Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of Osteopenia
Background. 8-Prenylnaringenin (8-PN) is the phytoestrogen with the highest affinity for estrogen receptor-α (ER-α), which is required to maintain BMD. The osteoprotective properties of 8-PN have been demonstrated previously in tibiae. We used a rat osteopenia model to perform the first investigatio...
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doaj-e4545901512745c1a6cc2498a09112ae2020-11-24T23:02:53ZengHindawi LimitedJournal of Nutrition and Metabolism2090-07242090-07322016-01-01201610.1155/2016/68931376893137Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of OsteopeniaDaniel B. Hoffmann0Markus H. Griesel1Bastian Brockhusen2Mohammad Tezval3Marina Komrakova4Bjoern Menger5Marco Wassmann6Klaus Michael Stuermer7Stephan Sehmisch8Department of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyDepartment of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyDepartment of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyDepartment of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyDepartment of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyDepartment of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyMedical Institute of General Hygiene and Environmental Health, University of Goettingen, 37075 Goettingen, GermanyDepartment of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyDepartment of Trauma and Reconstructive Surgery, University of Goettingen, 37075 Goettingen, GermanyBackground. 8-Prenylnaringenin (8-PN) is the phytoestrogen with the highest affinity for estrogen receptor-α (ER-α), which is required to maintain BMD. The osteoprotective properties of 8-PN have been demonstrated previously in tibiae. We used a rat osteopenia model to perform the first investigation of 8-PN with whole-body vertical vibration (WBVV). Study Design. Ovariectomy was performed on 52 of 64 Sprague-Dawley rats. Five weeks after ovariectomy, one group received daily injections (sc) of 8-PN (1.77 mg/kg) for 10 weeks; a second group was treated with both 8-PN and WBVV (twice a day, 15 min, 35 Hz, amplitude 0.47 mm). Other groups received either only WBVV or no treatment. Methods. The rats were sacrificed 15 weeks after ovariectomy. Lumbar vertebrae and femora were removed for biomechanical and morphological assessment. Results. 8-PN at a cancer-safe dose did not cause fundamental improvements in osteoporotic bones. Treatment with 8-PN caused a slight increase in uterine wet weight. Combined therapy using WBVV and 8-PN showed no significant improvements in bone structure and biomechanical properties. Conclusion. We cannot confirm the osteoprotective effects of 8-PN at a cancer-safe dose in primary affected osteoporotic bones. Higher concentrations of 8-PN are not advisable for safety reasons. Adjunctive therapy with WBVV demonstrates no convincing effects on bones.http://dx.doi.org/10.1155/2016/6893137 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Daniel B. Hoffmann Markus H. Griesel Bastian Brockhusen Mohammad Tezval Marina Komrakova Bjoern Menger Marco Wassmann Klaus Michael Stuermer Stephan Sehmisch |
spellingShingle |
Daniel B. Hoffmann Markus H. Griesel Bastian Brockhusen Mohammad Tezval Marina Komrakova Bjoern Menger Marco Wassmann Klaus Michael Stuermer Stephan Sehmisch Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of Osteopenia Journal of Nutrition and Metabolism |
author_facet |
Daniel B. Hoffmann Markus H. Griesel Bastian Brockhusen Mohammad Tezval Marina Komrakova Bjoern Menger Marco Wassmann Klaus Michael Stuermer Stephan Sehmisch |
author_sort |
Daniel B. Hoffmann |
title |
Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of Osteopenia |
title_short |
Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of Osteopenia |
title_full |
Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of Osteopenia |
title_fullStr |
Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of Osteopenia |
title_full_unstemmed |
Effects of 8-Prenylnaringenin and Whole-Body Vibration Therapy on a Rat Model of Osteopenia |
title_sort |
effects of 8-prenylnaringenin and whole-body vibration therapy on a rat model of osteopenia |
publisher |
Hindawi Limited |
series |
Journal of Nutrition and Metabolism |
issn |
2090-0724 2090-0732 |
publishDate |
2016-01-01 |
description |
Background. 8-Prenylnaringenin (8-PN) is the phytoestrogen with the highest affinity for estrogen receptor-α (ER-α), which is required to maintain BMD. The osteoprotective properties of 8-PN have been demonstrated previously in tibiae. We used a rat osteopenia model to perform the first investigation of 8-PN with whole-body vertical vibration (WBVV). Study Design. Ovariectomy was performed on 52 of 64 Sprague-Dawley rats. Five weeks after ovariectomy, one group received daily injections (sc) of 8-PN (1.77 mg/kg) for 10 weeks; a second group was treated with both 8-PN and WBVV (twice a day, 15 min, 35 Hz, amplitude 0.47 mm). Other groups received either only WBVV or no treatment. Methods. The rats were sacrificed 15 weeks after ovariectomy. Lumbar vertebrae and femora were removed for biomechanical and morphological assessment. Results. 8-PN at a cancer-safe dose did not cause fundamental improvements in osteoporotic bones. Treatment with 8-PN caused a slight increase in uterine wet weight. Combined therapy using WBVV and 8-PN showed no significant improvements in bone structure and biomechanical properties. Conclusion. We cannot confirm the osteoprotective effects of 8-PN at a cancer-safe dose in primary affected osteoporotic bones. Higher concentrations of 8-PN are not advisable for safety reasons. Adjunctive therapy with WBVV demonstrates no convincing effects on bones. |
url |
http://dx.doi.org/10.1155/2016/6893137 |
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