Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Manancial - Repositório Digital da UFSM |
dARK ID: | ark:/26339/0013000013tpr |
Texto Completo: | http://repositorio.ufsm.br/handle/1/4046 |
Resumo: | The difficulty to repair chondral lesions due to low mitotic activity, absence of vessels and blood supply, nerves and lack of support by the immobility of articular chondrocytes is a challenge for the orthopedist. Conventional and surgical alternatives usually result in relieving symptoms of the patient without, however, the formation of hyaline tissue at the injury site. Gene and cell therapy has been very promising as a treatment option. There is a great prospect for clinical use of modern technology, emerging as an alternative solution for the patient. This work aimed to develop a lesion in the trochlear groove articular cartilage of dogs using the technique of trochleoplasty widely used as a treatment of patellar dislocation in dogs. The study included 36 dogs, divided into three groups of 12 animals each with different treatments. For the control group 1arise grafting was not used, the group 2 was placed sponge collagen sponge (Gelfoam ®) and group 3 (cells) beyond the collagen sponge is added to the same total fraction of autologous mononuclear cells previously collected and processed in the laboratory. Each group was subdivided into groups of four animals that were differentiated by the follow-up period was 30, 60 and 90 days postoperatively. We evaluated clinical, radiologic, fluorescent, perimetry and histological and comparative analysis between the three groups. Animals with the addition of cells was better with clinically early support of the operated limb compared to other groups. Other evaluations were similar among all animals with no statistical differences but unlike previous studies signs of hyaline repair were found. It is concluded that the use of cell therapy accelerated the repair of cartilage injury with no difference in the quality of the final model. |
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Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cãesAdult autologous stem cell as ajuvants in repair of articular cartilage in dogs of experimental trochleoplastyCélulas mononuclearesMedula ósseaTrocleoplastiaCartilagemCãesMononuclear cellsBone marrowTrochleoplastyCartilageDogsCNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIAThe difficulty to repair chondral lesions due to low mitotic activity, absence of vessels and blood supply, nerves and lack of support by the immobility of articular chondrocytes is a challenge for the orthopedist. Conventional and surgical alternatives usually result in relieving symptoms of the patient without, however, the formation of hyaline tissue at the injury site. Gene and cell therapy has been very promising as a treatment option. There is a great prospect for clinical use of modern technology, emerging as an alternative solution for the patient. This work aimed to develop a lesion in the trochlear groove articular cartilage of dogs using the technique of trochleoplasty widely used as a treatment of patellar dislocation in dogs. The study included 36 dogs, divided into three groups of 12 animals each with different treatments. For the control group 1arise grafting was not used, the group 2 was placed sponge collagen sponge (Gelfoam ®) and group 3 (cells) beyond the collagen sponge is added to the same total fraction of autologous mononuclear cells previously collected and processed in the laboratory. Each group was subdivided into groups of four animals that were differentiated by the follow-up period was 30, 60 and 90 days postoperatively. We evaluated clinical, radiologic, fluorescent, perimetry and histological and comparative analysis between the three groups. Animals with the addition of cells was better with clinically early support of the operated limb compared to other groups. Other evaluations were similar among all animals with no statistical differences but unlike previous studies signs of hyaline repair were found. It is concluded that the use of cell therapy accelerated the repair of cartilage injury with no difference in the quality of the final model.A dificuldade de reparo de lesões condrais, devido a baixa atividade mitótica, pela ausência de vasos e irrigação sanguinea, ausência de suporte nervoso e pela imobilidade dos condrócitos articulares é um desafio para os ortopedistas. Alternativas convencionais e cirúrgicas normalmente resultam em alívio de sintomas do paciente sem, no entanto, a formação de tecido hialino no local da lesão. A terapia celular e gênica tem-se mostrado muito promissora como opção de tratamento. Há uma grande perspectiva de uso clínico desta moderna tecnologia, surgindo como alternativa de solução para o paciente. Este trabalho constituiu em desenvolver lesão em cartilagem articular no sulco troclear de cães através da técnica de trocleoplastia muito utilizada como tratamento de luxação de patela de cães. Foram utilizados 36 cães, divididos em 3 grupos de 12 animais com tratamentos diferentes. No grupo 1 (controle) não se colocava enxertia, no grupo 2 (esponja) se colocava esponja de colágeno (Gelfoam®) e no grupo 3 (células) além da esponja de colágeno se adicionava a mesma a fração total de células mononucleares autógenas previamente colhidas e processadas em laboratório. Cada grupo foi subdividido em grupos de 4 animais que se diferenciavam pelo período de acompanhamento que foi de 30, 60 e 90 dias de pós-operatório. Foram realizadas avaliações clínicas, radiológicas, fluorescentes, perimetrias e histológicas e análises comparativas entre os três grupos estudados. Os animais com adição de células se mostrou superior clinicamente com apoio precoce do membro operado em relação aos demais grupos. As demais avaliações se mostraram semelhantes entre todos os animais sem diferenças estatísticas mas diferentemente dos estudos anteriores se encontrou sinais de reparação hialina. Concluindo assim que o uso de terapia celular acelerou o processo de reparação em lesão cartilaginosa sem diferença na qualidade do tecido final do modelo proposto.Universidade Federal de Santa MariaBRMedicina VeterináriaUFSMPrograma de Pós-Graduação em Medicina VeterináriaMazzanti, Alexandrehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4795593E6Silva Filho, Antonio de Pádua Ferreira dahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4780750A1Graça, Dominguita Luhershttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4783904A3Contesini, Emerson Antoniohttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4784012D5Aguiar, Eduardo Santiago Ventura dehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4761469D6Santos Junior, Eduardo de Bastos2017-06-012017-06-012010-06-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfapplication/pdfSANTOS JUNIOR, Eduardo de Bastos. Adult autologous stem cell as ajuvants in repair of articular cartilage in dogs of experimental trochleoplasty. 2010. 151 f. Tese (Doutorado em Medicina Veterinária) - Universidade Federal de Santa Maria, Santa Maria, 2010.http://repositorio.ufsm.br/handle/1/4046ark:/26339/0013000013tprporinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2017-07-25T14:03:22Zoai:repositorio.ufsm.br:1/4046Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2017-07-25T14:03:22Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false |
