Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas

Detalhes bibliográficos
Autor(a) principal: Pimentel, Fernanda Scarpatti
Data de Publicação: 2010
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
Texto Completo: http://repositorio.ufes.br/handle/10/5750
Resumo: The bone is a specialized form of connective tissue that provides support for metabolic and biomechanical throughout the body. Thus, the bone is very dynamic, with constantly renewing itself. His integrity therefore depends on the balance between the processes of formation and resorption. The loss of this balance alters both the structure of organic matrix as bone mineralization. Moreover, imbalances in bone remodeling process may result in the development of systemic skeletal diseases such as osteoporosis. The osteoporosis is a chronic progressive disease that affects millions of people around the world. Only in Brazil some 10 million people suffer from osteoporosis. The hormone estrogen deficiency induced by ovariectomy (OVX) rats, demonstrably stimulates increased bone resorption, especially in long bones and spine, mimicking what happens in postmenopausal osteoporosis. In this work we used OVX rats to investigate the interaction of alendronate (a drug widely used to treat osteoporosis) and vitamin K (VK) (recent investigations have pointed anabolic bone tissue of osteoporotic patients) in the metabolism osteomineral. This study revealed that administration of alendronate (ALE) and VK with ALE (ALE+VK) produced significant recovery in bone mineral density (BMD) in OVX rats. However, the use of VK alone did not appear to make any significant effect on BMD in OVX rats. We observed an increased excretion of urinary deoxypyridinoline (DPD), a marker of bone resorption, in OVX group, and statistically significant reduction of DPD when the animals were treated with VK, ALE, or both. There was no statistically significant difference in bone mineral content and body surface area. Was verified statistically significant difference in the thickness of compact bone in the different study groups. There was also a statistically significant reduction in wet weight and endometrium of OVX rats, demonstrating the effectiveness of ovariectomy. Therefore, the animal model used in this study efficiently mimicked estrogen deficiency induced by ovariectomy, resulting in increased bone resorption; treatment with ALE and VK+ALE increases BMD in OVX rats, while the VK alone does not produce this effect; treatment with ALE and VK reduces bone resorption in OVX rats, verified by the reduction in the excretion of DPD
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spelling Rangel, Leticia Batista AzevedoSilva, Ian VictorPimentel, Fernanda ScarpattiBissoli, Nazaré SouzaMiranda, Kildare Rocha de2016-12-23T13:49:04Z2011-04-152016-12-23T13:49:04Z2010-07-29The bone is a specialized form of connective tissue that provides support for metabolic and biomechanical throughout the body. Thus, the bone is very dynamic, with constantly renewing itself. His integrity therefore depends on the balance between the processes of formation and resorption. The loss of this balance alters both the structure of organic matrix as bone mineralization. Moreover, imbalances in bone remodeling process may result in the development of systemic skeletal diseases such as osteoporosis. The osteoporosis is a chronic progressive disease that affects millions of people around the world. Only in Brazil some 10 million people suffer from osteoporosis. The hormone estrogen deficiency induced by ovariectomy (OVX) rats, demonstrably stimulates increased bone resorption, especially in long bones and spine, mimicking what happens in postmenopausal osteoporosis. In this work we used OVX rats to investigate the interaction of alendronate (a drug widely used to treat osteoporosis) and vitamin K (VK) (recent investigations have pointed anabolic bone tissue of osteoporotic patients) in the metabolism osteomineral. This study revealed that administration of alendronate (ALE) and VK with ALE (ALE+VK) produced significant recovery in bone mineral density (BMD) in OVX rats. However, the use of VK alone did not appear to make any significant effect on BMD in OVX rats. We observed an increased excretion of urinary deoxypyridinoline (DPD), a marker of bone resorption, in OVX group, and statistically significant reduction of DPD when the animals were treated with VK, ALE, or both. There was no statistically significant difference in bone mineral content and body surface area. Was verified statistically significant difference in the thickness of compact bone in the different