Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/108205 https://doi.org/10.20960/nh.1326 |
Resumo: | Background: Teduglutide is an enterotrophic analogue of glucagon-like peptide-2, with an indirect and poorly understood mechanism of action, approved for the rehabilitation of short-bowel syndrome. This study aims to analyze the response of tissue growth factors to surgical injury and teduglutide administration on an animal model of intestinal anastomosis. Methods: Wistar rats (n = 59) were distributed into four groups: “ileal resection” or “laparotomy”, each one subdivided into “postoperative teduglutide administration” or “no treatment”; and sacrificed at the third or the seventh day, with ileal sample harvesting. Gene expression of insulin-like growth factor 1 (Igf1), vascular endothelial growth factor a (Vegfa), transforming growth factor β1 (Tgfβ1), connective tissue growth factor (Ctgf), fibroblast growth factor 2 (Fgf2), fibroblast growth factor 7 (Fgf7), epidermal growth factor (Egf), heparin-binding epidermal-like growth factor (Hbegf), platelet-derived growth factor b (Pdgfb) and glucagon-like peptide 2 receptor (Glp2r) was studied by real-time polymerase chain reaction. Results: Upregulation of Fgf7, Fgf2, Egf, Vegfa and Glp2r at the third day and of Pdgf at the seventh day was verified in the perianastomotic segment. Teduglutide administration was associated with higher fold-change of relative gene expression of Vegfa (3.6 ± 1.3 vs. 1.9 ± 2.0, p = 0.0001), Hbegf (2.2 ± 2.3 vs. 1.1 ± 0.9, p = 0.001), Igf1 (1.6 ± 7.6 vs. 0.9 ± 0.7, p = 0.002) and Ctgf (1.1 ± 2.1 vs. 0.6 ± 2.0, p = 0.013); and lower fold-change of Tgfβ1, Fgf7 and Glp2r. Conclusions: Those results underscore the recognized role of Igf1 and Hbegf as molecular mediators of the effects of teduglutide and suggest that other humoral factors, like Vegf and Ctgf, may also be relevant in the perioperative context. Induction of Vegfa, Igf1 and Ctgf gene expressions might indicate a favorable influence of teduglutide on the intestinal anastomotic healing. |
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Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosisPerfil tisular de factores de crecimiento postadministración de teduglutida en un modelo animal de anastomosis intestinalTeduglutideGrowth factorsIntestinal anastomosisVascular endothelial growth factorConnective tissue growth factorTeduglutidaFactores de crecimientoAnastomosis intestinalFactor de crecimiento vascular endotelialFactor de crecimiento del tejido conectivoAnimalsGastrointestinal AgentsGene Expression RegulationIleumIntercellular Signaling Peptides and ProteinsIntestinesMalePeptidesRatsRats, WistarShort Bowel SyndromeAnastomosis, SurgicalBackground: Teduglutide is an enterotrophic analogue of glucagon-like peptide-2, with an indirect and poorly understood mechanism of action, approved for the rehabilitation of short-bowel syndrome. This study aims to analyze the response of tissue growth factors to surgical injury and teduglutide administration on an animal model of intestinal anastomosis. Methods: Wistar rats (n = 59) were distributed into four groups: “ileal resection” or “laparotomy”, each one subdivided into “postoperative teduglutide administration” or “no treatment”; and sacrificed at the third or the seventh day, with ileal sample harvesting. Gene expression of insulin-like growth factor 1 (Igf1), vascular endothelial growth factor a (Vegfa), transforming growth factor β1 (Tgfβ1), connective tissue growth factor (Ctgf), fibroblast growth factor 2 (Fgf2), fibroblast growth factor 7 (Fgf7), epidermal growth factor (Egf), heparin-binding epidermal-like growth factor (Hbegf), platelet-derived growth factor b (Pdgfb) and glucagon-like peptide 2 receptor (Glp2r) was studied by real-time polymerase chain reaction. Results: Upregulation of Fgf7, Fgf2, Egf, Vegfa and Glp2r at the third day and of Pdgf at the seventh day was verified in the perianastomotic segment. Teduglutide administration was associated with higher fold-change of relative gene expression