Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluation

The aim of the study was to investigate the protective effect of isoniazid–curcumin conjugate (INH–CRM) in INH-induced hepatic injury by biochemical analysis and histology examination of liver in Wistar rats. The biochemical analysis included determination of the levels of plasma cholesterol, trigly...

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Main Authors: Charan Singh, Laxmikant Jodave, Tara Datt Bhatt, Manjinder Singh Gill, Sarasija Suresh
Format: Article
Language:English
Published: Elsevier 2014-01-01
Series:Toxicology Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2214750014000985
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author Charan Singh
Laxmikant Jodave
Tara Datt Bhatt
Manjinder Singh Gill
Sarasija Suresh
author_facet Charan Singh
Laxmikant Jodave
Tara Datt Bhatt
Manjinder Singh Gill
Sarasija Suresh
author_sort Charan Singh
collection DOAJ
description The aim of the study was to investigate the protective effect of isoniazid–curcumin conjugate (INH–CRM) in INH-induced hepatic injury by biochemical analysis and histology examination of liver in Wistar rats. The biochemical analysis included determination of the levels of plasma cholesterol, triglycerides (TG), albumin content, and lipid peroxidation (MDA). INH–CRM administration resulted in a significant decrease in plasma cholesterol, TG, and MDA levels in the liver tissue homogenate with an elevation in albumin level indicating its hepatoprotective activity. Histology of the liver further confirmed the reduction in hepatic injury. The hepatoprotective with INH–CRM can be attributed to the antioxidant activity of curcumin. The conjugate probably stabilizes the curcumin molecule, preventing its presystemic metabolism thereby enhancing its bioavailability and therefore, its hepatoprotective activity. Thus, the novel INH–CRM has the potential to alleviate INH-induced liver toxicity in antitubercular treatment.
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spelling doaj.art-654f26d71b034aa4a94776b01d98c5712022-12-21T19:19:55ZengElsevierToxicology Reports2214-75002014-01-011C88589310.1016/j.toxrep.2014.10.001Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluationCharan Singh0Laxmikant Jodave1Tara Datt Bhatt2Manjinder Singh Gill3Sarasija Suresh4Department of Pharmaceutical Technology (Formulations), National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S.A.S. Nagar (Mohali) Punjab 160062 IndiaDepartment of Pharmaceutical Technology (Formulations), National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S.A.S. Nagar (Mohali) Punjab 160062 IndiaTechnology Development Centre, National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S.A.S. Nagar (Mohali) Punjab 160062 IndiaDepartment of Pharmaceutical Technology (Process Chemistry), National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S.A.S. Nagar (Mohali) Punjab160062 IndiaDepartment of Pharmaceutical Technology (Formulations), National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S.A.S. Nagar (Mohali) Punjab 160062 IndiaThe aim of the study was to investigate the protective effect of isoniazid–curcumin conjugate (INH–CRM) in INH-induced hepatic injury by biochemical analysis and histology examination of liver in Wistar rats. The biochemical analysis included determination of the levels of plasma cholesterol, triglycerides (TG), albumin content, and lipid peroxidation (MDA). INH–CRM administration resulted in a significant decrease in plasma cholesterol, TG, and MDA levels in the liver tissue homogenate with an elevation in albumin level indicating its hepatoprotective activity. Histology of the liver further confirmed the reduction in hepatic injury. The hepatoprotective with INH–CRM can be attributed to the antioxidant activity of curcumin. The conjugate probably stabilizes the curcumin molecule, preventing its presystemic metabolism thereby enhancing its bioavailability and therefore, its hepatoprotective activity. Thus, the novel INH–CRM has the potential to alleviate INH-induced liver toxicity in antitubercular treatment.http://www.sciencedirect.com/science/article/pii/S2214750014000985
spellingShingle Charan Singh
Laxmikant Jodave
Tara Datt Bhatt
Manjinder Singh Gill
Sarasija Suresh
Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluation
Toxicology Reports
title Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluation
title_full Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluation
title_fullStr Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluation
title_full_unstemmed Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluation
title_short Hepatoprotective agent tethered isoniazid for the treatment of drug-induced hepatotoxicity: Synthesis, biochemical and histopathological evaluation
title_sort hepatoprotective agent tethered isoniazid for the treatment of drug induced hepatotoxicity synthesis biochemical and histopathological evaluation
url http://www.sciencedirect.com/science/article/pii/S2214750014000985
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AT laxmikantjodave hepatoprotectiveagenttetheredisoniazidforthetreatmentofdruginducedhepatotoxicitysynthesisbiochemicalandhistopathologicalevaluation
AT taradattbhatt hepatoprotectiveagenttetheredisoniazidforthetreatmentofdruginducedhepatotoxicitysynthesisbiochemicalandhistopathologicalevaluation
AT manjindersinghgill hepatoprotectiveagenttetheredisoniazidforthetreatmentofdruginducedhepatotoxicitysynthesisbiochemicalandhistopathologicalevaluation
AT sarasijasuresh hepatoprotectiveagenttetheredisoniazidforthetreatmentofdruginducedhepatotoxicitysynthesisbiochemicalandhistopathologicalevaluation