Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by silymarin and Terminalia chebula in rats
Author(s) -
A. Gopala Reddy,
Kanagaraj Jyothi,
Anil Kumar Banothu,
KS Gopi
Publication year - 2010
Publication title -
toxicology international
Language(s) - English
Resource type - Journals
eISSN - 0976-5131
pISSN - 0971-6580
DOI - 10.4103/0971-6580.72672
Subject(s) - terminalia chebula , nephrotoxicity , blood urea nitrogen , creatinine , pharmacology , toxicity , acetaminophen , aspartate transaminase , oral administration , chemistry , urine , medicine , traditional medicine , alkaline phosphatase , biochemistry , enzyme
Experimental study was conducted to evaluate the hepato- and renoprotective effect of silymarin and Terminalia chebula against experimentally-induced acetaminophen (APAP) toxicity in rats. Oral administration of APAP @ 500 mg/kg for 1 to 3 days to all the four groups (six rats in each) resulted in significant elevation of serum triglycerides, total cholesterol, blood urea nitrogen, serum creatinine, and aspartate transaminase activity. Post-treatment with silymarin @ 25 mg/kg and T. chebula 125 mg/kg in groups 2 and 3 and their combination to group 4 from day 4 to 14 has significantly reversed the alterations of above said markers and offered better protection. The results of the study enunciated that silymarin and T. chebula exhibit good hepato- and nephro-protection against APAP toxicity.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom