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Vitamin E improved bone strength and bone minerals in male rats given alcohol

OBJECTIVE(S): Alcohol consumption induces oxidative stress on bone, which in turn increases the risk of osteoporosis. This study determined the effects of vitamin E on bone strength and bone mineral content in alcohol-induced osteoporotic rats. MATERIALS AND METHODS: Three months old Sprague Dawley...

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Autores principales: Zakaria, Syuhada, Mat-Husain, Siti-Zulaikha, Ying-Hwey, Kong, Xin-Kai, Kek, Mohd-Badawi, Abdullah, Abd-Ghani, Nurul-Amiza, Aziz, Muhamad-Arizi, Mohamed, Norazlina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722997/
https://www.ncbi.nlm.nih.gov/pubmed/29238472
http://dx.doi.org/10.22038/IJBMS.2017.9610
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author Zakaria, Syuhada
Mat-Husain, Siti-Zulaikha
Ying-Hwey, Kong
Xin-Kai, Kek
Mohd-Badawi, Abdullah
Abd-Ghani, Nurul-Amiza
Aziz, Muhamad-Arizi
Mohamed, Norazlina
author_facet Zakaria, Syuhada
Mat-Husain, Siti-Zulaikha
Ying-Hwey, Kong
Xin-Kai, Kek
Mohd-Badawi, Abdullah
Abd-Ghani, Nurul-Amiza
Aziz, Muhamad-Arizi
Mohamed, Norazlina
author_sort Zakaria, Syuhada
collection PubMed
description OBJECTIVE(S): Alcohol consumption induces oxidative stress on bone, which in turn increases the risk of osteoporosis. This study determined the effects of vitamin E on bone strength and bone mineral content in alcohol-induced osteoporotic rats. MATERIALS AND METHODS: Three months old Sprague Dawley male rats were randomly divided into 5 groups: (I) control group; (II) alcohol (3g/kg) + normal saline; (III) alcohol (3g/kg) + olive oil; (IV) alcohol (3g/kg) + alpha-tocopherol (60mg/kg) and (V) alcohol (3g/kg) + palm vitamin E (60mg/kg). The treatment lasted for three months. Following sacrifice, the right tibia was subjected to bone biomechanical test while the lumbar (fourth and fifth lumbar) and left tibia bones were harvested for bone mineral measurement. RESULTS: Alcohol caused reduction in bone biomechanical parameters (maximum force, ultimate stress, yield stress and Young’s modulus) and bone minerals (bone calcium and magnesium) compared to control group (P<0.05). Palm vitamin E was able to improve bone biomechanical parameters by increasing the maximum force, ultimate stress and Young’s modulus (P<0.05) while alpha-tocopherol was not able to. Both alpha-tocopherol and palm vitamin E were able to significantly increase tibia calcium and magnesium content while only alpha-tocopherol caused significant increase in lumbar calcium content (P<0.05). CONCLUSION: Both palm vitamin E and alpha-tocopherol improved bone mineral content which was reduced by alcohol. However, only palm vitamin E was able to improve bone strength in alcohol treated rats.
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spelling pubmed-57229972017-12-13 Vitamin E improved bone strength and bone minerals in male rats given alcohol Zakaria, Syuhada Mat-Husain, Siti-Zulaikha Ying-Hwey, Kong Xin-Kai, Kek Mohd-Badawi, Abdullah Abd-Ghani, Nurul-Amiza Aziz, Muhamad-Arizi Mohamed, Norazlina Iran J Basic Med Sci Original Article OBJECTIVE(S): Alcohol consumption induces oxidative stress on bone, which in turn increases the risk of osteoporosis. This study determined the effects of vitamin E on bone strength and bone mineral content in alcohol-induced osteoporotic rats. MATERIALS AND METHODS: Three months old Sprague Dawley male rats were randomly divided into 5 groups: (I) control group; (II) alcohol (3g/kg) + normal saline; (III) alcohol (3g/kg) + olive oil; (IV) alcohol (3g/kg) + alpha-tocopherol (60mg/kg) and (V) alcohol (3g/kg) + palm vitamin E (60mg/kg). The treatment lasted for three months. Following sacrifice, the right tibia was subjected to bone biomechanical test while the lumbar (fourth and fifth lumbar) and left tibia bones were harvested for bone mineral measurement. RESULTS: Alcohol caused reduction in bone biomechanical parameters (maximum force, ultimate stress, yield stress and Young’s modulus) and bone minerals (bone calcium and magnesium) compared to control group (P<0.05). Palm vitamin E was able to improve bone biomechanical parameters by increasing the maximum force, ultimate stress and Young’s modulus (P<0.05) while alpha-tocopherol was not able to. Both alpha-tocopherol and palm vitamin E were able to significantly increase tibia calcium and magnesium content while only alpha-tocopherol caused significant increase in lumbar calcium content (P<0.05). CONCLUSION: Both palm vitamin E and alpha-tocopherol improved bone mineral content which was reduced by alcohol. However, only palm vitamin E was able to improve bone strength in alcohol treated rats. Mashhad University of Medical Sciences 2017-12 /pmc/articles/PMC5722997/ /pubmed/29238472 http://dx.doi.org/10.22038/IJBMS.2017.9610 Text en Copyright: © Iranian Journal of Basic Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zakaria, Syuhada
Mat-Husain, Siti-Zulaikha
Ying-Hwey, Kong
Xin-Kai, Kek
Mohd-Badawi, Abdullah
Abd-Ghani, Nurul-Amiza
Aziz, Muhamad-Arizi
Mohamed, Norazlina
Vitamin E improved bone strength and bone minerals in male rats given alcohol
title Vitamin E improved bone strength and bone minerals in male rats given alcohol
title_full Vitamin E improved bone strength and bone minerals in male rats given alcohol
title_fullStr Vitamin E improved bone strength and bone minerals in male rats given alcohol
title_full_unstemmed Vitamin E improved bone strength and bone minerals in male rats given alcohol
title_short Vitamin E improved bone strength and bone minerals in male rats given alcohol
title_sort vitamin e improved bone strength and bone minerals in male rats given alcohol
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722997/
https://www.ncbi.nlm.nih.gov/pubmed/29238472
http://dx.doi.org/10.22038/IJBMS.2017.9610
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