L-threonine supplementation during colitis onset delays disease recovery

Detalhes bibliográficos
Autor(a) principal: Gaifem, Joana
Data de Publicação: 2018
Outros Autores: Gonçalves, Luís G., Dinis-Oliveira, Ricardo J., Cunha, Cristina, Carvalho, Agostinho, Torrado, Egídio, Rodrigues, Fernando, Saraiva, Margarida, Castro, António G., Silvestre, Ricardo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.3389/fphys.2018.01247
Resumo: Dietary nutrients have emerged as potential therapeutic adjuncts for inflammatory bowel disease (IBD) given their impact on intestinal homeostasis through the modulation of immune response, gut microbiota composition and epithelial barrier stability. Several nutrients have already been associated with a protective phenotype. Yet, there is a lack of knowledge toward the most promising ones as well as the most adequate phase of action. To unveil the most prominent therapy candidates we characterized the colon metabolic profile during colitis development. We have observed a twofold decrease in threonine levels in mice subjected to DSS-induced colitis. We then assessed the effect of threonine supplementation in the beginning of the inflammatory process (DSS + Thr) or when inflammation is already established (DSS + Thr D8). Colitis progression was similar between the treated groups and control colitic mice, yet threonine had a surprisingly detrimental effect when administered in the beginning of the disease, with mice displaying a delayed recovery when compared to control mice and mice supplemented with threonine after day 8. Although no major changes were found in their metabolic profile, DSS + Thr mice displayed altered expression in mucin-encoding genes, as well as in goblet cell counts, unveiling an impaired ability to produce mucus. Moreover, IL-22 secretion was decreased in DSS + Thr mice when compared to DSS + Thr D8 mice. Overall, these results suggest that supplementation with threonine during colitis induction impact goblet cell number and delays the recovery period. This reinforces the importance of a deeper understanding regarding threonine supplementation in IBD.
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spelling L-threonine supplementation during colitis onset delays disease recoveryDSS-induced colitisGoblet cellsIBDIL-22MetabolomicsMucinThreoninePhysiologyPhysiology (medical)Dietary nutrients have emerged as potential therapeutic adjuncts for inflammatory bowel disease (IBD) given their impact on intestinal homeostasis through the modulation of immune response, gut microbiota composition and epithelial barrier stability. Several nutrients have already been associated with a protective phenotype. Yet, there is a lack of knowledge toward the most promising ones as well as the most adequate phase of action. To unveil the most prominent therapy candidates we characterized the colon metabolic profile during colitis development. We have observed a twofold decrease in threonine levels in mice subjected to DSS-induced colitis. We then assessed the effect of threonine supplementation in the beginning of the inflammatory process (DSS + Thr) or when inflammation is already established (DSS + Thr D8). Colitis progression was similar between the treated groups and control colitic mice, yet threonine had a surprisingly detrimental effect when administered in the beginning of the disease, with mice displaying a delayed recovery when compared to control mice and mice supplemented with threonine after day 8. Although no major changes were found in their metabolic profile, DSS + Thr mice displayed altered expression in mucin-encoding genes, as well as in goblet cell counts, unveiling an impaired ability to produce mucus. Moreover, IL-22 secretion was decreased in DSS + Thr mice when compared to DSS + Thr D8 mice. Overall, these results suggest that supplementation with threonine during colitis induction impact goblet cell number and delays the recovery period. This reinforces the importance of a deeper understanding regarding threonine supplementation in IBD.Molecular, Structural and Cellular Microbiology (MOSTMICRO)Instituto de Tecnologia Química e Biológica António Xavier (ITQB)RUNGaifem, JoanaGonçalves, Luís G.Dinis-Oliveira, Ricardo J.Cunha, CristinaCarvalho, AgostinhoTorrado, EgídioRodrigues, FernandoSaraiva, MargaridaCastro, António G.Silvestre, Ricardo2019-04-26T22:14:35Z2018-09-052018-09-05T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.3389/fphys.2018.01247eng1664-042XPURE: 12428541http://www.scopus.com/inward/record.url?scp=85053078274&partnerID=8YFLogxKhttps://doi.org/10.3389/fphys.2018.01247info: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:RCAAP2024-03-11T04:32:02Zoai:run.unl.pt:10362/67802Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:34:40.115618Repositório 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 L-threonine supplementation during colitis onset delays disease recovery
title L-threonine supplementation during colitis onset delays disease recovery
spellingShingle L-threonine supplementation during colitis onset delays disease recovery
Gaifem, Joana
DSS-induced colitis
Goblet cells
IBD
IL-22
Metabolomics
Mucin
Threonine
Physiology
Physiology (medical)
title_short L-threonine supplementation during colitis onset delays disease recovery
title_full L-threonine supplementation during colitis onset delays disease recovery
title_fullStr L-threonine supplementation during colitis onset delays disease recovery
title_full_unstemmed L-threonine supplementation during colitis onset delays disease recovery
title_sort L-threonine supplementation during colitis onset delays disease recovery
author Gaifem, Joana
author_facet Gaifem, Joana
Gonçalves, Luís G.
