Echinochrome guarding effect against sodium arsenite-induced hepatorenal toxicity in rats

  • Hader I. Sakr
  • , Tarek Atia
  • , Neamat A. Mahmoud
  • , Islam Ahmed Abdelmawgood
  • , Marina Lotfy Khalaf
  • , Bassam Waleed Ebeed
  • , Ahmed Mohamed Abdelmohsen
  • , Mohamed A. Kotb
  • , Abdeljalil Mohamed Al Shawoush
  • , Ahmed A. Damanhory
  • , Abdallah Mohammed Elagali
  • , Ayman Saber Mohamed
  • , Hadeer Hesham Abdelfattah

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Background: The persistent and accumulative qualities of the poisonous metalloid arsenic make it a ubiquitous environmental threat. Echinochrome (Ech) is a natural product that possesses antioxidative, antiviral, antialgal, anti-allergic, and antibacterial effects. Aim: The work investigates the beneficial impact of Ech on sodium arsenite-induced hepatorenal toxicity in rats. Eighteen male rats dispersed equally among three groups: control, sodium arsenite (AS), and AS + Ech. Rats were administered AS (10 mg/kg) and Ech (1 mg/kg BW) by gavage for the experimental duration of 30 days. Ech inhibits oxidative stress by improving antioxidant levels, including glutathione, catalase, and glutathione-S-transferase, with a concomitant decrease in the amounts of malondialdehyde and nitric oxide in kidney and liver tissues. Moreover, it reduced blood concentrations of aspartate aminotransferase, alanine aminotransferase, gamma-glutamyltransferase, alkaline phosphatase, serum urea, uric acid, and creatinine. Concurrently, Ech resulted in a substantial increase in albumin and total protein levels. Additionally, Ech inhibits inflammation by reducing serum concentrations of tumor necrosis factor-α, cyclooxygenase 2, and prostaglandin E2. Conclusion: Ech mitigates arsenic-induced hepatorenal damage by inhibiting oxidative stress and inflammatory pathways.

Original languageEnglish
Article number127682
JournalJournal of Trace Elements in Medicine and Biology
Volume90
DOIs
StatePublished - Aug 2025

Keywords

  • Echinochrome
  • Hepatotoxicity
  • Inflammation
  • Nephrotoxicity
  • Oxidative stress
  • Sodium arsenite

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