Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats

Detalhes bibliográficos
Autor(a) principal: Pereira,F.A.
Data de Publicação: 2012
Outros Autores: Mattar,R., Facincani,I., Defino,H.L.A., Ramalho,L.N.Z., Jorgetti,V., Volpon,J.B., Paula,F.J.A. de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Medical and Biological Research
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012001200021
Resumo: Osteoporosis is a major complication of chronic cholestatic liver disease (CCLD). We evaluated the efficacy of using disodium pamidronate (1.0 mg/kg body weight) for the prevention (Pr) or treatment (Tr) of cholestasis-induced osteoporosis in male Wistar rats: sham-operated (Sham = 12); bile duct-ligated (Bi = 15); bile duct-ligated animals previously treated with pamidronate before and 1 month after surgery (Pr = 9); bile duct-ligated animals treated with pamidronate 1 month after surgery (Tr = 9). Rats were sacrificed 8 weeks after surgery. Immunohistochemical expression of IGF-I and GH receptor was determined in the proximal growth plate cartilage of the left tibia. Histomorphometric analysis was performed in the right tibia and the right femur was used for biomechanical analysis. Bone material volume over tissue volume (BV/TV) was significantly affected by CCLD (Sham = 18.1 ± 3.2 vs Bi = 10.6 ± 2.2%) and pamidronate successfully increased bone volume. However, pamidronate administered in a preventive regimen presented no additional benefit on bone volume compared to secondary treatment (BV/TV: Pr = 39.4 ± 12.0; Tr = 41.2 ± 12.7%). Moreover, the force on the momentum of fracture was significantly reduced in Pr rats (Sham = 116.6 ± 23.0; Bi = 94.6 ± 33.8; Pr = 82.9 ± 22.8; Tr = 92.5 ± 29.5 N; P < 0.05, Sham vs Pr). Thus, CCLD had a significant impact on bone histomorphometric parameters and pamidronate was highly effective in increasing bone mass in CCLD; however, preventive therapy with pamidronate has no advantage regarding bone fragility.
id ABDC-1_9588655127ce62f505d97a3534440b9e
oai_identifier_str oai:scielo:S0100-879X2012001200021
network_acronym_str ABDC-1
network_name_str Brazilian Journal of Medical and Biological Research
repository_id_str
spelling Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar ratsHepatic osteodystrophyOsteoporosis pathogenesisGrowth factorsBiomechanicsAnimal modelsPamidronateOsteoporosis is a major complication of chronic cholestatic liver disease (CCLD). We evaluated the efficacy of using disodium pamidronate (1.0 mg/kg body weight) for the prevention (Pr) or treatment (Tr) of cholestasis-induced osteoporosis in male Wistar rats: sham-operated (Sham = 12); bile duct-ligated (Bi = 15); bile duct-ligated animals previously treated with pamidronate before and 1 month after surgery (Pr = 9); bile duct-ligated animals treated with pamidronate 1 month after surgery (Tr = 9). Rats were sacrificed 8 weeks after surgery. Immunohistochemical expression of IGF-I and GH receptor was determined in the proximal growth plate cartilage of the left tibia. Histomorphometric analysis was performed in the right tibia and the right femur was used for biomechanical analysis. Bone material volume over tissue volume (BV/TV) was significantly affected by CCLD (Sham = 18.1 ± 3.2 vs Bi = 10.6 ± 2.2%) and pamidronate successfully increased bone volume. However, pamidronate administered in a preventive regimen presented no additional benefit on bone volume compared to secondary treatment (BV/TV: Pr = 39.4 ± 12.0; Tr = 41.2 ± 12.7%). Moreover, the force on the momentum of fracture was significantly reduced in Pr rats (Sham = 116.6 ± 23.0; Bi = 94.6 ± 33.8; Pr = 82.9 ± 22.8; Tr = 92.5 ± 29.5 N; P < 0.05, Sham vs Pr). Thus, CCLD had a significant impact on bone histomorphometric parameters and pamidronate was highly effective in increasing bone mass in CCLD; however, preventive therapy with pamidronate has no advantage regarding bone fragility.Associação Brasileira de Divulgação Científica2012-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012001200021Brazilian Journal of Medical and Biological Research v.45 n.12 2012reponame:Brazilian Journal of Medical and Biological Researchinstname:Associação Brasileira de Divulgação Científica (ABDC)instacron:ABDC10.1590/S0100-879X2012007500143info:eu-repo/semantics/openAccessPereira,F.A.Mattar,R.Facincani,I.Defino,H.L.A.Ramalho,L.N.Z.Jorgetti,V.Volpon,J.B.Paula,F.J.A. deeng2012-12-14T00:00:00Zoai:scielo:S0100-879X2012001200021Revistahttps://www.bjournal.org/https://old.scielo.br/oai/scielo-oai.phpbjournal@terra.com.br||bjournal@terra.com.br1414-431X0100-879Xopendoar:2012-12-14T00:00Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)false
dc.title.none.fl_str_mv Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
title Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
spellingShingle Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
Pereira,F.A.
