Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1186/scrt236 http://hdl.handle.net/11449/76051 |
Resumo: | Introduction. Tendon injury is a major cause of lameness and decreased performance in athletic equines. Various therapies for tendonitis have been described; however, none of these therapies results in complete tissue regeneration, and the injury recurrence rate is high even after long recovery periods involving rest and physiotherapy. Methods. A lesion was induced with collagenase gel in the superficial digital flexor tendon in the center portion of the metacarpal region of eight equines of mixed breed. After two weeks, the lesions of the animals in the treated and control groups were treated through the intralesional administration of mesenchymal stem cells derived from adipose tissue (adMSCs) suspended in platelet concentrate (PC) and with phosphate buffered saline (PBS), respectively. Serial ultrasound analyses were performed every two weeks. After 16 weeks of therapy, a biopsy was performed for histopathological, immunohistochemical and gene expression (type I collagen (COL1A1), type III collagen (COL3A1), tenascin-C (TNC), tenomodulin (TNMD), and scleraxis (SCX)) analyses. Results: Differences in the ultrasound and histopathological analyses were observed between the groups. Improved results were reported in the group treated with adMSCs suspended in PC. There was no difference in the gene expression levels observed after the different treatments. The main results observed from the histopathological evaluation of the treated group were as follows: a prevention of the progression of the lesion, a greater organization of collagen fibers, and a decreased inflammatory infiltrate. A lack of progression of the lesion area and its percentage was observed in the ultrasound image, and increased blood flow was measured by Power Doppler. Conclusions: The use of adMSCs combined with PC for the therapy of experimentally induced tendonitis prevented the progression of the tendon lesion, as observed in the ultrasound examination, and resulted in a greater organization and decreased inflammation, as observed in the histopathological evaluation. These data demonstrate the therapeutic potential of this therapy for the treatment of equine tendonitis. © 2013 Carvalho et al.; licensee BioMed Central Ltd. |
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Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trialHorseStem cellTendon lesionTreatmentcollagen fibercollagen type 1membrane proteinphosphate buffered salinescleraxistenascintenomodulinunclassified drugadipose tissueanimal cellanimal experimentanimal tissueautologous stem cell transplantationblood flowcell isolationclinical evaluationCOL1A1 geneCOL3A1 genecontrolled studydigital flxeor tendon therapyDoppler flowmeterequine tendonitisfemalegenegene expressionhistopathologyhorse diseaseimage analysisimmunohistochemistryinflammatory infiltratemalemesenchymal stem cell transplantationnonhumanphysical activitypriority journalprophylaxisrandomized controlled trialSCX genetendinitistendonthrombocyte transfusiontnc geneTNMD genetreatment outcometreatment responseultrasoundAnimaliaEquidaeIntroduction. Tendon injury is a major cause of lameness and decreased performance in athletic equines. Various therapies for tendonitis have been described; however, none of these therapies results in complete tissue regeneration, and the injury recurrence rate is high even after long recovery periods involving rest and physiotherapy. Methods. A lesion was induced with collagenase gel in the superficial digital flexor tendon in the center portion of the metacarpal region of eight equines of mixed breed. After two weeks, the lesions of the animals in the treated and control groups were treated through the intralesional administration of mesenchymal stem cells derived from adipose tissue (adMSCs) suspended in platelet concentrate (PC) and with phosphate buffered saline (PBS), respectively. Serial ultrasound analyses were performed every two weeks. After 16 weeks of therapy, a biopsy was performed for histopathological, immunohistochemical and gene expression (type I collagen (COL1A1), type III collagen (COL3A1), tenascin-C (TNC), tenomodulin (TNMD), and scleraxis (SCX)) analyses. Results: Differences in the ultrasound and histopathological analyses were observed between the groups. Improved results were reported in the group treated with adMSCs suspended in PC. There was no difference in the gene expression levels observed after the different treatments. The main results observed from the histopathological evaluation of the treated group were as follows: a prevention of the progression of the lesion, a greater organization of collagen fibers, and a decreased inflammatory infiltrate. A