Ellagic acid ameliorates cisplatin induced hepatotoxicity in colon carcinogenesis.
Animals
Antioxidants
/ pharmacology
Chemical and Drug Induced Liver Injury
/ pathology
Cisplatin
/ adverse effects
Colonic Neoplasms
/ drug therapy
Cytoprotection
/ drug effects
Ellagic Acid
/ pharmacology
Liver
/ drug effects
Liver Function Tests
Male
Mice
Oxidative Stress
/ drug effects
Polyphenols
/ pharmacology
Reactive Oxygen Species
/ metabolism
Spectroscopy, Fourier Transform Infrared
FT-IR
chemotherapy
cisplatin
ellagic acid
hepatotoxicity
Journal
Environmental toxicology
ISSN: 1522-7278
Titre abrégé: Environ Toxicol
Pays: United States
ID NLM: 100885357
Informations de publication
Date de publication:
Jul 2019
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.
Substances chimiques
Antioxidants
0
Polyphenols
0
Reactive Oxygen Species
0
Ellagic Acid
19YRN3ZS9P
Cisplatin
Q20Q21Q62J
Types de publication
Journal Article
Langues
eng
Pagination
804-813Subventions
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.