Dinis-Oliveira, Ricardo J.
Cunha, Cristina
Carvalho, Agostinho
Torrado, Egídio
Rodrigues, Fernando
Saraiva, Margarida
Castro, António G.
Silvestre, Ricardo
author_role author
author2 Gonçalves, Luís G.
Dinis-Oliveira, Ricardo J.
Cunha, Cristina
Carvalho, Agostinho
Torrado, Egídio
Rodrigues, Fernando
Saraiva, Margarida
Castro, António G.
Silvestre, Ricardo
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Molecular, Structural and Cellular Microbiology (MOSTMICRO)
Instituto de Tecnologia Química e Biológica António Xavier (ITQB)
RUN
dc.contributor.author.fl_str_mv Gaifem, Joana
Gonçalves, Luís G.
Dinis-Oliveira, Ricardo J.
Cunha, Cristina
Carvalho, Agostinho
Torrado, Egídio
Rodrigues, Fernando
Saraiva, Margarida
Castro, António G.
Silvestre, Ricardo
dc.subject.por.fl_str_mv DSS-induced colitis
Goblet cells
IBD
IL-22
Metabolomics
Mucin
Threonine
Physiology
Physiology (medical)
topic DSS-induced colitis
Goblet cells
IBD
IL-22
Metabolomics
Mucin
Threonine
Physiology
Physiology (medical)
description Dietary nutrients have emerged as potential therapeutic adjuncts for inflammatory bowel disease (IBD) given their impact on intestinal homeostasis through the modulation of immune response, gut microbiota composition and epithelial barrier stability. Several nutrients have already been associated with a protective phenotype. Yet, there is a lack of knowledge toward the most promising ones as well as the most adequate phase of action. To unveil the most prominent therapy candidates we characterized the colon metabolic profile during colitis development. We have observed a twofold decrease in threonine levels in mice subjected to DSS-induced colitis. We then assessed the effect of threonine supplementation in the beginning of the inflammatory process (DSS + Thr) or when inflammation is already established (DSS + Thr D8). Colitis progression was similar between the treated groups and control colitic mice, yet threonine had a surprisingly detrimental effect when administered in the beginning of the disease, with mice displaying a delayed recovery when compared to control mice and mice supplemented with threonine after day 8. Although no major changes were found in their metabolic profile, DSS + Thr mice displayed altered expression in mucin-encoding genes, as well as in goblet cell counts, unveiling an impaired ability to produce mucus. Moreover, IL-22 secretion was decreased in DSS + Thr mice when compared to DSS + Thr D8 mice. Overall, these results suggest that supplementation with threonine during colitis induction impact goblet cell number and delays the recovery period. This reinforces the importance of a deeper understanding regarding threonine supplementation in IBD.
publishDate 2018
dc.date.none.fl_str_mv 2018-09-05
2018-09-05T00:00:00Z
2019-04-26T22:14:35Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv https://doi.org/10.3389/fphys.2018.01247
url https://doi.org/10.3389/fphys.2018.01247
dc.language.iso.fl_str_mv eng
language eng
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PURE: 12428541
http://www.scopus.com/inward/record.url?scp=85053078274&partnerID=8YFLogxK
https://doi.org/10.3389/fphys.2018.01247
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 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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