Ellagic acid ameliorates cisplatin induced hepatotoxicity in colon carcinogenesis.


Journal

Environmental toxicology
ISSN: 1522-7278
Titre abrégé: Environ Toxicol
Pays: United States
ID NLM: 100885357

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 17 09 2018
revised: 07 03 2019
accepted: 14 03 2019
pubmed: 7 4 2019
medline: 3 8 2019
entrez: 7 4 2019
Statut: ppublish

Résumé

The clinical application of cisplatin (CP), one of the most extensively used antineoplastic drug, is restricted by its numerous side effects. CP's antitumor potential resides in the free generation of reactive oxygen species leading to oxidative stress. This stress is a source of the side effects associated with its use. Ellagic acid (EA), a polyphenol is known to possess multiple health benefits owing to its antioxidant properties. EA is largely metabolized by the colon microbiota of different mammals and therefore was a polyphenol of choice in the present study. The present study was thus carried out to explore the protective potential of EA on CP induced hepatotoxicity in colon tumor bearing mice. The administration of EA (10 mg/kg bwt po daily for 6 weeks) significantly ameliorated the toxicity caused by CP (5 mg/kg bwt ip once a week for 4 weeks). Activities of liver marker enzymes and lactate dehydrogenase were brought back to normal. EA cotreatment also led to a marked reduction in the extent of peroxidative damage to liver tissue as was evident from the improvement in the histopathological changes observed and FT-IR analysis. The present study, therefore, suggests that the administration of EA reduces the CP-induced hepatotoxicity, thereby emerging out as a potential candidate for chemopreventive action.

Identifiants

pubmed: 30953405
doi: 10.1002/tox.22747
doi:

Substances chimiques

Antioxidants 0
Polyphenols 0
Reactive Oxygen Species 0
Ellagic Acid 19YRN3ZS9P
Cisplatin Q20Q21Q62J

Types de publication

Journal Article

Langues

eng

Pagination

804-813

Subventions

Organisme : Departmental grant from Panjab University
ID : 15021-15220/A
Organisme : DST-PURSE grant
ID : DST-PURSE-PHASE II-58-60/RPC

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Yasmeen Goyal (Y)

Department of Biophysics, Panjab University, Chandigarh, India.

Ashwani Koul (A)

Department of Biophysics, Panjab University, Chandigarh, India.

Pavitra Ranawat (P)

Department of Biophysics, Panjab University, Chandigarh, India.

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Classifications MeSH