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Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study

OBJECTIVE: Accelerated bone loss that occurs in postmenopausal women has been linked to oxidative stress and increased free radicals. We propose the use of antioxidants to prevent and reverse postmenopausal osteoporosis. This study aimed to examine the effects of tocotrienol, a vitamin E analog, on...

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Autores principales: Muhammad, Norliza, Luke, Douglas Alwyn, Shuid, Ahmad Nazrun, Mohamed, Norazlina, Soelaiman, Ima Nirwana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798611/
https://www.ncbi.nlm.nih.gov/pubmed/24212841
http://dx.doi.org/10.6061/clinics/2013(10)08
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author Muhammad, Norliza
Luke, Douglas Alwyn
Shuid, Ahmad Nazrun
Mohamed, Norazlina
Soelaiman, Ima Nirwana
author_facet Muhammad, Norliza
Luke, Douglas Alwyn
Shuid, Ahmad Nazrun
Mohamed, Norazlina
Soelaiman, Ima Nirwana
author_sort Muhammad, Norliza
collection PubMed
description OBJECTIVE: Accelerated bone loss that occurs in postmenopausal women has been linked to oxidative stress and increased free radicals. We propose the use of antioxidants to prevent and reverse postmenopausal osteoporosis. This study aimed to examine the effects of tocotrienol, a vitamin E analog, on bone loss due to estrogen deficiency. Our previous study showed that tocotrienol increased the trabecular bone volume and trabecular number in ovariectomized rats. In the current study, we investigated the effects of tocotrienol supplementation on various biochemical parameters in a postmenopausal osteoporosis rat model. MATERIALS AND METHODS: A total of 32 female Wistar rats were randomly divided into four groups. The baseline group was sacrificed at the start of the study, and another group was sham operated. The remaining rats were ovariectomized and either given olive oil as a vehicle or treated with tocotrienol at a dose of 60 mg/kg body weight. After four weeks of treatment, blood was withdrawn for the measurement of interleukin-1 (IL1) and interleukin-6 (IL6) (bone resorbing cytokines), serum osteocalcin (a bone formation marker) and pyridinoline (a bone resorption marker). RESULTS: Tocotrienol supplementation in ovariectomized rats significantly reduced the levels of osteocalcin, IL1 and IL6. However, it did not alter the serum pyridinoline level. CONCLUSION: Tocotrienol prevented osteoporotic bone loss by reducing the high bone turnover rate associated with estrogen deficiency. Therefore, tocotrienol has the potential to be used as an anti-osteoporotic agent in postmenopausal women.
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spelling pubmed-37986112013-10-22 Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study Muhammad, Norliza Luke, Douglas Alwyn Shuid, Ahmad Nazrun Mohamed, Norazlina Soelaiman, Ima Nirwana Clinics (Sao Paulo) Basic Research OBJECTIVE: Accelerated bone loss that occurs in postmenopausal women has been linked to oxidative stress and increased free radicals. We propose the use of antioxidants to prevent and reverse postmenopausal osteoporosis. This study aimed to examine the effects of tocotrienol, a vitamin E analog, on bone loss due to estrogen deficiency. Our previous study showed that tocotrienol increased the trabecular bone volume and trabecular number in ovariectomized rats. In the current study, we investigated the effects of tocotrienol supplementation on various biochemical parameters in a postmenopausal osteoporosis rat model. MATERIALS AND METHODS: A total of 32 female Wistar rats were randomly divided into four groups. The baseline group was sacrificed at the start of the study, and another group was sham operated. The remaining rats were ovariectomized and either given olive oil as a vehicle or treated with tocotrienol at a dose of 60 mg/kg body weight. After four weeks of treatment, blood was withdrawn for the measurement of interleukin-1 (IL1) and interleukin-6 (IL6) (bone resorbing cytokines), serum osteocalcin (a bone formation marker) and pyridinoline (a bone resorption marker). RESULTS: Tocotrienol supplementation in ovariectomized rats significantly reduced the levels of osteocalcin, IL1 and IL6. However, it did not alter the serum pyridinoline level. CONCLUSION: Tocotrienol prevented osteoporotic bone loss by reducing the high bone turnover rate associated with estrogen deficiency. Therefore, tocotrienol has the potential to be used as an anti-osteoporotic agent in postmenopausal women. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2013-10 /pmc/articles/PMC3798611/ /pubmed/24212841 http://dx.doi.org/10.6061/clinics/2013(10)08 Text en Copyright © 2013 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Muhammad, Norliza
Luke, Douglas Alwyn
Shuid, Ahmad Nazrun
Mohamed, Norazlina
Soelaiman, Ima Nirwana
Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study
title Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study
title_full Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study
title_fullStr Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study
title_full_unstemmed Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study
title_short Tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study
title_sort tocotrienol supplementation in postmenopausal osteoporosis: evidence from a laboratory study
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798611/
https://www.ncbi.nlm.nih.gov/pubmed/24212841
http://dx.doi.org/10.6061/clinics/2013(10)08
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