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Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats

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 s...

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Autores principales: Gopi, K. S., Reddy, A. Gopala, Jyothi, K., Kumar, B. Anil
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2997457/
https://www.ncbi.nlm.nih.gov/pubmed/21170247
http://dx.doi.org/10.4103/0971-6580.72672
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author Gopi, K. S.
Reddy, A. Gopala
Jyothi, K.
Kumar, B. Anil
author_facet Gopi, K. S.
Reddy, A. Gopala
Jyothi, K.
Kumar, B. Anil
author_sort Gopi, K. S.
collection PubMed
description 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.
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spelling pubmed-29974572010-12-17 Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats Gopi, K. S. Reddy, A. Gopala Jyothi, K. Kumar, B. Anil Toxicol Int Original Article 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. Medknow Publications 2010 /pmc/articles/PMC2997457/ /pubmed/21170247 http://dx.doi.org/10.4103/0971-6580.72672 Text en © Toxicology International http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gopi, K. S.
Reddy, A. Gopala
Jyothi, K.
Kumar, B. Anil
Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats
title Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats
title_full Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats
title_fullStr Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats
title_full_unstemmed Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats
title_short Acetaminophen-induced Hepato- and Nephrotoxicity and Amelioration by Silymarin and Terminalia chebula in Rats
title_sort acetaminophen-induced hepato- and nephrotoxicity and amelioration by silymarin and terminalia chebula in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2997457/
https://www.ncbi.nlm.nih.gov/pubmed/21170247
http://dx.doi.org/10.4103/0971-6580.72672
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