study groups. There was also a statistically significant reduction in wet weight and endometrium of OVX rats, demonstrating the effectiveness of ovariectomy. Therefore, the animal model used in this study efficiently mimicked estrogen deficiency induced by ovariectomy, resulting in increased bone resorption; treatment with ALE and VK+ALE increases BMD in OVX rats, while the VK alone does not produce this effect; treatment with ALE and VK reduces bone resorption in OVX rats, verified by the reduction in the excretion of DPDO osso é uma forma especializada de tecido conjuntivo que fornece suporte biomecânico e metabólico para todo o corpo. Para tanto, o tecido ósseo é muito dinâmico, apresentando-se em constante renovação. Sua integridade depende, portanto, do equilíbrio entre os processos de formação e reabsorção óssea. Ademais, desequilíbrios no processo de remodelamento ósseo podem resultar no desenvolvimento de doenças esqueléticas sistêmicas, como a osteoporose. A osteoporose é uma doença crônica e progressiva que afeta milhões de pessoas em todo o mundo. Somente no Brasil cerca de 10 milhões de pessoas sofrem de osteoporose. A deficiência hormonal estrogênica, induzida pela ovariectomia (OVX) em ratos, comprovadamente estimula o aumento da reabsorção óssea, principalmente em ossos longos e coluna vertebral, mimetizando o que acontece na osteoporose pós-menopausa. No presente trabalho foram utilizadas ratas OVX para se investigar a interação do alendronato (fármaco extensamente utilizado no tratamento da osteoporose) e da vitamina K (VK) (recentes investigações apontam possuir ação anabólica do tecido ósseo de pacientes osteoporóticas) no metabolismo osteomineral. Este estudo revelou que a administração de alendronato (ALE) e de VK juntamente com ALE (VK+ALE) produziu significante recuperação na densidade mineral óssea (DMO) de ratas OVX. No entanto, a utilização da VK isoladamente não pareceu exercer nenhum efeito significante na DMO de ratas OVX. Observou-se uma maior excreção de deoxipiridinolinas urinárias (DPD), marcador de reabsorção óssea no grupo OVX, e redução estatisticamente significante da DPD quando os animais foram tratados com VK, ALE ou ambas. Não houve diferença estatisticamente significante do conteúdo mineral ósseo e da área corporal. Também não foi verificada diferença estatisticamente significante na espessura do osso compacto nos diferentes grupos de estudo. Verificou-se ainda redução estatisticamente significante do peso úmido e do endométrio de ratas OVX, comprovando a eficiência da ovariectomia. Portanto, o modelo animal utilizado neste estudo mimetizou eficientemente a deficiência estrogênica induzida pela ovariectomia, resultando em aumento da reabsorção óssea; o tratamento com ALE e VK+ALE aumenta a DMO de ratas OVX, embora a VK isoladamente não apresente esse efeito; o tratamento com ALE e VK reduz a reabsorção óssea de ratas OVX, verificada pela redução na excreção de DPDTextPIMENTEL, Fernanda Scarpatti. Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas. 2010. 92 f. Dissertação (Mestrado em Biotecnologia) - Programa de Pós-Graduação em Biotecnologia, Universidade Federal do Espírito Santo, Vitória, 2010.http://repositorio.ufes.br/handle/10/5750porUniversidade Federal do Espírito SantoMestrado em BiotecnologiaPrograma de Pós-Graduação em BiotecnologiaUFESBRCentro de Ciências da SaúdeBoneRemodelingOsteoporosisPostmenopausalAlendronateVitamin KOssoRemodelamentoOsteoporosePós-menopausaAlendronatoVitamina KBiotecnologia61Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadasinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)instname:Universidade Federal do Espírito Santo (UFES)instacron:UFESORIGINALDissertacao de Fernanda Scarpatti Pimentel.pdfapplication/pdf2000878http://repositorio.ufes.br/bitstreams/26d697d8-d284-49ef-8cf6-aa7857a7249a/downloadcdfb57d1ceb94c6e6c0b410060dcfbfbMD5110/57502024-07-16 17:06:33.167oai:repositorio.ufes.br:10/5750http://repositorio.ufes.brRepositório InstitucionalPUBhttp://repositorio.ufes.br/oai/requestopendoar:21082024-10-15T17:56:15.808211Repositório Institucional da Universidade Federal do Espírito Santo (riUfes) - Universidade Federal do Espírito Santo (UFES)false
dc.title.none.fl_str_mv Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
title Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
spellingShingle Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
Pimentel, Fernanda Scarpatti
Bone
Remodeling
Osteoporosis
Postmenopausal
Alendronate
Vitamin K
Osso
Remodelamento
Osteoporose
Pós-menopausa
Alendronato
Vitamina K
Biotecnologia
61
title_short Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
