Melatonin protects against methotrexate hepatotoxicity in young rats: Impact of PI3K/Akt/mTOR signaling

  • Su Chen Wang
  • , Yi Chuan Huang
  • , Chih Cheng Hsiao
  • , Jiunn Ming Sheen
  • , Li Tung Huang
  • , Wan Shan Lo
  • , Hsin Yi Hsieh
  • , Yu Chieh Chen*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

6 Scopus citations

Abstract

With the improvement in children's acute lymphoblastic leukemia (ALL) care, the survival rate in children ALL has improved much. Methotrexate (MTX) plays an essential role in the success of children's ALL treatment. Since hepatotoxicity is commonly reported in individuals treated with intravenous or oral MTX, our study further examined the hepatic effect following intrathecal MTX treatment, which is an essential treatment for leukemia patients. Specifically, we examined the pathogenesis of MTX hepatotoxicity in young rats and explored the impact of melatonin treatment in protection against MTX hepatotoxicity. Successfully, we found that melatonin was able to protect against MTX hepatotoxicity.

Original languageEnglish
Article numbere23323
Pages (from-to)e23323
JournalJournal of Biochemical and Molecular Toxicology
Volume37
Issue number5
DOIs
StatePublished - 05 2023

Bibliographical note

© 2023 Wiley Periodicals LLC.

Keywords

  • PI3K/Akt/mTOR
  • hepatotoxicity
  • melatonin
  • methotrexate
  • Rats
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • Phosphatidylinositol 3-Kinases
  • Methotrexate/toxicity
  • Proto-Oncogene Proteins c-akt
  • Chemical and Drug Induced Liver Injury/etiology
  • Animals
  • TOR Serine-Threonine Kinases
  • Melatonin/pharmacology

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