Cargando…

The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice

Livergol (LG), which is the extract of Silybum marianum and commonly known as milk thistle possess hepatoprotective effect and have got licensed for sale in Iran and other countries. LG was evaluated for its capacity to counteract the toxic effects of bromobenzene (BB) on mouse liver. The bioactive...

Descripción completa

Detalles Bibliográficos
Autores principales: Kalantari, Azin, Salimi, Anayatollah, Kalantari, Heibatullah, Ebrahimi Broojeni, Jalal, Rashidi, Iran, Raesi Vanani, Atefeh, Bácskay, Ildikó
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529715/
https://www.ncbi.nlm.nih.gov/pubmed/31193476
http://dx.doi.org/10.1016/j.toxrep.2019.05.005
_version_ 1783420462797160448
author Kalantari, Azin
Salimi, Anayatollah
Kalantari, Heibatullah
Ebrahimi Broojeni, Jalal
Rashidi, Iran
Raesi Vanani, Atefeh
Bácskay, Ildikó
author_facet Kalantari, Azin
Salimi, Anayatollah
Kalantari, Heibatullah
Ebrahimi Broojeni, Jalal
Rashidi, Iran
Raesi Vanani, Atefeh
Bácskay, Ildikó
author_sort Kalantari, Azin
collection PubMed
description Livergol (LG), which is the extract of Silybum marianum and commonly known as milk thistle possess hepatoprotective effect and have got licensed for sale in Iran and other countries. LG was evaluated for its capacity to counteract the toxic effects of bromobenzene (BB) on mouse liver. The bioactive component of this plant is known to reinforce naturally occurring liver function through antioxidant activity, the stimulation of bile production and regeneration by the liver organ, resulting in enhanced protection against toxicants, hepatitis, and cirrhosis. The major bioactive components of this product are the flavonolignan ssilibinin, silidianin, silicristin, and isosilibinin. Mice were treated for 10 days with daily gavage of microemulsions (MEs), into which 0–400 mg/kg LG was dispersed. 0.36 ml/kg BB was injected intraperitoneally (ip) to each animal on day 10, followed by sacrifice on day 11, and histological evaluation of hematoxylin-eosin (HE)‐stained liver tissue samples, afterwards followed by evaluation liver enzymes level, aminotransferase (AST), alanine aminotransaminase (ALT) and alkaline phosphatase (ALP) activities. Significant suppression of BB-mediated damage to liver tissue, and increased in AST, ALT, and ALP level was observed to occur dose-responsively with LG administration, suggesting a use for LG as a chemoprotectant for persons chronically exposed to industrial solvents.
format Online
Article
Text
id pubmed-6529715
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-65297152019-05-28 The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice Kalantari, Azin Salimi, Anayatollah Kalantari, Heibatullah Ebrahimi Broojeni, Jalal Rashidi, Iran Raesi Vanani, Atefeh Bácskay, Ildikó Toxicol Rep Article Livergol (LG), which is the extract of Silybum marianum and commonly known as milk thistle possess hepatoprotective effect and have got licensed for sale in Iran and other countries. LG was evaluated for its capacity to counteract the toxic effects of bromobenzene (BB) on mouse liver. The bioactive component of this plant is known to reinforce naturally occurring liver function through antioxidant activity, the stimulation of bile production and regeneration by the liver organ, resulting in enhanced protection against toxicants, hepatitis, and cirrhosis. The major bioactive components of this product are the flavonolignan ssilibinin, silidianin, silicristin, and isosilibinin. Mice were treated for 10 days with daily gavage of microemulsions (MEs), into which 0–400 mg/kg LG was dispersed. 0.36 ml/kg BB was injected intraperitoneally (ip) to each animal on day 10, followed by sacrifice on day 11, and histological evaluation of hematoxylin-eosin (HE)‐stained liver tissue samples, afterwards followed by evaluation liver enzymes level, aminotransferase (AST), alanine aminotransaminase (ALT) and alkaline phosphatase (ALP) activities. Significant suppression of BB-mediated damage to liver tissue, and increased in AST, ALT, and ALP level was observed to occur dose-responsively with LG administration, suggesting a use for LG as a chemoprotectant for persons chronically exposed to industrial solvents. Elsevier 2019-05-09 /pmc/articles/PMC6529715/ /pubmed/31193476 http://dx.doi.org/10.1016/j.toxrep.2019.05.005 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kalantari, Azin
Salimi, Anayatollah
Kalantari, Heibatullah
Ebrahimi Broojeni, Jalal
Rashidi, Iran
Raesi Vanani, Atefeh
Bácskay, Ildikó
The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice
title The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice
title_full The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice
title_fullStr The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice
title_full_unstemmed The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice
title_short The hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice
title_sort hepatoprotective effect of livergol microemulsion preparation (nanoparticle) against bromobenzene induced toxicity in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529715/
https://www.ncbi.nlm.nih.gov/pubmed/31193476
http://dx.doi.org/10.1016/j.toxrep.2019.05.005
work_keys_str_mv AT kalantariazin thehepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT salimianayatollah thehepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT kalantariheibatullah thehepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT ebrahimibroojenijalal thehepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT rashidiiran thehepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT raesivananiatefeh thehepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT bacskayildiko thehepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT kalantariazin hepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT salimianayatollah hepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT kalantariheibatullah hepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT ebrahimibroojenijalal hepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT rashidiiran hepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT raesivananiatefeh hepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice
AT bacskayildiko hepatoprotectiveeffectoflivergolmicroemulsionpreparationnanoparticleagainstbromobenzeneinducedtoxicityinmice