of Vegfa (3.6 ± 1.3 vs. 1.9 ± 2.0, p = 0.0001), Hbegf (2.2 ± 2.3 vs. 1.1 ± 0.9, p = 0.001), Igf1 (1.6 ± 7.6 vs. 0.9 ± 0.7, p = 0.002) and Ctgf (1.1 ± 2.1 vs. 0.6 ± 2.0, p = 0.013); and lower fold-change of Tgfβ1, Fgf7 and Glp2r. Conclusions: Those results underscore the recognized role of Igf1 and Hbegf as molecular mediators of the effects of teduglutide and suggest that other humoral factors, like Vegf and Ctgf, may also be relevant in the perioperative context. Induction of Vegfa, Igf1 and Ctgf gene expressions might indicate a favorable influence of teduglutide on the intestinal anastomotic healing.Introducción: teduglutida es un análogo intestinotrófico do péptido-2 similar al glucagón, con un mecanismo de acción indirecto y poco conocido, aprobado para la rehabilitación del síndrome de intestino corto. Este estudio propone analizar la respuesta de los factores de crecimiento tisulares a la agresión quirúrgica y a la administración de teduglutida en un modelo animal de anastomosis intestinal. Métodos: ratones Wistar (n = 59) fueron distribuidos en cuatro grupos: "resección ileal" o "laparotomía", cada uno subdividido en "administración post-operatoria de teduglutida" o "sin tratamiento"; y sacrificados en el tercero o el séptimo día, con recogida de muestras ileales. La expresión génica de Igf1, Vegfa, Tgfβ1, Ctgf, Fgf2, Fgf7, Egf, Hbegf, Pdgfb y Glp2r fue analizada por qRT-PCR. Resultados: en el segmento perianastomótico se verificó una sobrerregulación de Fgf7, Fgf2, Egf, Vegfa y Glp2r al tercer día y de Pdg al séptimo día. La administración de teduglutida se asoció con mayor cambio de la expresión génica relativa de Vegfa (3.6 ± 1.3 vs. 1.9 ± 2.0, p = 0.0001), Hbegf (2.2 ± 2.3 vs. 1.1 ± 0.9, p = 0.001), Igf1 (1.6 ± 7.6 vs. 0.9 ± 0.7, p = 0.002) y Ctgf (1.1 ± 2.1 vs. 0.6 ± 2.0, p = 0.013); y menor cambio de Tgfβ1, Fgf7 y Glp2r. Conclusiones: estos resultados refuerzan el reconocido papel de Igf1 y Hbegf como mediadores moleculares de los efectos de la teduglutida y sugieren que otros factores humorales, como Vegf y Ctgf, también pueden ser relevantes en el contexto perioperatorio. La inducción de las expresiones de los genes Vegfa, Igf1 y Ctgf podría indicar una influencia favorable de teduglutida en la cicatrización anastomótica intestinal.Grupo Aula Medica S.A.2018-01-16info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/108205http://hdl.handle.net/10316/108205https://doi.org/10.20960/nh.1326eng1699-51980212-1611Costa, Beatriz P.Gonçalves, Ana C.Abrantes, Ana M.Alves, RaquelMatafome, Paulo N.Seiça, RaquelRibeiro, Ana B. SarmentoBotelho, M. FilomenaCastro-Sousa, Franciscoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-08-17T08:19:04Zoai:estudogeral.uc.pt:10316/108205Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:24:06.157387Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis Perfil tisular de factores de crecimiento postadministración de teduglutida en un modelo animal de anastomosis intestinal |
title |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis |
spellingShingle |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis Costa, Beatriz P. Teduglutide Growth factors Intestinal anastomosis Vascular endothelial growth factor Connective tissue growth factor Teduglutida Factores de crecimiento Anastomosis intestinal Factor de crecimiento vascular endotelial Factor de crecimiento del tejido conectivo Animals Gastrointestinal Agents Gene Expression Regulation Ileum Intercellular Signaling Peptides and Proteins Intestines Male Peptides Rats Rats, Wistar Short Bowel Syndrome Anastomosis, Surgical |
title_short |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis |
title_full |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis |
title_fullStr |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis |
title_full_unstemmed |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis |
title_sort |
Tissular growth factors profile after teduglutide administration on an animal model of intestinal anastomosis |
author |
Costa, Beatriz P. |
author_facet |