dc.title.none.fl_str_mv |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães Adult autologous stem cell as ajuvants in repair of articular cartilage in dogs of experimental trochleoplasty |
title |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães |
spellingShingle |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães Santos Junior, Eduardo de Bastos Células mononucleares Medula óssea Trocleoplastia Cartilagem Cães Mononuclear cells Bone marrow Trochleoplasty Cartilage Dogs CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA |
title_short |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães |
title_full |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães |
title_fullStr |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães |
title_full_unstemmed |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães |
title_sort |
Fração total de células mononucleares como adjuvantes no reparo de cartilagem articular em trocleoplastia experimental de cães |
author |
Santos Junior, Eduardo de Bastos |
author_facet |
Santos Junior, Eduardo de Bastos |
author_role |
author |
dc.contributor.none.fl_str_mv |
Mazzanti, Alexandre http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4795593E6 Silva Filho, Antonio de Pádua Ferreira da http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4780750A1 Graça, Dominguita Luhers http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4783904A3 Contesini, Emerson Antonio http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4784012D5 Aguiar, Eduardo Santiago Ventura de http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4761469D6 |
dc.contributor.author.fl_str_mv |
Santos Junior, Eduardo de Bastos |
dc.subject.por.fl_str_mv |
Células mononucleares Medula óssea Trocleoplastia Cartilagem Cães Mononuclear cells Bone marrow Trochleoplasty Cartilage Dogs CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA |
topic |
Células mononucleares Medula óssea Trocleoplastia Cartilagem Cães Mononuclear cells Bone marrow Trochleoplasty Cartilage Dogs CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA |
description |
The difficulty to repair chondral lesions due to low mitotic activity, absence of vessels and blood supply, nerves and lack of support by the immobility of articular chondrocytes is a challenge for the orthopedist. Conventional and surgical alternatives usually result in relieving symptoms of the patient without, however, the formation of hyaline tissue at the injury site. Gene and cell therapy has been very promising as a treatment option. There is a great prospect for clinical use of modern technology, emerging as an alternative solution for the patient. This work aimed to develop a lesion in the trochlear groove articular cartilage of dogs using the technique of trochleoplasty widely used as a treatment of patellar dislocation in dogs. The study included 36 dogs, divided into three groups of 12 animals each with different treatments. For the control group 1arise grafting was not used, the group 2 was placed sponge collagen sponge (Gelfoam ®) and group 3 (cells) beyond the collagen sponge is added to the same total fraction of autologous mononuclear cells previously collected and processed in the laboratory. Each group was subdivided into groups of four animals that were differentiated by the follow-up period was 30, 60 and 90 days postoperatively. We evaluated clinical, radiologic, fluorescent, perimetry and histological and comparative analysis between the three groups. Animals with the addition of cells was better with clinically early support of the operated limb compared to other groups. Other evaluations were similar among all animals with no statistical differences but unlike previous studies signs of hyaline repair were found. It is concluded that the use of cell therapy accelerated the repair of cartilage injury with no difference in the quality of the final model. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-06-11 2017-06-01 2017-06-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/doctoralThesis |
format |
doctoralThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
SANTOS JUNIOR, Eduardo de Bastos. Adult autologous stem cell as ajuvants in repair of articular cartilage in dogs of experimental trochleoplasty. 2010. 151 f. Tese (Doutorado em Medicina Veterinária) - Universidade Federal de Santa Maria, Santa Maria, 2010. http://repositorio.ufsm.br/handle/1/4046 |
dc.identifier.dark.fl_str_mv |
ark:/26339/0013000013tpr |
identifier_str_mv |
SANTOS JUNIOR, Eduardo de Bastos. Adult autologous stem cell as ajuvants in repair of articular cartilage in dogs of experimental trochleoplasty. 2010. 151 f. Tese (Doutorado em Medicina Veterinária) - Universidade Federal de Santa Maria, Santa Maria, 2010. ark:/26339/0013000013tpr |
url |
http://repositorio.ufsm.br/handle/1/4046 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Santa Maria BR Medicina Veterinária UFSM Programa de Pós-Graduação em Medicina Veterinária |
publisher.none.fl_str_mv |
Universidade Federal de Santa Maria BR Medicina Veterinária UFSM Programa de Pós-Graduação em Medicina Veterinária |
dc.source.none.fl_str_mv |
reponame:Manancial - Repositório Digital da UFSM instname:Universidade Federal de Santa Maria (UFSM) instacron:UFSM |
instname_str |
Universidade Federal de Santa Maria (UFSM) |
instacron_str |
UFSM |
institution |
UFSM |
reponame_str |
Manancial - Repositório Digital da UFSM |
collection |
Manancial - Repositório Digital da UFSM |
repository.name.fl_str_mv |
Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM) |
repository.mail.fl_str_mv |
atendimento.sib@ufsm.br||tedebc@gmail.com |
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1815172444051210240 |