lack of progression of the lesion area and its percentage was observed in the ultrasound image, and increased blood flow was measured by Power Doppler. Conclusions: The use of adMSCs combined with PC for the therapy of experimentally induced tendonitis prevented the progression of the tendon lesion, as observed in the ultrasound examination, and resulted in a greater organization and decreased inflammation, as observed in the histopathological evaluation. These data demonstrate the therapeutic potential of this therapy for the treatment of equine tendonitis. © 2013 Carvalho et al.; licensee BioMed Central Ltd.Department of Veterinary Surgery and Anesthesiology School of Veterinary Medicine and Animal Science São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloDepartment of Veterinary Clinic School of Veterinary Medicine and Animal Science São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloDepartment of Animal Reproduction and Veterinary Radiology School of Veterinary Medicine and Animal Science São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloBlood Center Botucatu Medical School São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloDepartment of Veterinary Surgery and Anesthesiology School of Veterinary Medicine and Animal Science São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloDepartment of Veterinary Clinic School of Veterinary Medicine and Animal Science São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloDepartment of Animal Reproduction and Veterinary Radiology School of Veterinary Medicine and Animal Science São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloBlood Center Botucatu Medical School São Paulo State University Rubião Junior, 18618-970 Botucatu, São PauloUniversidade Estadual Paulista (Unesp)Carvalho, Armando de Mattos [UNESP]Badial, Peres Ramos [UNESP]Álvarez, Luis Emiliano Cisneros [UNESP]Yamada, Ana Lucia Miluzzi [UNESP]Borges, Alexandre Secorun [UNESP]Deffune, Elenice [UNESP]Hussni, Carlos Alberto [UNESP]Alves, Ana Liz Garcia [UNESP]2014-05-27T11:30:03Z2014-05-27T11:30:03Z2013-07-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1186/scrt236Stem Cell Research and Therapy, v. 4, n. 4, 2013.1757-6512http://hdl.handle.net/11449/7605110.1186/scrt236WOS:0003231744000012-s2.0-848803353472-s2.0-84880335347.pdf964343370616394660209849378498017773733250141398Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengStem Cell Research and Therapy4.9631,685info:eu-repo/semantics/openAccess2024-09-09T14:01:09Zoai:repositorio.unesp.br:11449/76051Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-09T14:01:09Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial |
title |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial |
spellingShingle |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial Carvalho, Armando de Mattos [UNESP] Horse Stem cell Tendon lesion Treatment collagen fiber collagen type 1 membrane protein phosphate buffered saline scleraxis tenascin tenomodulin unclassified drug adipose tissue animal cell animal experiment animal tissue autologous stem cell transplantation blood flow cell isolation clinical evaluation COL1A1 gene COL3A1 gene controlled study digital flxeor tendon therapy Doppler flowmeter equine tendonitis female gene gene expression histopathology horse disease image analysis immunohistochemistry inflammatory infiltrate male mesenchymal stem cell transplantation nonhuman physical activity priority journal prophylaxis randomized controlled trial SCX gene tendinitis tendon thrombocyte transfusion tnc gene TNMD gene treatment outcome treatment response ultrasound Animalia Equidae |
title_short |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial |
title_full |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial |
title_fullStr |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial |
title_full_unstemmed |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial |
title_sort |
Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial |
author |
Carvalho, Armando de Mattos [UNESP] |
author_facet |
Carvalho, Armando de Mattos [UNESP] Badial, Peres Ramos [UNESP] Álvarez, Luis Emiliano Cisneros [UNESP] Yamada, Ana Lucia Miluzzi [UNESP] Borges, Alexandre Secorun [UNESP] Deffune, Elenice [UNESP] Hussni, Carlos Alberto [UNESP] Alves, Ana Liz Garcia [UNESP] |
author_role |
author |
author2 |
Badial, Peres Ramos [UNESP] Álvarez, Luis Emiliano Cisneros [UNESP] Yamada, Ana Lucia Miluzzi [UNESP] Borges, Alexandre Secorun [UNESP] Deffune, Elenice [UNESP] Hussni, Carlos Alberto [UNESP] Alves, Ana Liz Garcia [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Carvalho, Armando de Mattos [UNESP] Badial, Peres Ramos [UNESP] Álvarez, Luis Emiliano Cisneros [UNESP] Yamada, Ana Lucia Miluzzi [UNESP] Borges, Alexandre Secorun [UNESP] Deffune, Elenice [UNESP] Hussni, Carlos Alberto [UNESP] Alves, Ana Liz Garcia [UNESP] |
