Turmeric Extract-loaded Selenium Nanoparticles Counter Doxorubicin-induced Hepatotoxicity in Mice via Repressing Oxidative Stress, Inflammatory Cytokines, and Cell Apoptosis.

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      Publisher: Bentham Science Publishers Country of Publication: Netherlands NLM ID: 101265649 Publication Model: Print Cited Medium: Internet ISSN: 1875-5992 (Electronic) Linking ISSN: 18715206 NLM ISO Abbreviation: Anticancer Agents Med Chem Subsets: MEDLINE
    • Publication Information:
      Publication: Amsterdam : Bentham Science Publishers
      Original Publication: Sharjah, U.A.E. ; San Francisco, CA : Bentham Science Publishers, [2006]-
    • Subject Terms:
    • Abstract:
      Background: Doxorubicin (DOX) is an antitumor anthracycline used to treat a variety of malignancies; however, its clinical use is associated with noticeable hepatotoxicity. Therefore, the current study was designed to delineate if biosynthesized SeNPs with turmeric extract (Tur-SeNPs) could alleviate DOX-induced hepatic adverse effects.
      Methods: Mice were orally post-treated with Tur extract, Tur-SeNPs, or N-acetyl cysteine after the intraperitoneal injection of DOX.
      Results: Our findings have unveiled a remarkable liver attenuating effect in DOX-injected mice post-treated with Tur-SeNPs. High serum levels of ALT, AST, ALP, and total bilirubin induced by DOX were significantly decreased by Tur-SeNPs therapy. Furthermore, Tur-SeNPs counteracted DOX-caused hepatic oxidative stress, indicated by decreased MDA and NO levels along with elevated levels of SOD, CAT, GPx, GR, GSH, and mRNA expression levels of Nrf-2. Noteworthily, decreased hepatic IL-1β, TNF-α, and NF-κB p65 levels in addition to downregulated iNOS gene expression in Tur-SeNPs-treated mice have indicated their potent antiinflammatory impact. Post-treatment with Tur-SeNPs also mitigated the hepatic apoptosis evoked by DOX injection. A liver histological examination confirmed the biochemical and molecular findings.
      Conclusions: In brief, the outcomes have demonstrated Tur loaded with nanoselenium to successfully mitigate the liver damage induced by DOX via blocking oxidative stress, and inflammatory and apoptotic signaling.
      (Copyright© Bentham Science Publishers; For any queries, please email at [email protected].)
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    • Grant Information:
      DSR-2021-03-03112 Deanship of Scientific Research at Jouf University
    • Contributed Indexing:
      Keywords: Nanoselenium; apoptosis; doxorubicin; hepatotoxicity; oxidative stress.; turmeric extract
    • Accession Number:
      80168379AG (Doxorubicin)
      H6241UJ22B (Selenium)
      0 (Plant Extracts)
      0 (Cytokines)
      856YO1Z64F (turmeric extract)
      0 (Antibiotics, Antineoplastic)
    • Publication Date:
      Date Created: 20240111 Date Completed: 20240528 Latest Revision: 20240528
    • Publication Date:
      20240528
    • Accession Number:
      10.2174/0118715206274530231213104519
    • Accession Number:
      38204261