Costa, Beatriz P. Gonçalves, Ana C. Abrantes, Ana M. Alves, Raquel Matafome, Paulo N. Seiça, Raquel Ribeiro, Ana B. Sarmento Botelho, M. Filomena Castro-Sousa, Francisco |
author_role |
author |
author2 |
Gonçalves, Ana C. Abrantes, Ana M. Alves, Raquel Matafome, Paulo N. Seiça, Raquel Ribeiro, Ana B. Sarmento Botelho, M. Filomena Castro-Sousa, Francisco |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Costa, Beatriz P. Gonçalves, Ana C. Abrantes, Ana M. Alves, Raquel Matafome, Paulo N. Seiça, Raquel Ribeiro, Ana B. Sarmento Botelho, M. Filomena Castro-Sousa, Francisco |
dc.subject.por.fl_str_mv |
Teduglutide Growth factors Intestinal anastomosis Vascular endothelial growth factor Connective tissue growth factor Teduglutida Factores de crecimiento Anastomosis intestinal Factor de crecimiento vascular endotelial Factor de crecimiento del tejido conectivo Animals Gastrointestinal Agents Gene Expression Regulation Ileum Intercellular Signaling Peptides and Proteins Intestines Male Peptides Rats Rats, Wistar Short Bowel Syndrome Anastomosis, Surgical |
topic |
Teduglutide Growth factors Intestinal anastomosis Vascular endothelial growth factor Connective tissue growth factor Teduglutida Factores de crecimiento Anastomosis intestinal Factor de crecimiento vascular endotelial Factor de crecimiento del tejido conectivo Animals Gastrointestinal Agents Gene Expression Regulation Ileum Intercellular Signaling Peptides and Proteins Intestines Male Peptides Rats Rats, Wistar Short Bowel Syndrome Anastomosis, Surgical |
description |
Background: Teduglutide is an enterotrophic analogue of glucagon-like peptide-2, with an indirect and poorly understood mechanism of action, approved for the rehabilitation of short-bowel syndrome. This study aims to analyze the response of tissue growth factors to surgical injury and teduglutide administration on an animal model of intestinal anastomosis. Methods: Wistar rats (n = 59) were distributed into four groups: “ileal resection” or “laparotomy”, each one subdivided into “postoperative teduglutide administration” or “no treatment”; and sacrificed at the third or the seventh day, with ileal sample harvesting. Gene expression of insulin-like growth factor 1 (Igf1), vascular endothelial growth factor a (Vegfa), transforming growth factor β1 (Tgfβ1), connective tissue growth factor (Ctgf), fibroblast growth factor 2 (Fgf2), fibroblast growth factor 7 (Fgf7), epidermal growth factor (Egf), heparin-binding epidermal-like growth factor (Hbegf), platelet-derived growth factor b (Pdgfb) and glucagon-like peptide 2 receptor (Glp2r) was studied by real-time polymerase chain reaction. Results: Upregulation of Fgf7, Fgf2, Egf, Vegfa and Glp2r at the third day and of Pdgf at the seventh day was verified in the perianastomotic segment. Teduglutide administration was associated with higher fold-change of relative gene expression of Vegfa (3.6 ± 1.3 vs. 1.9 ± 2.0, p = 0.0001), Hbegf (2.2 ± 2.3 vs. 1.1 ± 0.9, p = 0.001), Igf1 (1.6 ± 7.6 vs. 0.9 ± 0.7, p = 0.002) and Ctgf (1.1 ± 2.1 vs. 0.6 ± 2.0, p = 0.013); and lower fold-change of Tgfβ1, Fgf7 and Glp2r. Conclusions: Those results underscore the recognized role of Igf1 and Hbegf as molecular mediators of the effects of teduglutide and suggest that other humoral factors, like Vegf and Ctgf, may also be relevant in the perioperative context. Induction of Vegfa, Igf1 and Ctgf gene expressions might indicate a favorable influence of teduglutide on the intestinal anastomotic healing. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-01-16 |
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://hdl.handle.net/10316/108205 http://hdl.handle.net/10316/108205 https://doi.org/10.20960/nh.1326 |
url |
http://hdl.handle.net/10316/108205 https://doi.org/10.20960/nh.1326 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1699-5198 0212-1611 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Grupo Aula Medica S.A. |
publisher.none.fl_str_mv |
Grupo Aula Medica S.A. |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
|
_version_ |
1799134126509391872 |