High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.

Oxidative stress affects bone turnover. Preventative effects of antioxidants such as vitamin E on reduced bone mineral density and fractures associated with aging, osteoporosis, and smoking have been examined in animals and humans. The effects of vitamin E (α-tocopherol; αT) on bone health have yiel...

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Main Authors: Shunji Kasai, Akemi Ito, Kaori Shindo, Tohru Toyoshi, Masahiro Bando
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4492956?pdf=render
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spelling doaj-ca807b07ef5241cd8ef51a0203c626df2020-11-25T01:21:26ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01107e013205910.1371/journal.pone.0132059High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.Shunji KasaiAkemi ItoKaori ShindoTohru ToyoshiMasahiro BandoOxidative stress affects bone turnover. Preventative effects of antioxidants such as vitamin E on reduced bone mineral density and fractures associated with aging, osteoporosis, and smoking have been examined in animals and humans. The effects of vitamin E (α-tocopherol; αT) on bone health have yielded conflicting and inconclusive results from animal studies. In this study, to determine the bone effects of αT, we investigated the in vivo effects of αT on the bone mineral density, bone mass, bone microstructure, bone resorption, and osteogenesis through peripheral quantitative computed tomography (pQCT) measurements, micro-computed tomography (micro-CT) analyses, and bone histomorphometry of lumbar vertebrae and femurs in normal female Wistar rats fed diets containing αT in different quantities (0, 30, 120, or 600 mg/kg diet) for 8 weeks. To validate our hypotheses regarding bone changes, we examined ovariectomized rats as an osteoporosis model and control sham-operated rats in parallel. As expected, ovariectomized rats had reduced bone mineral density in lumbar vertebrae and the distal metaphyses of their femurs, reduced bone mass and deteriorated microstructure of cancellous bones in the vertebral body and distal femur metaphyses, and reduced bone mass due to resorption-dominant enhanced bone turnover in secondary cancellous bones in these sites. In comparison, αT administered to normal rats, even at the highest dose, did not induce reduced bone mineral density of lumbar vertebrae and femurs or a reduced bone mass or fragile microstructure of cancellous bones of the vertebral body and distal femur metaphyses. Instead, αT-fed rats showed a tendency for an osteogenesis-dominant bone mass increase in secondary cancellous bones in the vertebral body, in which active bone remodeling occurs. Thus, αT consumption may have beneficial effects on bone health.http://europepmc.org/articles/PMC4492956?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Shunji Kasai
Akemi Ito
Kaori Shindo
Tohru Toyoshi
Masahiro Bando
spellingShingle Shunji Kasai
Akemi Ito
Kaori Shindo
Tohru Toyoshi
Masahiro Bando
High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.
PLoS ONE
author_facet Shunji Kasai
Akemi Ito
Kaori Shindo
Tohru Toyoshi
Masahiro Bando
author_sort Shunji Kasai
title High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.
title_short High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.
title_full High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.
title_fullStr High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.
title_full_unstemmed High-Dose α-Tocopherol Supplementation Does Not Induce Bone Loss in Normal Rats.
title_sort high-dose α-tocopherol supplementation does not induce bone loss in normal rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Oxidative stress affects bone turnover. Preventative effects of antioxidants such as vitamin E on reduced bone mineral density and fractures associated with aging, osteoporosis, and smoking have been examined in animals and humans. The effects of vitamin E (α-tocopherol; αT) on bone health have yielded conflicting and inconclusive results from animal studies. In this study, to determine the bone effects of αT, we investigated the in vivo effects of αT on the bone mineral density, bone mass, bone microstructure, bone resorption, and osteogenesis through peripheral quantitative computed tomography (pQCT) measurements, micro-computed tomography (micro-CT) analyses, and bone histomorphometry of lumbar vertebrae and femurs in normal female Wistar rats fed diets containing αT in different quantities (0, 30, 120, or 600 mg/kg diet) for 8 weeks. To validate our hypotheses regarding bone changes, we examined ovariectomized rats as an osteoporosis model and control sham-operated rats in parallel. As expected, ovariectomized rats had reduced bone mineral density in lumbar vertebrae and the distal metaphyses of their femurs, reduced bone mass and deteriorated microstructure of cancellous bones in the vertebral body and distal femur metaphyses, and reduced bone mass due to resorption-dominant enhanced bone turnover in secondary cancellous bones in these sites. In comparison, αT administered to normal rats, even at the highest dose, did not induce reduced bone mineral density of lumbar vertebrae and femurs or a reduced bone mass or fragile microstructure of cancellous bones of the vertebral body and distal femur metaphyses. Instead, αT-fed rats showed a tendency for an osteogenesis-dominant bone mass increase in secondary cancellous bones in the vertebral body, in which active bone remodeling occurs. Thus, αT consumption may have beneficial effects on bone health.
url http://europepmc.org/articles/PMC4492956?pdf=render
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