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Article detail · 2024

Protective Effect of Astaxanthin on Histopathologic Changes Induced by Bisphenol A in the Liver of Rats

Journal

The Pakistan Veterinary Journal

ISSN 0253-8318

The ISSN points to another catalog journal; the name is from the YÖKSİS record.

YÖKSİS OpenAlex Open access · gold SJR Q1 JCR Q1 Citations 8 Percentile 83.9% FWCI 1.89
Year
2024
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • YÖKSİS venue The Pakistan Veterinary Journal
  • Catalog match (ISSN) Pakistan Veterinary Journal
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

Abstract

English (OpenAlex)

Bisphenol A (BPA) has several potential uses, including in polycarbonate plastics and epoxy resins, which could expose humans to it.Recognized for its hepatotoxicity and ability to accumulate in organs.We prompted this study to explore the hepatoprotective potential of astaxanthin (ASTX), an antioxidant against BPA toxicity.We used 32 male Wistar Albino rats and randomly assigned them as: Control, Sham (olive oil), BPA, and BPA+ASTX.At the end of the experiment, Native Thiol, Total Thiol, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) were measured in serum samples.Histopathological scoring was performed to evaluate the changes caused by ASTX in the liver.Caspase 3 and caspase 9 expression in liver tissues was demonstrated immunohistochemically and by PCR.Collagen I (COL1A1) and collagen III (COL3A1) mRNA levels were measured by PCR in the tissue samples.The BPA group showed elevated AST and ALT with decreased Thiol levels.ASTX administration reversed these changes as observed by reduced AST and ALT levels and increased Thiol levels.Histopathology indicated increased liver damage and fibrosis in the BPA group which were alleviated in the BPA+ASTX group.Gene expression analyses revealed upregulated COL1A1 and COL3A1 in BPA, which was downregulated with ASTX.Immunohistochemistry and PCR confirmed BPA-induced caspase 3 and caspase 9 expression, which were attenuated by ASTX.This study underscores ASTX's hepatoprotective efficacy against BPA-induced hepatotoxicity which ultimately attributed to its antioxidant and antiapoptotic properties.Consequently, ASTX emerges as a promising therapeutic agent for preventing and treating BPA-related liver diseases.

Topics

  • Effects and risks of endocrine disrupting chemicals

Primary topic Effects and risks of endocrine disrupting chemicals

Authors

  1. SEDA ÇETİNKAYA KARABEKİR
  2. BURCU GÜLTEKİN
  3. İLKNUR ÇINAR AYAN
  4. HASAN BAHRİ SAVAŞ
  5. GÖKHAN CÜCE
  6. SABİHA SERPİL KALKAN NECMETTİN ERBAKAN ÜNİVERSİTESİ