The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis

<p>Abstract</p> <p>Background</p> <p>We conducted the present study to investigate the therapeutic effects of a combination treatment of alfacalcidol (ALF) and risedronate (RIS) on the bone mechanical properties of bone and calcium (Ca) metabolism using an ovariectomize...

Full description

Bibliographic Details
Main Authors: Ito Masako, Umakoshi Yukichi, Nakano Takayoshi, Miyabe Sayaka, Shiraishi Ayako, Mihara Masahiko
Format: Article
Language:English
Published: BMC 2009-06-01
Series:BMC Musculoskeletal Disorders
Online Access:http://www.biomedcentral.com/1471-2474/10/66
_version_ 1819122778238877696
author Ito Masako
Umakoshi Yukichi
Nakano Takayoshi
Miyabe Sayaka
Shiraishi Ayako
Mihara Masahiko
author_facet Ito Masako
Umakoshi Yukichi
Nakano Takayoshi
Miyabe Sayaka
Shiraishi Ayako
Mihara Masahiko
author_sort Ito Masako
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>We conducted the present study to investigate the therapeutic effects of a combination treatment of alfacalcidol (ALF) and risedronate (RIS) on the bone mechanical properties of bone and calcium (Ca) metabolism using an ovariectomized (OVX) rat model of osteoporosis.</p> <p>Methods</p> <p>Female Wistar rats were OVX- or sham-operated at 40 weeks of age. Twelve weeks post-surgery, rats were randomized into seven groups: 1) sham + vehicle, 2) OVX + vehicle, 3) OVX + ALF 0.025 μg/kg/day, 4) OVX + ALF 0.05 μg, 5) OVX + RIS 0.3 mg, 6) OVX + RIS 3.0 mg, 7) OVX + ALF 0.025 μg + RIS 0.3 mg. Each drug was administered orally five times a week for 12 weeks. After treatment, we evaluated the mechanical properties of the lumbar vertebra and femoral midshaft. In the lumbar vertebra, structural and material analyses were performed using micro-computed tomography (micro-CT) and microbeam X-ray diffraction (micro-XRD), respectively. Biochemical markers in serum and urine were also determined.</p> <p>Results</p> <p>(1) With respect to improvement in the mechanical strength of the lumbar spine and the femoral midshaft, the combination treatment of ALF and RIS at their sub-therapeutic doses was more effective than each administered as a monotherapy; (2) In the suppression of bone resorption and the amelioration of microstructural parameters, the effects of ALF and RIS were considered to be independent and additive; (3) The improvement of material properties, such as microstructural parameters and the biological apatite (Bap) c-axis orientation, contributed to the reinforcement of spinal strength; and (4) The combination treatment of ALF and RIS normalized urinary Ca excretion, suggesting that this treatment ameliorated the changes in Ca metabolism.</p> <p>Conclusion</p> <p>These results demonstrate that the combination treatment of ALF and RIS at their sub-therapeutic doses can improve the mechanical properties of the spine as well as the femur and ameliorate changes in Ca metabolism in an animal model of osteoporosis, suggesting that the combination treatment of ALF and RIS has a therapeutic advantage over each monotherapy for the treatment of osteoporosis.</p>
first_indexed 2024-12-22T06:57:51Z
format Article
id doaj.art-4f087942efaf49a69b78dba884997ec6
institution Directory Open Access Journal
issn 1471-2474
language English
last_indexed 2024-12-22T06:57:51Z
publishDate 2009-06-01
publisher BMC
record_format Article
series BMC Musculoskeletal Disorders
spelling doaj.art-4f087942efaf49a69b78dba884997ec62022-12-21T18:34:53ZengBMCBMC Musculoskeletal Disorders1471-24742009-06-011016610.1186/1471-2474-10-66The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosisIto MasakoUmakoshi YukichiNakano TakayoshiMiyabe SayakaShiraishi AyakoMihara Masahiko<p>Abstract</p> <p>Background</p> <p>We conducted the present study to investigate the therapeutic effects of a combination treatment of alfacalcidol (ALF) and risedronate (RIS) on the bone mechanical properties of bone and calcium (Ca) metabolism using an ovariectomized (OVX) rat model of osteoporosis.</p> <p>Methods</p> <p>Female Wistar rats were OVX- or sham-operated at 40 weeks of age. Twelve weeks post-surgery, rats were randomized into seven groups: 1) sham + vehicle, 2) OVX + vehicle, 3) OVX + ALF 0.025 μg/kg/day, 4) OVX + ALF 0.05 μg, 5) OVX + RIS 0.3 mg, 6) OVX + RIS 3.0 mg, 7) OVX + ALF 0.025 μg + RIS 0.3 mg. Each drug was administered orally five times a week for 12 weeks. After treatment, we evaluated the mechanical properties of the lumbar vertebra and femoral midshaft. In the lumbar vertebra, structural and material analyses were performed using micro-computed tomography (micro-CT) and microbeam X-ray diffraction (micro-XRD), respectively. Biochemical markers in serum and urine were also determined.</p> <p>Results</p> <p>(1) With respect to improvement in the mechanical strength of the lumbar spine and the femoral midshaft, the combination treatment of ALF and RIS at their sub-therapeutic doses was more effective than each administered as a monotherapy; (2) In the suppression of bone resorption and the amelioration of microstructural parameters, the effects of ALF and RIS were considered to be independent and additive; (3) The improvement of material properties, such as microstructural parameters and the biological apatite (Bap) c-axis orientation, contributed to the reinforcement of spinal strength; and (4) The combination treatment of ALF and RIS normalized urinary Ca excretion, suggesting that this treatment ameliorated the changes in Ca metabolism.</p> <p>Conclusion</p> <p>These results demonstrate that the combination treatment of ALF and RIS at their sub-therapeutic doses can improve the mechanical properties of the spine as well as the femur and ameliorate changes in Ca metabolism in an animal model of osteoporosis, suggesting that the combination treatment of ALF and RIS has a therapeutic advantage over each monotherapy for the treatment of osteoporosis.</p>http://www.biomedcentral.com/1471-2474/10/66
spellingShingle Ito Masako
Umakoshi Yukichi
Nakano Takayoshi
Miyabe Sayaka
Shiraishi Ayako
Mihara Masahiko
The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis
BMC Musculoskeletal Disorders
title The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis
title_full The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis
title_fullStr The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis
title_full_unstemmed The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis
title_short The combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis
title_sort combination therapy with alfacalcidol and risedronate improves the mechanical property in lumbar spine by affecting the material properties in an ovariectomized rat model of osteoporosis
url http://www.biomedcentral.com/1471-2474/10/66
work_keys_str_mv AT itomasako thecombinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT umakoshiyukichi thecombinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT nakanotakayoshi thecombinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT miyabesayaka thecombinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT shiraishiayako thecombinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT miharamasahiko thecombinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT itomasako combinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT umakoshiyukichi combinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT nakanotakayoshi combinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT miyabesayaka combinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT shiraishiayako combinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis
AT miharamasahiko combinationtherapywithalfacalcidolandrisedronateimprovesthemechanicalpropertyinlumbarspinebyaffectingthematerialpropertiesinanovariectomizedratmodelofosteoporosis