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Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice)
OBJECTIVES: The purpose of this study is to evaluate the effects of teriparatide (TPTD) on bone mineral density (BMD), bone strength, and bone quality in Akita mouse models of diabetes mellitus. METHODS: Twelve-week-old female Akita mice and control mice (C57/BL/6NCrSlc) were divided into 4 groups:...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Osteoporosis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953529/ https://www.ncbi.nlm.nih.gov/pubmed/31938729 http://dx.doi.org/10.1016/j.afos.2019.11.003 |
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author | Ohuchi, Kentaro Miyakoshi, Naohisa Kasukawa, Yuji Segawa, Toyohito Kinoshita, Hayato Sato, Chie Fujii, Masashi Shimada, Yoichi |
author_facet | Ohuchi, Kentaro Miyakoshi, Naohisa Kasukawa, Yuji Segawa, Toyohito Kinoshita, Hayato Sato, Chie Fujii, Masashi Shimada, Yoichi |
author_sort | Ohuchi, Kentaro |
collection | PubMed |
description | OBJECTIVES: The purpose of this study is to evaluate the effects of teriparatide (TPTD) on bone mineral density (BMD), bone strength, and bone quality in Akita mouse models of diabetes mellitus. METHODS: Twelve-week-old female Akita mice and control mice (C57/BL/6NCrSlc) were divided into 4 groups: control mice treated with vehicle (n = 7) or TPTD (n = 6); and Akita mice treated with vehicle (n = 6) or TPTD (n = 7). TPTD or vehicle was administered subcutaneously 3 times a week for 8 weeks. Blood glucose, serum sclerostin, total tibial BMD, femoral shaft bone strength, and bone quality using Fourier-transform infrared spectroscopy imaging were evaluated. RESULTS: No significant differences in serum sclerostin levels were evident among these groups after 8 weeks of treatment. TPTD significantly increased BMD in control mice (+12.7%, P = 0.02) and Akita mice (+29.2%, P = 0.001) compared with vehicle. Maximum load and stiffness were significantly higher in Akita mice treated with TPTD than in Akita mice treated with vehicle (+56.6%, P = 0.03 and + 90.5%, P = 0.02, respectively). On Fourier-transform infrared spectroscopy imaging, the mineral/matrix ratio was significantly lower in Akita mice treated with vehicle than in control mice (−12.2%, P = 0.02), and TPTD treatment significantly increased the mineral/matrix ratio (P = 0.003). CONCLUSIONS: TPTD thus improved BMD and bone strength in both control mice and Akita mice, with improvements in the mineral/matrix ratio among Akita mice. |
format | Online Article Text |
id | pubmed-6953529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society of Osteoporosis |
record_format | MEDLINE/PubMed |
spelling | pubmed-69535292020-01-14 Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice) Ohuchi, Kentaro Miyakoshi, Naohisa Kasukawa, Yuji Segawa, Toyohito Kinoshita, Hayato Sato, Chie Fujii, Masashi Shimada, Yoichi Osteoporos Sarcopenia Original Article OBJECTIVES: The purpose of this study is to evaluate the effects of teriparatide (TPTD) on bone mineral density (BMD), bone strength, and bone quality in Akita mouse models of diabetes mellitus. METHODS: Twelve-week-old female Akita mice and control mice (C57/BL/6NCrSlc) were divided into 4 groups: control mice treated with vehicle (n = 7) or TPTD (n = 6); and Akita mice treated with vehicle (n = 6) or TPTD (n = 7). TPTD or vehicle was administered subcutaneously 3 times a week for 8 weeks. Blood glucose, serum sclerostin, total tibial BMD, femoral shaft bone strength, and bone quality using Fourier-transform infrared spectroscopy imaging were evaluated. RESULTS: No significant differences in serum sclerostin levels were evident among these groups after 8 weeks of treatment. TPTD significantly increased BMD in control mice (+12.7%, P = 0.02) and Akita mice (+29.2%, P = 0.001) compared with vehicle. Maximum load and stiffness were significantly higher in Akita mice treated with TPTD than in Akita mice treated with vehicle (+56.6%, P = 0.03 and + 90.5%, P = 0.02, respectively). On Fourier-transform infrared spectroscopy imaging, the mineral/matrix ratio was significantly lower in Akita mice treated with vehicle than in control mice (−12.2%, P = 0.02), and TPTD treatment significantly increased the mineral/matrix ratio (P = 0.003). CONCLUSIONS: TPTD thus improved BMD and bone strength in both control mice and Akita mice, with improvements in the mineral/matrix ratio among Akita mice. Korean Society of Osteoporosis 2019-12 2019-12-10 /pmc/articles/PMC6953529/ /pubmed/31938729 http://dx.doi.org/10.1016/j.afos.2019.11.003 Text en © 2019 The Korean Society of Osteoporosis. Publishing services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Ohuchi, Kentaro Miyakoshi, Naohisa Kasukawa, Yuji Segawa, Toyohito Kinoshita, Hayato Sato, Chie Fujii, Masashi Shimada, Yoichi Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice) |
title | Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice) |
title_full | Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice) |
title_fullStr | Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice) |
title_full_unstemmed | Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice) |
title_short | Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice) |
title_sort | effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (akita mice) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953529/ https://www.ncbi.nlm.nih.gov/pubmed/31938729 http://dx.doi.org/10.1016/j.afos.2019.11.003 |
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