dc.subject.por.fl_str_mv |
Horse Stem cell Tendon lesion Treatment collagen fiber collagen type 1 membrane protein phosphate buffered saline scleraxis tenascin tenomodulin unclassified drug adipose tissue animal cell animal experiment animal tissue autologous stem cell transplantation blood flow cell isolation clinical evaluation COL1A1 gene COL3A1 gene controlled study digital flxeor tendon therapy Doppler flowmeter equine tendonitis female gene gene expression histopathology horse disease image analysis immunohistochemistry inflammatory infiltrate male mesenchymal stem cell transplantation nonhuman physical activity priority journal prophylaxis randomized controlled trial SCX gene tendinitis tendon thrombocyte transfusion tnc gene TNMD gene treatment outcome treatment response ultrasound Animalia Equidae |
topic |
Horse Stem cell Tendon lesion Treatment collagen fiber collagen type 1 membrane protein phosphate buffered saline scleraxis tenascin tenomodulin unclassified drug adipose tissue animal cell animal experiment animal tissue autologous stem cell transplantation blood flow cell isolation clinical evaluation COL1A1 gene COL3A1 gene controlled study digital flxeor tendon therapy Doppler flowmeter equine tendonitis female gene gene expression histopathology horse disease image analysis immunohistochemistry inflammatory infiltrate male mesenchymal stem cell transplantation nonhuman physical activity priority journal prophylaxis randomized controlled trial SCX gene tendinitis tendon thrombocyte transfusion tnc gene TNMD gene treatment outcome treatment response ultrasound Animalia Equidae |
description |
Introduction. Tendon injury is a major cause of lameness and decreased performance in athletic equines. Various therapies for tendonitis have been described; however, none of these therapies results in complete tissue regeneration, and the injury recurrence rate is high even after long recovery periods involving rest and physiotherapy. Methods. A lesion was induced with collagenase gel in the superficial digital flexor tendon in the center portion of the metacarpal region of eight equines of mixed breed. After two weeks, the lesions of the animals in the treated and control groups were treated through the intralesional administration of mesenchymal stem cells derived from adipose tissue (adMSCs) suspended in platelet concentrate (PC) and with phosphate buffered saline (PBS), respectively. Serial ultrasound analyses were performed every two weeks. After 16 weeks of therapy, a biopsy was performed for histopathological, immunohistochemical and gene expression (type I collagen (COL1A1), type III collagen (COL3A1), tenascin-C (TNC), tenomodulin (TNMD), and scleraxis (SCX)) analyses. Results: Differences in the ultrasound and histopathological analyses were observed between the groups. Improved results were reported in the group treated with adMSCs suspended in PC. There was no difference in the gene expression levels observed after the different treatments. The main results observed from the histopathological evaluation of the treated group were as follows: a prevention of the progression of the lesion, a greater organization of collagen fibers, and a decreased inflammatory infiltrate. A lack of progression of the lesion area and its percentage was observed in the ultrasound image, and increased blood flow was measured by Power Doppler. Conclusions: The use of adMSCs combined with PC for the therapy of experimentally induced tendonitis prevented the progression of the tendon lesion, as observed in the ultrasound examination, and resulted in a greater organization and decreased inflammation, as observed in the histopathological evaluation. These data demonstrate the therapeutic potential of this therapy for the treatment of equine tendonitis. © 2013 Carvalho et al.; licensee BioMed Central Ltd. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-07-25 2014-05-27T11:30:03Z 2014-05-27T11:30:03Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1186/scrt236 Stem Cell Research and Therapy, v. 4, n. 4, 2013. 1757-6512 http://hdl.handle.net/11449/76051 10.1186/scrt236 WOS:000323174400001 2-s2.0-84880335347 2-s2.0-84880335347.pdf 9643433706163946 6020984937849801 7773733250141398 |
url |
http://dx.doi.org/10.1186/scrt236 http://hdl.handle.net/11449/76051 |
identifier_str_mv |
Stem Cell Research and Therapy, v. 4, n. 4, 2013. 1757-6512 10.1186/scrt236 WOS:000323174400001 2-s2.0-84880335347 2-s2.0-84880335347.pdf 9643433706163946 6020984937849801 7773733250141398 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Stem Cell Research and Therapy 4.963 1,685 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1813546572920651776 |