cell monolayers and CD54 expression were also analyzed. Bcl-2 and Bax gene expression was determined by RT-qPCR, and western blot analysis was performed to determine the mechanisms involved. Treating A549 cells with either EtOH or EtP significantly reduced the IL-1β- or TNF‑induced IL-8 release, whereas treating Huh7 cells did not significantly alter IL-6 release. Similarly, neutrophil adhesion to stimulated A549 cells was significantly reduced by EtOH or EtP, whereas for Huh7 cells the tendency for reduced neutrophil adhesion rates by EtOH or EtP was not significant. CD54 expression was noticeably reduced in A549 cells, but this was not the case in Huh7 cells after treatment. The Bax/Bcl-2 ratio was dose‑dependently decreased by EtOH and by high-dose EtP in A549 cells, indicating a reduction in apoptosis, whereas this effect was not observed in Huh7 cells. The underlying mechanisms involve reduced phosphorylation of Akt and nuclear factor-κB (NF-κB) p65. We noted that as with EtP, EtOH reduced the inflammatory response in lung epithelial cells under acute inflammatory conditions. However, due to the low impact which EtP and EtOH had on the hepatocellular cells, our data suggest that both substances exerted different effects depending on the cellular entity. The possible underlying mechanisms involved the downregulation of Akt and the transcription factor NF-κB, but further research on this subject is required.
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Copy and paste a formatted citation
Spandidos Publications style
Relja B, Omid N, Wagner N, Mörs K, Werner I, Juengel E, Perl M and Marzi I: Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells. Int J Mol Med 37: 517-525, 2016.
APA
Relja, B., Omid, N., Wagner, N., Mörs, K., Werner, I., Juengel, E. ... Marzi, I. (2016). Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells. International Journal of Molecular Medicine, 37, 517-525. https://doi.org/10.3892/ijmm.2015.2431
MLA
Relja, B., Omid, N., Wagner, N., Mörs, K., Werner, I., Juengel, E., Perl, M., Marzi, I."Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells". International Journal of Molecular Medicine 37.2 (2016): 517-525.
Chicago
Relja, B., Omid, N., Wagner, N., Mörs, K., Werner, I., Juengel, E., Perl, M., Marzi, I."Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells". International Journal of Molecular Medicine 37, no. 2 (2016): 517-525. https://doi.org/10.3892/ijmm.2015.2431
Copy and paste a formatted citation
x
Spandidos Publications style
Relja B, Omid N, Wagner N, Mörs K, Werner I, Juengel E, Perl M and Marzi I: Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells. Int J Mol Med 37: 517-525, 2016.
APA
Relja, B., Omid, N., Wagner, N., Mörs, K., Werner, I., Juengel, E. ... Marzi, I. (2016). Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells. International Journal of Molecular Medicine, 37, 517-525. https://doi.org/10.3892/ijmm.2015.2431
MLA
Relja, B., Omid, N., Wagner, N., Mörs, K., Werner, I., Juengel, E., Perl, M., Marzi, I."Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells". International Journal of Molecular Medicine 37.2 (2016): 517-525.
Chicago
Relja, B., Omid, N., Wagner, N., Mörs, K., Werner, I., Juengel, E., Perl, M., Marzi, I."Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells". International Journal of Molecular Medicine 37, no. 2 (2016): 517-525. https://doi.org/10.3892/ijmm.2015.2431
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