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Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats
[Stratégie et management de l’innovation collaborative : exploration du contexte européen]

Author

Listed:
  • Soufiane Kherrazi

    (EDHEC - EDHEC Business School - UCL - Université catholique de Lille)

  • Karim Said

    (LAREQUOI - Laboratoire de recherche en Management - UVSQ - Université de Versailles Saint-Quentin-en-Yvelines)

Abstract

Hepatitis is one of earlier, but serious, signs of liver damage. High doses of statins for a long time can induce hepatitis. This study aimed to evaluate and compare the therapeutic potential of thymoquinone ( TQ) and bee pollen (BP) on fluvastatin (F)-induced hepatitis in rats. Rats were randomly divided into: group 1 (G1, control), G2 (F, hepatitis), G3 (F + TQ), G4 (F + BP), and G5 (F + TQ + BP). Single treatment with TQ or BP relieved fluvastatin-induced hepatitis, with best effect for the combined therapy. TQ and/or BP treatment significantly (1) reduced serum levels of alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma glutamyl transpeptidase, and total bilirubin, (2) decreased malondialdehyde levels and increased level of reduced glutathione, and activities of glutathione peroxidase and catalase in the liver, (3) improved liver histology with mild deposition of type I collagen, (4) increased mRNA levels of transforming growth factor beta 1, nuclear factor Kappa B, and cyclooxygenase 1 and 2, and (5) decreased tumor necrosis factor alpha and upregulated interleukin 10 protein in the liver. These data clearly highlight the ability of TQ and BP combined therapy to cause better ameliorative effects on fluvastatin-induced hepatitis than individual treatment by each alone.

Suggested Citation

  • Soufiane Kherrazi & Karim Said, 2020. "Potential therapeutic effect of thymoquinone and/or bee pollen on fluvastatin-induced hepatitis in rats [Stratégie et management de l’innovation collaborative : exploration du contexte européen]," Post-Print hal-04397156, HAL.
  • Handle: RePEc:hal:journl:hal-04397156
    DOI: 10.3917/inno.062.0017
    as

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