Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial

Detalhes bibliográficos
Autor(a) principal: Carvalho, Armando de Mattos [UNESP]
Data de Publicação: 2013
Outros Autores: 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]
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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spelling 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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