Hepatic osteodystrophy
Osteoporosis pathogenesis
Growth factors
Biomechanics
Animal models
Pamidronate
title_short Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
title_full Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
title_fullStr Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
title_full_unstemmed Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
title_sort Pamidronate for the treatment of osteoporosis secondary to chronic cholestatic liver disease in Wistar rats
author Pereira,F.A.
author_facet Pereira,F.A.
Mattar,R.
Facincani,I.
Defino,H.L.A.
Ramalho,L.N.Z.
Jorgetti,V.
Volpon,J.B.
Paula,F.J.A. de
author_role author
author2 Mattar,R.
Facincani,I.
Defino,H.L.A.
Ramalho,L.N.Z.
Jorgetti,V.
Volpon,J.B.
Paula,F.J.A. de
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pereira,F.A.
Mattar,R.
Facincani,I.
Defino,H.L.A.
Ramalho,L.N.Z.
Jorgetti,V.
Volpon,J.B.
Paula,F.J.A. de
dc.subject.por.fl_str_mv Hepatic osteodystrophy
Osteoporosis pathogenesis
Growth factors
Biomechanics
Animal models
Pamidronate
topic Hepatic osteodystrophy
Osteoporosis pathogenesis
Growth factors
Biomechanics
Animal models
Pamidronate
description Osteoporosis is a major complication of chronic cholestatic liver disease (CCLD). We evaluated the efficacy of using disodium pamidronate (1.0 mg/kg body weight) for the prevention (Pr) or treatment (Tr) of cholestasis-induced osteoporosis in male Wistar rats: sham-operated (Sham = 12); bile duct-ligated (Bi = 15); bile duct-ligated animals previously treated with pamidronate before and 1 month after surgery (Pr = 9); bile duct-ligated animals treated with pamidronate 1 month after surgery (Tr = 9). Rats were sacrificed 8 weeks after surgery. Immunohistochemical expression of IGF-I and GH receptor was determined in the proximal growth plate cartilage of the left tibia. Histomorphometric analysis was performed in the right tibia and the right femur was used for biomechanical analysis. Bone material volume over tissue volume (BV/TV) was significantly affected by CCLD (Sham = 18.1 ± 3.2 vs Bi = 10.6 ± 2.2%) and pamidronate successfully increased bone volume. However, pamidronate administered in a preventive regimen presented no additional benefit on bone volume compared to secondary treatment (BV/TV: Pr = 39.4 ± 12.0; Tr = 41.2 ± 12.7%). Moreover, the force on the momentum of fracture was significantly reduced in Pr rats (Sham = 116.6 ± 23.0; Bi = 94.6 ± 33.8; Pr = 82.9 ± 22.8; Tr = 92.5 ± 29.5 N; P < 0.05, Sham vs Pr). Thus, CCLD had a significant impact on bone histomorphometric parameters and pamidronate was highly effective in increasing bone mass in CCLD; however, preventive therapy with pamidronate has no advantage regarding bone fragility.
publishDate 2012
dc.date.none.fl_str_mv 2012-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012001200021
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012001200021
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0100-879X2012007500143
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
dc.source.none.fl_str_mv Brazilian Journal of Medical and Biological Research v.45 n.12 2012
reponame:Brazilian Journal of Medical and Biological Research
instname:Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
instname_str Associação Brasileira de Divulgação Científica (ABDC)
instacron_str ABDC
institution ABDC
reponame_str Brazilian Journal of Medical and Biological Research
collection Brazilian Journal of Medical and Biological Research
repository.name.fl_str_mv Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)
repository.mail.fl_str_mv bjournal@terra.com.br||bjournal@terra.com.br
_version_ 1754302941680893952