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Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats

BACKGROUND: Osteoporosis, a reduction in bone mineral density, represents the most common metabolic bone disease. Postmenopausal women are particularly susceptible to osteoporosis when their production of estrogen declines. For these women, fracture is a leading cause of morbidity and mortality. Thi...

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Autores principales: Saleh , Nermine K, Saleh , Hanan A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045997/
https://www.ncbi.nlm.nih.gov/pubmed/21294895
http://dx.doi.org/10.1186/1472-6882-11-10
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author Saleh , Nermine K
Saleh , Hanan A
author_facet Saleh , Nermine K
Saleh , Hanan A
author_sort Saleh , Nermine K
collection PubMed
description BACKGROUND: Osteoporosis, a reduction in bone mineral density, represents the most common metabolic bone disease. Postmenopausal women are particularly susceptible to osteoporosis when their production of estrogen declines. For these women, fracture is a leading cause of morbidity and mortality. This study was conducted to evaluate the protective effects of olive oil supplementation against osteoporosis in ovariectomized (OVX) rats. METHODS: We studied adult female Wistar rats aged 12-14 months, divided into three groups: sham-operated control (SHAM), ovariectomized (OVX), and ovariectomized rats supplemented with extravirgin olive oil (Olive-OVX) orally for 12 weeks; 4 weeks before ovariectomy and 8 weeks after. At the end of the experiment, blood samples were collected. Plasma levels of calcium, phosphorus, alkaline phosphatase (ALP), malondialdehyde (MDA), and nitrates were assayed. Specimens from both the tibia and the liver were processed for light microscopic examination. Histomorphometric analysis of the tibia was also performed. RESULTS: The OVX-rats showed a significant decrease in plasma calcium levels, and a significant increase in plasma ALP, MDA, and nitrates levels. These changes were attenuated by olive oil supplementation in the Olive-OVX rats. Light microscopic examination of the tibia of the OVX rats revealed a significant decrease in the cortical bone thickness (CBT) and the trabecular bone thickness (TBT). In addition, there was a significant increase in the osteoclast number denoting bone resorption. In the Olive-OVX rats these parameters were markedly improved as compared to the OVX group. Examination of the liver specimens revealed mononuclear cellular infiltration in the portal areas in the OVX-rats which was not detected in the Olive-OVX rats. CONCLUSIONS: Olive oil effectively mitigated ovariectomy-induced osteoporosis in rats, and is a promising candidate for the treatment of postmenopausal osteoporosis.
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spelling pubmed-30459972011-03-01 Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats Saleh , Nermine K Saleh , Hanan A BMC Complement Altern Med Research Article BACKGROUND: Osteoporosis, a reduction in bone mineral density, represents the most common metabolic bone disease. Postmenopausal women are particularly susceptible to osteoporosis when their production of estrogen declines. For these women, fracture is a leading cause of morbidity and mortality. This study was conducted to evaluate the protective effects of olive oil supplementation against osteoporosis in ovariectomized (OVX) rats. METHODS: We studied adult female Wistar rats aged 12-14 months, divided into three groups: sham-operated control (SHAM), ovariectomized (OVX), and ovariectomized rats supplemented with extravirgin olive oil (Olive-OVX) orally for 12 weeks; 4 weeks before ovariectomy and 8 weeks after. At the end of the experiment, blood samples were collected. Plasma levels of calcium, phosphorus, alkaline phosphatase (ALP), malondialdehyde (MDA), and nitrates were assayed. Specimens from both the tibia and the liver were processed for light microscopic examination. Histomorphometric analysis of the tibia was also performed. RESULTS: The OVX-rats showed a significant decrease in plasma calcium levels, and a significant increase in plasma ALP, MDA, and nitrates levels. These changes were attenuated by olive oil supplementation in the Olive-OVX rats. Light microscopic examination of the tibia of the OVX rats revealed a significant decrease in the cortical bone thickness (CBT) and the trabecular bone thickness (TBT). In addition, there was a significant increase in the osteoclast number denoting bone resorption. In the Olive-OVX rats these parameters were markedly improved as compared to the OVX group. Examination of the liver specimens revealed mononuclear cellular infiltration in the portal areas in the OVX-rats which was not detected in the Olive-OVX rats. CONCLUSIONS: Olive oil effectively mitigated ovariectomy-induced osteoporosis in rats, and is a promising candidate for the treatment of postmenopausal osteoporosis. BioMed Central 2011-02-04 /pmc/articles/PMC3045997/ /pubmed/21294895 http://dx.doi.org/10.1186/1472-6882-11-10 Text en Copyright ©2011 Saleh and Saleh ; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Saleh , Nermine K
Saleh , Hanan A
Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats
title Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats
title_full Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats
title_fullStr Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats
title_full_unstemmed Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats
title_short Olive Oil effectively mitigates ovariectomy-induced osteoporosis in rats
title_sort olive oil effectively mitigates ovariectomy-induced osteoporosis in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045997/
https://www.ncbi.nlm.nih.gov/pubmed/21294895
http://dx.doi.org/10.1186/1472-6882-11-10
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