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Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis

Objective(s): Studies have reported that whole body vibration (WBV) played a vital role in bone remodeling. Circulating serotonin is also involved in negative regulating bone mass in rodents and humans. However, both WBV and inhibition of serotonin biosynthesis may suppress receptor activator of nuc...

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Autores principales: Wei, Qiu-Shi, Huang, Li, Chen, Xian-Hong, Wang, Hai-Bin, Sun, Wei-Shan, Huo., Shao-Chuan, Li, Zi-Qi, Deng, Wei-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938888/
https://www.ncbi.nlm.nih.gov/pubmed/24592309
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author Wei, Qiu-Shi
Huang, Li
Chen, Xian-Hong
Wang, Hai-Bin
Sun, Wei-Shan
Huo., Shao-Chuan
Li, Zi-Qi
Deng, Wei-Min
author_facet Wei, Qiu-Shi
Huang, Li
Chen, Xian-Hong
Wang, Hai-Bin
Sun, Wei-Shan
Huo., Shao-Chuan
Li, Zi-Qi
Deng, Wei-Min
author_sort Wei, Qiu-Shi
collection PubMed
description Objective(s): Studies have reported that whole body vibration (WBV) played a vital role in bone remodeling. Circulating serotonin is also involved in negative regulating bone mass in rodents and humans. However, both WBV and inhibition of serotonin biosynthesis may suppress receptor activator of nuclear factor-kappaB ligand (RANKL)-induced osteoclastogenesis in vitro. The purpose of the current study was to investigate the effect of WBV therapy on the levels of serum serotonin in ovariectomized rats. Materials and Methods: Thirty-six-month-old female Sprague Dawley rats weighing 276.15±37.75 g were ovariectomized to induce osteoporosis, and another ten rats underwent sham operation to establish sham control (SHAM) group. After 3 months, ovariectomized rats were divided into three subgroups and then separately treated with WBV, Alendronate (ALN) and normal saline (OVX), SHAM group was given normal saline. After 6 weeks of treatment, rats were sacrificed. Serum serotonin, RANKL, bone turnover markers, and bone mineral density (BMD), bone strength were evaluated. Results: The serum serotonin level was significantly lower in WBV group than OVX and ALN groups (P<0.05 and P<0.001). RANKL levels significantly decreased in WBV and ALN groups compared to OVX group (P<0.001 for both). BMD and biomechanical parameters of femur significantly increased (P<0.05 for both) and bone turnover levels decreased (P<0.001 for both) in WBV group compared to OVX group. Conclusion: These data indicated that WBV enhanced the bone strength and BMD in ovariectomized rats most likely by reducing the levels of circulating serotonin.
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spelling pubmed-39388882014-03-03 Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis Wei, Qiu-Shi Huang, Li Chen, Xian-Hong Wang, Hai-Bin Sun, Wei-Shan Huo., Shao-Chuan Li, Zi-Qi Deng, Wei-Min Iran J Basic Med Sci Original Article Objective(s): Studies have reported that whole body vibration (WBV) played a vital role in bone remodeling. Circulating serotonin is also involved in negative regulating bone mass in rodents and humans. However, both WBV and inhibition of serotonin biosynthesis may suppress receptor activator of nuclear factor-kappaB ligand (RANKL)-induced osteoclastogenesis in vitro. The purpose of the current study was to investigate the effect of WBV therapy on the levels of serum serotonin in ovariectomized rats. Materials and Methods: Thirty-six-month-old female Sprague Dawley rats weighing 276.15±37.75 g were ovariectomized to induce osteoporosis, and another ten rats underwent sham operation to establish sham control (SHAM) group. After 3 months, ovariectomized rats were divided into three subgroups and then separately treated with WBV, Alendronate (ALN) and normal saline (OVX), SHAM group was given normal saline. After 6 weeks of treatment, rats were sacrificed. Serum serotonin, RANKL, bone turnover markers, and bone mineral density (BMD), bone strength were evaluated. Results: The serum serotonin level was significantly lower in WBV group than OVX and ALN groups (P<0.05 and P<0.001). RANKL levels significantly decreased in WBV and ALN groups compared to OVX group (P<0.001 for both). BMD and biomechanical parameters of femur significantly increased (P<0.05 for both) and bone turnover levels decreased (P<0.001 for both) in WBV group compared to OVX group. Conclusion: These data indicated that WBV enhanced the bone strength and BMD in ovariectomized rats most likely by reducing the levels of circulating serotonin. Mashhad University of Medical Sciences 2014-01 /pmc/articles/PMC3938888/ /pubmed/24592309 Text en © 2014: Iranian Journal of Basic Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Wei, Qiu-Shi
Huang, Li
Chen, Xian-Hong
Wang, Hai-Bin
Sun, Wei-Shan
Huo., Shao-Chuan
Li, Zi-Qi
Deng, Wei-Min
Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis
title Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis
title_full Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis
title_fullStr Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis
title_full_unstemmed Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis
title_short Effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis
title_sort effect of whole body vibration therapy on circulating serotonin levels in an ovariectomized rat model of osteoporosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938888/
https://www.ncbi.nlm.nih.gov/pubmed/24592309
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