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Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract

Arsenic created a serious public health problem in Bangladesh due to its presence in groundwater and dissemination of the toxic effects to millions of people. The scarcity of the treatment options to manage this affected population has made the situation much worse. To find a promising treatment opt...

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Autores principales: Barai, Milan, Ahsan, Nazmul, Paul, Nilanjana, Hossain, Khaled, Abdur Rashid, Mohammad, Kato, Masashi, Ohgami, Nobutaka, Azim Akhand, Anwarul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nagoya University 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472542/
https://www.ncbi.nlm.nih.gov/pubmed/28626252
http://dx.doi.org/10.18999/nagjms.79.2.167
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author Barai, Milan
Ahsan, Nazmul
Paul, Nilanjana
Hossain, Khaled
Abdur Rashid, Mohammad
Kato, Masashi
Ohgami, Nobutaka
Azim Akhand, Anwarul
author_facet Barai, Milan
Ahsan, Nazmul
Paul, Nilanjana
Hossain, Khaled
Abdur Rashid, Mohammad
Kato, Masashi
Ohgami, Nobutaka
Azim Akhand, Anwarul
author_sort Barai, Milan
collection PubMed
description Arsenic created a serious public health problem in Bangladesh due to its presence in groundwater and dissemination of the toxic effects to millions of people. The scarcity of the treatment options to manage this affected population has made the situation much worse. To find a promising treatment option, this study was undertaken to examine the ameliorating roles of Syzygium cumini leaf extract (SLE) against arsenic-induced toxic effects in mice. Swiss albino mice were divided into four groups where ‘control’ group received pure water + normal feed, ‘arsenic (As)’ group received sodium arsenite (NaAsO(2))-containing water (10 μg/g body weight/day) + normal feed, ‘As+SLE’ group received NaAsO(2)-containing water + feed supplemented with SLE (50 µg/g body weight/day) and finally the ‘SLE’ group received pure water + feed supplemented with SLE. A gradual increase in body weight gain was observed in control mice; however, the body weight gain in As-exposed mice was decreased. This decrease in body weight gain was prevented in As+SLE group mice that received SLE supplemented feed. Arsenic showed a secondary effect by causing enlargement of spleen, kidney and liver of ‘As’ group mice and this enlargement of the organs was minimized with SLE supplementation. In addition, SLE abrogated arsenic-mediated elevation of serum alkaline phosphatase (ALP), alanine aminotransferase (ALT), lactate dehydrogenase (LDH), uric acid and glucose. These results, therefore, suggest that SLE might have future therapeutic value for preventing or reducing arsenic-induced toxic effects.
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spelling pubmed-54725422017-06-16 Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract Barai, Milan Ahsan, Nazmul Paul, Nilanjana Hossain, Khaled Abdur Rashid, Mohammad Kato, Masashi Ohgami, Nobutaka Azim Akhand, Anwarul Nagoya J Med Sci Original Paper Arsenic created a serious public health problem in Bangladesh due to its presence in groundwater and dissemination of the toxic effects to millions of people. The scarcity of the treatment options to manage this affected population has made the situation much worse. To find a promising treatment option, this study was undertaken to examine the ameliorating roles of Syzygium cumini leaf extract (SLE) against arsenic-induced toxic effects in mice. Swiss albino mice were divided into four groups where ‘control’ group received pure water + normal feed, ‘arsenic (As)’ group received sodium arsenite (NaAsO(2))-containing water (10 μg/g body weight/day) + normal feed, ‘As+SLE’ group received NaAsO(2)-containing water + feed supplemented with SLE (50 µg/g body weight/day) and finally the ‘SLE’ group received pure water + feed supplemented with SLE. A gradual increase in body weight gain was observed in control mice; however, the body weight gain in As-exposed mice was decreased. This decrease in body weight gain was prevented in As+SLE group mice that received SLE supplemented feed. Arsenic showed a secondary effect by causing enlargement of spleen, kidney and liver of ‘As’ group mice and this enlargement of the organs was minimized with SLE supplementation. In addition, SLE abrogated arsenic-mediated elevation of serum alkaline phosphatase (ALP), alanine aminotransferase (ALT), lactate dehydrogenase (LDH), uric acid and glucose. These results, therefore, suggest that SLE might have future therapeutic value for preventing or reducing arsenic-induced toxic effects. Nagoya University 2017-05 /pmc/articles/PMC5472542/ /pubmed/28626252 http://dx.doi.org/10.18999/nagjms.79.2.167 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Paper
Barai, Milan
Ahsan, Nazmul
Paul, Nilanjana
Hossain, Khaled
Abdur Rashid, Mohammad
Kato, Masashi
Ohgami, Nobutaka
Azim Akhand, Anwarul
Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract
title Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract
title_full Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract
title_fullStr Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract
title_full_unstemmed Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract
title_short Amelioration of arsenic-induced toxic effects in mice by dietary supplementation of Syzygium cumini leaf extract
title_sort amelioration of arsenic-induced toxic effects in mice by dietary supplementation of syzygium cumini leaf extract
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472542/
https://www.ncbi.nlm.nih.gov/pubmed/28626252
http://dx.doi.org/10.18999/nagjms.79.2.167
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