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Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry

A total of 225 day-old sexed male broiler chicks (Vencobb strain) were divided randomly into 15 groups consisting of 15 chicks in each group to study the toxicity of lead on hepatocytes. Group 1 was maintained on basal diet, group 2 on polyherbal formulation (PHF; stressroak), group 3 on shilajith,...

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Autores principales: Kumar, M. Ratan, Reddy, K. S., Reddy, A. Gopala, Reddy, Rajasekhar A., Anjaneyulu, Y., Reddy, Dilip G.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052589/
https://www.ncbi.nlm.nih.gov/pubmed/21430925
http://dx.doi.org/10.4103/0971-6580.75866
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author Kumar, M. Ratan
Reddy, K. S.
Reddy, A. Gopala
Reddy, Rajasekhar A.
Anjaneyulu, Y.
Reddy, Dilip G.
author_facet Kumar, M. Ratan
Reddy, K. S.
Reddy, A. Gopala
Reddy, Rajasekhar A.
Anjaneyulu, Y.
Reddy, Dilip G.
author_sort Kumar, M. Ratan
collection PubMed
description A total of 225 day-old sexed male broiler chicks (Vencobb strain) were divided randomly into 15 groups consisting of 15 chicks in each group to study the toxicity of lead on hepatocytes. Group 1 was maintained on basal diet, group 2 on polyherbal formulation (PHF; stressroak), group 3 on shilajith, group 4 on amla and group 5 on vit E + Se. Group 6 was maintained on lead for 6 weeks and group 7 on lead for 4 weeks and subsequently on basal diet without lead for the remaining 2 weeks. Groups 8, 9, 10 and 11 were given lead along with PHF, shilajith, amla and vit E + Se, respectively, throughout 6 weeks. Groups 12, 13, 14 and 15 were given lead containing diet for the first 4 weeks and subsequently treated with PHF, shilajith, amla and vit E + Se, respectively, for the remaining 2 weeks. The activity of alanine transaminase (ALT) was significantly (P<0.05) increased in the toxic control groups at the end of 4(th) week as compared to group 1. However, following treatment, there was a significant (P<0.05) reversal in groups 12–15. The activity of Na(+)/K(+)-ATPase, Ca(2+)ATPase, Mg(2+)ATPase and CYP(450) was significantly (P<0.05) reduced in the liver of toxic control groups 6 and 7 as compared to groups1 through 5, which had the maximum activity of all the groups. Groups 8 through 15 revealed a significant (P<0.05) increase in the activity of these hepatocytic enzymes. The histological sections of the liver in lead toxic control (group 6) showed moderate focal lymphoid aggregates in liver, whereas the lesions were mild to moderate in treated groups and there were no observable lesions in plain control groups. The study revealed protective effect of PHF (stressroak), shilajith, amla and vit E + Se in lead-induced hepatocytic damage.
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spelling pubmed-30525892011-03-22 Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry Kumar, M. Ratan Reddy, K. S. Reddy, A. Gopala Reddy, Rajasekhar A. Anjaneyulu, Y. Reddy, Dilip G. Toxicol Int Original Article A total of 225 day-old sexed male broiler chicks (Vencobb strain) were divided randomly into 15 groups consisting of 15 chicks in each group to study the toxicity of lead on hepatocytes. Group 1 was maintained on basal diet, group 2 on polyherbal formulation (PHF; stressroak), group 3 on shilajith, group 4 on amla and group 5 on vit E + Se. Group 6 was maintained on lead for 6 weeks and group 7 on lead for 4 weeks and subsequently on basal diet without lead for the remaining 2 weeks. Groups 8, 9, 10 and 11 were given lead along with PHF, shilajith, amla and vit E + Se, respectively, throughout 6 weeks. Groups 12, 13, 14 and 15 were given lead containing diet for the first 4 weeks and subsequently treated with PHF, shilajith, amla and vit E + Se, respectively, for the remaining 2 weeks. The activity of alanine transaminase (ALT) was significantly (P<0.05) increased in the toxic control groups at the end of 4(th) week as compared to group 1. However, following treatment, there was a significant (P<0.05) reversal in groups 12–15. The activity of Na(+)/K(+)-ATPase, Ca(2+)ATPase, Mg(2+)ATPase and CYP(450) was significantly (P<0.05) reduced in the liver of toxic control groups 6 and 7 as compared to groups1 through 5, which had the maximum activity of all the groups. Groups 8 through 15 revealed a significant (P<0.05) increase in the activity of these hepatocytic enzymes. The histological sections of the liver in lead toxic control (group 6) showed moderate focal lymphoid aggregates in liver, whereas the lesions were mild to moderate in treated groups and there were no observable lesions in plain control groups. The study revealed protective effect of PHF (stressroak), shilajith, amla and vit E + Se in lead-induced hepatocytic damage. Medknow Publications 2011 /pmc/articles/PMC3052589/ /pubmed/21430925 http://dx.doi.org/10.4103/0971-6580.75866 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
Kumar, M. Ratan
Reddy, K. S.
Reddy, A. Gopala
Reddy, Rajasekhar A.
Anjaneyulu, Y.
Reddy, Dilip G.
Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry
title Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry
title_full Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry
title_fullStr Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry
title_full_unstemmed Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry
title_short Lead-induced Hepatotoxicity and Evaluation of Certain Anti-stress Adaptogens in Poultry
title_sort lead-induced hepatotoxicity and evaluation of certain anti-stress adaptogens in poultry
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052589/
https://www.ncbi.nlm.nih.gov/pubmed/21430925
http://dx.doi.org/10.4103/0971-6580.75866
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