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Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice

The objective of this study was to evaluate organ-wise toxicological effects of sesamol and determine the LD(50) cut-off value and GHS category following acute oral toxicity method OECD 423. An acute oral toxicity study was carried out in female C57BL/6 mice. Observations for physical behaviour and...

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Autores principales: Khan, Shahanshah, Choudhary, Sandeep, Kumar, Arun, Tripathi, Akanchha Mani, Alok, Amit, Adhikari, Jawahar Singh, Rizvi, Moshahid Alam, Chaudhury, Nabo Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615841/
https://www.ncbi.nlm.nih.gov/pubmed/28959616
http://dx.doi.org/10.1016/j.toxrep.2016.03.005
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author Khan, Shahanshah
Choudhary, Sandeep
Kumar, Arun
Tripathi, Akanchha Mani
Alok, Amit
Adhikari, Jawahar Singh
Rizvi, Moshahid Alam
Chaudhury, Nabo Kumar
author_facet Khan, Shahanshah
Choudhary, Sandeep
Kumar, Arun
Tripathi, Akanchha Mani
Alok, Amit
Adhikari, Jawahar Singh
Rizvi, Moshahid Alam
Chaudhury, Nabo Kumar
author_sort Khan, Shahanshah
collection PubMed
description The objective of this study was to evaluate organ-wise toxicological effects of sesamol and determine the LD(50) cut-off value and GHS category following acute oral toxicity method OECD 423. An acute oral toxicity study was carried out in female C57BL/6 mice. Observations for physical behaviour and measurements on haematology, biochemistry, histology of vital organs were performed. In addition, genotoxicity assessment using comet and micronuclei assays was also performed. Acute toxicological effects were observed at 2000 mg/kg, while no adverse effects observed at 300 mg/kg. The effects of 2000 mg/kg were manifested as severe histopathological changes in all organs (femur, spleen, gastrointestine, lungs, heart, kidney, liver, stomach and brain) and excessive DNA strands breaks occurred in femoral bone marrow cells and splenocytes. A single dose of sesamol (2000 mg/kg, body weight) caused the death of two mice (out of three) within 2 h. Hence, sesamol is in GHS category 4 (>300–2000) with LD(50) cut-off value of 500 mg/kg body weight. In contrast, this study is correlated with the obtained GHS category 4 and LD(50) cut-off value 580 mg/kg body weight by ProTox. In conclusions, the present study has classified sesamol toxicity and assessed organ-wise acute oral toxicity of sesamol in female C57BL/6 mice. Therefore, these findings may be useful for the selection of dosages for further pre-clinical evaluation and potential drug developmental of sesamol.
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spelling pubmed-56158412017-09-28 Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice Khan, Shahanshah Choudhary, Sandeep Kumar, Arun Tripathi, Akanchha Mani Alok, Amit Adhikari, Jawahar Singh Rizvi, Moshahid Alam Chaudhury, Nabo Kumar Toxicol Rep Article The objective of this study was to evaluate organ-wise toxicological effects of sesamol and determine the LD(50) cut-off value and GHS category following acute oral toxicity method OECD 423. An acute oral toxicity study was carried out in female C57BL/6 mice. Observations for physical behaviour and measurements on haematology, biochemistry, histology of vital organs were performed. In addition, genotoxicity assessment using comet and micronuclei assays was also performed. Acute toxicological effects were observed at 2000 mg/kg, while no adverse effects observed at 300 mg/kg. The effects of 2000 mg/kg were manifested as severe histopathological changes in all organs (femur, spleen, gastrointestine, lungs, heart, kidney, liver, stomach and brain) and excessive DNA strands breaks occurred in femoral bone marrow cells and splenocytes. A single dose of sesamol (2000 mg/kg, body weight) caused the death of two mice (out of three) within 2 h. Hence, sesamol is in GHS category 4 (>300–2000) with LD(50) cut-off value of 500 mg/kg body weight. In contrast, this study is correlated with the obtained GHS category 4 and LD(50) cut-off value 580 mg/kg body weight by ProTox. In conclusions, the present study has classified sesamol toxicity and assessed organ-wise acute oral toxicity of sesamol in female C57BL/6 mice. Therefore, these findings may be useful for the selection of dosages for further pre-clinical evaluation and potential drug developmental of sesamol. Elsevier 2016-03-10 /pmc/articles/PMC5615841/ /pubmed/28959616 http://dx.doi.org/10.1016/j.toxrep.2016.03.005 Text en © 2016 Published by Elsevier Ireland Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Khan, Shahanshah
Choudhary, Sandeep
Kumar, Arun
Tripathi, Akanchha Mani
Alok, Amit
Adhikari, Jawahar Singh
Rizvi, Moshahid Alam
Chaudhury, Nabo Kumar
Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice
title Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice
title_full Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice
title_fullStr Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice
title_full_unstemmed Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice
title_short Evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female C57BL/6 mice
title_sort evaluation of sesamol-induced histopathological, biochemical, haematological and genomic alteration after acute oral toxicity in female c57bl/6 mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615841/
https://www.ncbi.nlm.nih.gov/pubmed/28959616
http://dx.doi.org/10.1016/j.toxrep.2016.03.005
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