Cargando…

Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats

Xian-ling-gu-bao (XLGB) is a well-known patented traditional Chinese prescription widely used to treat osteoporosis, osteoarthritis, aseptic bone necrosis, or climacteric syndrome. However, recent reports have suggested that XLGB may cause liver injury in humans. In the present study, we aimed to ev...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Hao, Zhong, Qingxiang, Wang, Jing, Wang, Man, Fang, Fang, Xia, Zhi, Zhong, Rongling, Huang, Houcai, Ke, Zhongcheng, Wei, Yingjie, Feng, Liang, Shi, Ziqi, Sun, E., Song, Jie, Jia, Xiaobin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438972/
https://www.ncbi.nlm.nih.gov/pubmed/28588485
http://dx.doi.org/10.3389/fphar.2017.00273
_version_ 1783237859325509632
author Wu, Hao
Zhong, Qingxiang
Wang, Jing
Wang, Man
Fang, Fang
Xia, Zhi
Zhong, Rongling
Huang, Houcai
Ke, Zhongcheng
Wei, Yingjie
Feng, Liang
Shi, Ziqi
Sun, E.
Song, Jie
Jia, Xiaobin
author_facet Wu, Hao
Zhong, Qingxiang
Wang, Jing
Wang, Man
Fang, Fang
Xia, Zhi
Zhong, Rongling
Huang, Houcai
Ke, Zhongcheng
Wei, Yingjie
Feng, Liang
Shi, Ziqi
Sun, E.
Song, Jie
Jia, Xiaobin
author_sort Wu, Hao
collection PubMed
description Xian-ling-gu-bao (XLGB) is a well-known patented traditional Chinese prescription widely used to treat osteoporosis, osteoarthritis, aseptic bone necrosis, or climacteric syndrome. However, recent reports have suggested that XLGB may cause liver injury in humans. In the present study, we aimed to evaluate the efficacy of XLGB in the prevention of osteoporosis in the zebrafish and ovariectomized (OVX) rats, both of which have been used as osteoporosis models. The safety of XLGB after long-term administration to OVX rats was also assessed. OVX rats were administered by oral gavage 270 mg/kg (recommended daily dose), 1350 mg/kg, and 1800 mg/kg of XLGB for 26 weeks. Bone mineral density, relative bone surface to bone volume, relative bone volume to total volume, trabecular number, mean trabecular thickness, and mean trabecular spacing in OVX rats were examined at the end of the 26-week dosing period. Additionally, OPG and RANKL expression in the femur were determined by western blot and immunohistochemical staining. To evaluate the safety of XLGB, body weight, hematology, serum biochemistry markers related to toxicology, and organ histopathology were determined in each group of OVX rats. Conversely, the zebrafish was treated with prednisolone to induce osteoporosis in the embryo. Disodium etidronate was used as a treatment control. XLGB was shown to be effective in preventing osteoporosis in both the OVX rats and the prednisolone-treated zebrafish. Similarly, XLGB increased OPG protein and decreased RANKL protein in OVX rats. Interestingly, no obvious toxicity was observed in the heart, liver, kidney, small intestine, or stomach at dosages of up to 1800 mg/kg after treating the OVX rats for 26 weeks. XLGB was shown to be very effective in treating osteoporosis in OVX rats. No obvious toxicity or adverse effects developed in OVX rats at dosages up to 1800 mg/kg, which is equivalent to six times the daily-recommended dose. Therefore, XLGB should be considered a good option for the treatment of post-menopausal osteoporosis.
format Online
Article
Text
id pubmed-5438972
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-54389722017-06-06 Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats Wu, Hao Zhong, Qingxiang Wang, Jing Wang, Man Fang, Fang Xia, Zhi Zhong, Rongling Huang, Houcai Ke, Zhongcheng Wei, Yingjie Feng, Liang Shi, Ziqi Sun, E. Song, Jie Jia, Xiaobin Front Pharmacol Pharmacology Xian-ling-gu-bao (XLGB) is a well-known patented traditional Chinese prescription widely used to treat osteoporosis, osteoarthritis, aseptic bone necrosis, or climacteric syndrome. However, recent reports have suggested that XLGB may cause liver injury in humans. In the present study, we aimed to evaluate the efficacy of XLGB in the prevention of osteoporosis in the zebrafish and ovariectomized (OVX) rats, both of which have been used as osteoporosis models. The safety of XLGB after long-term administration to OVX rats was also assessed. OVX rats were administered by oral gavage 270 mg/kg (recommended daily dose), 1350 mg/kg, and 1800 mg/kg of XLGB for 26 weeks. Bone mineral density, relative bone surface to bone volume, relative bone volume to total volume, trabecular number, mean trabecular thickness, and mean trabecular spacing in OVX rats were examined at the end of the 26-week dosing period. Additionally, OPG and RANKL expression in the femur were determined by western blot and immunohistochemical staining. To evaluate the safety of XLGB, body weight, hematology, serum biochemistry markers related to toxicology, and organ histopathology were determined in each group of OVX rats. Conversely, the zebrafish was treated with prednisolone to induce osteoporosis in the embryo. Disodium etidronate was used as a treatment control. XLGB was shown to be effective in preventing osteoporosis in both the OVX rats and the prednisolone-treated zebrafish. Similarly, XLGB increased OPG protein and decreased RANKL protein in OVX rats. Interestingly, no obvious toxicity was observed in the heart, liver, kidney, small intestine, or stomach at dosages of up to 1800 mg/kg after treating the OVX rats for 26 weeks. XLGB was shown to be very effective in treating osteoporosis in OVX rats. No obvious toxicity or adverse effects developed in OVX rats at dosages up to 1800 mg/kg, which is equivalent to six times the daily-recommended dose. Therefore, XLGB should be considered a good option for the treatment of post-menopausal osteoporosis. Frontiers Media S.A. 2017-05-22 /pmc/articles/PMC5438972/ /pubmed/28588485 http://dx.doi.org/10.3389/fphar.2017.00273 Text en Copyright © 2017 Wu, Zhong, Wang, Wang, Fang, Xia, Zhong, Huang, Ke, Wei, Feng, Shi, Sun, Song and Jia. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Wu, Hao
Zhong, Qingxiang
Wang, Jing
Wang, Man
Fang, Fang
Xia, Zhi
Zhong, Rongling
Huang, Houcai
Ke, Zhongcheng
Wei, Yingjie
Feng, Liang
Shi, Ziqi
Sun, E.
Song, Jie
Jia, Xiaobin
Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats
title Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats
title_full Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats
title_fullStr Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats
title_full_unstemmed Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats
title_short Beneficial Effects and Toxicity Studies of Xian-ling-gu-bao on Bone Metabolism in Ovariectomized Rats
title_sort beneficial effects and toxicity studies of xian-ling-gu-bao on bone metabolism in ovariectomized rats
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438972/
https://www.ncbi.nlm.nih.gov/pubmed/28588485
http://dx.doi.org/10.3389/fphar.2017.00273
work_keys_str_mv AT wuhao beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT zhongqingxiang beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT wangjing beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT wangman beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT fangfang beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT xiazhi beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT zhongrongling beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT huanghoucai beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT kezhongcheng beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT weiyingjie beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT fengliang beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT shiziqi beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT sune beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT songjie beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats
AT jiaxiaobin beneficialeffectsandtoxicitystudiesofxianlinggubaoonbonemetabolisminovariectomizedrats