title_full Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
title_fullStr Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
title_full_unstemmed Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
title_sort Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas
author Pimentel, Fernanda Scarpatti
author_facet Pimentel, Fernanda Scarpatti
author_role author
dc.contributor.advisor-co1.fl_str_mv Rangel, Leticia Batista Azevedo
dc.contributor.advisor1.fl_str_mv Silva, Ian Victor
dc.contributor.author.fl_str_mv Pimentel, Fernanda Scarpatti
dc.contributor.referee1.fl_str_mv Bissoli, Nazaré Souza
dc.contributor.referee2.fl_str_mv Miranda, Kildare Rocha de
contributor_str_mv Rangel, Leticia Batista Azevedo
Silva, Ian Victor
Bissoli, Nazaré Souza
Miranda, Kildare Rocha de
dc.subject.eng.fl_str_mv Bone
Remodeling
Osteoporosis
Postmenopausal
Alendronate
Vitamin K
topic Bone
Remodeling
Osteoporosis
Postmenopausal
Alendronate
Vitamin K
Osso
Remodelamento
Osteoporose
Pós-menopausa
Alendronato
Vitamina K
Biotecnologia
61
dc.subject.por.fl_str_mv Osso
Remodelamento
Osteoporose
Pós-menopausa
Alendronato
Vitamina K
dc.subject.cnpq.fl_str_mv Biotecnologia
dc.subject.udc.none.fl_str_mv 61
description The bone is a specialized form of connective tissue that provides support for metabolic and biomechanical throughout the body. Thus, the bone is very dynamic, with constantly renewing itself. His integrity therefore depends on the balance between the processes of formation and resorption. The loss of this balance alters both the structure of organic matrix as bone mineralization. Moreover, imbalances in bone remodeling process may result in the development of systemic skeletal diseases such as osteoporosis. The osteoporosis is a chronic progressive disease that affects millions of people around the world. Only in Brazil some 10 million people suffer from osteoporosis. The hormone estrogen deficiency induced by ovariectomy (OVX) rats, demonstrably stimulates increased bone resorption, especially in long bones and spine, mimicking what happens in postmenopausal osteoporosis. In this work we used OVX rats to investigate the interaction of alendronate (a drug widely used to treat osteoporosis) and vitamin K (VK) (recent investigations have pointed anabolic bone tissue of osteoporotic patients) in the metabolism osteomineral. This study revealed that administration of alendronate (ALE) and VK with ALE (ALE+VK) produced significant recovery in bone mineral density (BMD) in OVX rats. However, the use of VK alone did not appear to make any significant effect on BMD in OVX rats. We observed an increased excretion of urinary deoxypyridinoline (DPD), a marker of bone resorption, in OVX group, and statistically significant reduction of DPD when the animals were treated with VK, ALE, or both. There was no statistically significant difference in bone mineral content and body surface area. Was verified statistically significant difference in the thickness of compact bone in the different study groups. There was also a statistically significant reduction in wet weight and endometrium of OVX rats, demonstrating the effectiveness of ovariectomy. Therefore, the animal model used in this study efficiently mimicked estrogen deficiency induced by ovariectomy, resulting in increased bone resorption; treatment with ALE and VK+ALE increases BMD in OVX rats, while the VK alone does not produce this effect; treatment with ALE and VK reduces bone resorption in OVX rats, verified by the reduction in the excretion of DPD
publishDate 2010
dc.date.issued.fl_str_mv 2010-07-29
dc.date.available.fl_str_mv 2011-04-15
2016-12-23T13:49:04Z
dc.date.accessioned.fl_str_mv 2016-12-23T13:49:04Z
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dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.identifier.citation.fl_str_mv PIMENTEL, Fernanda Scarpatti. Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas. 2010. 92 f. Dissertação (Mestrado em Biotecnologia) - Programa de Pós-Graduação em Biotecnologia, Universidade Federal do Espírito Santo, Vitória, 2010.
dc.identifier.uri.fl_str_mv http://repositorio.ufes.br/handle/10/5750
identifier_str_mv PIMENTEL, Fernanda Scarpatti. Interação do alendronato e da vitamina K no metabolismo osteomineral de ratas ovariectomizadas. 2010. 92 f. Dissertação (Mestrado em Biotecnologia) - Programa de Pós-Graduação em Biotecnologia, Universidade Federal do Espírito Santo, Vitória, 2010.
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publisher.none.fl_str_mv Universidade Federal do Espírito Santo
Mestrado em Biotecnologia
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