Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides

Detalhes bibliográficos
Autor(a) principal: Henaux, Loïc
Data de Publicação: 2021
Outros Autores: Pereira, Karina Danielle [UNESP], Thibodeau, Jacinthe, Pilon, Geneviève, Gill, Tom, Marette, André, Bazinet, Laurent
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/membranes11070528
http://hdl.handle.net/11449/222057
Resumo: Natural bioactive peptides are suitable candidates for preventing the development of Type 2 diabetes (T2D), by reducing the various risk factors. The aim of this study was to concentrate glucoregulatory and anti-inflammatory peptides, from salmon by-products, by electrodialysis with ultrafiltration membrane (EDUF), and to identify peptides responsible for these bioactivities. Two EDUF configurations (1 and 2) were used to concentrate anionic and cationic peptides, respectively. After EDUF separation, two fractions demonstrated interesting properties: the initial fraction of the EDUF configuration 1 and the final fraction of the EDUF configuration 2 both showed biological activities to (1) increase glucose uptake in L6 muscle cells in insulin condition at 1 ng/mL (by 12% and 21%, respectively), (2) decrease hepatic glucose production in hepatic cells at 1 ng/mL in basal (17% and 16%, respectively), and insulin (25% and 34%, respectively) conditions, and (3) decrease LPS-induced inflammation in macrophages at 1 g/mL (45% and 30%, respectively). More impressive, the initial fraction of the EDUF configuration 1 (45% reduction) showed the same effect as the phenformin at 10 µM (40%), a drug used to treat T2D. Thirteen peptides were identified, chemically synthesized, and tested in-vitro for these three bioactivities. Thus, four new bioactive peptides were identified: IPVE increased glucose uptake by muscle cells, IVDI and IEGTL decreased hepatic glucose production (HGP) of insulin, whereas VAPEEHPTL decreased HGP under both basal condition and in the presence of insulin. To the best of our knowledge, this is the first time that (1) bioactive peptide fractions generated after separation by EDUF were demonstrated to be bioactive on three different criteria; all involved in the T2D, and (2) potential sequences involved in the improvement of glucose uptake and/or in the regulation of HGP were identified from a salmon protein hydrolysate.
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spelling Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptidesAnti-inflammatory activityBioactive peptidesElectrodialysis with filtration membraneGlucose uptakeHepatic glucose productionSalmon protein hydrolysateNatural bioactive peptides are suitable candidates for preventing the development of Type 2 diabetes (T2D), by reducing the various risk factors. The aim of this study was to concentrate glucoregulatory and anti-inflammatory peptides, from salmon by-products, by electrodialysis with ultrafiltration membrane (EDUF), and to identify peptides responsible for these bioactivities. Two EDUF configurations (1 and 2) were used to concentrate anionic and cationic peptides, respectively. After EDUF separation, two fractions demonstrated interesting properties: the initial fraction of the EDUF configuration 1 and the final fraction of the EDUF configuration 2 both showed biological activities to (1) increase glucose uptake in L6 muscle cells in insulin condition at 1 ng/mL (by 12% and 21%, respectively), (2) decrease hepatic glucose production in hepatic cells at 1 ng/mL in basal (17% and 16%, respectively), and insulin (25% and 34%, respectively) conditions, and (3) decrease LPS-induced inflammation in macrophages at 1 g/mL (45% and 30%, respectively). More impressive, the initial fraction of the EDUF configuration 1 (45% reduction) showed the same effect as the phenformin at 10 µM (40%), a drug used to treat T2D. Thirteen peptides were identified, chemically synthesized, and tested in-vitro for these three bioactivities. Thus, four new bioactive peptides were identified: IPVE increased glucose uptake by muscle cells, IVDI and IEGTL decreased hepatic glucose production (HGP) of insulin, whereas VAPEEHPTL decreased HGP under both basal condition and in the presence of insulin. To the best of our knowledge, this is the first time that (1) bioactive peptide fractions generated after separation by EDUF were demonstrated to be bioactive on three different criteria; all involved in the T2D, and (2) potential sequences involved in the improvement of glucose uptake and/or in the regulation of HGP were identified from a salmon protein hydrolysate.Canadian Institutes of Health ResearchDepartment of Food Sciences and Laboratory of Food Processing and Electromembrane Processes (LTAPEM) Université LavalInstitute of Nutrition and Functional Foods (INAF) University LavalLaboratory of Biotechnology School of Applied Sciences University of Campinas (UNICAMP)Institute of Biosciences State University (UNESP)Department of Medicine Faculty of Medicine Quebec Heart and Lung Institute Cardiology Group Université Laval, 2725 Chemin Ste-FoyDepartment of Process Engineering and Applied Science Dalhousie University, P.O. Box 15000Institute of Biosciences State University (UNESP)Canadian Institutes of Health Research: FH4-129922Université LavalUniversity LavalUniversidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (UNESP)Dalhousie UniversityHenaux, LoïcPereira, Karina Danielle [UNESP]Thibodeau, JacinthePilon, GenevièveGill, TomMarette, AndréBazinet, Laurent2022-04-28T19:42:08Z2022-04-28T19:42:08Z2021-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/membranes11070528Membranes, v. 11, n. 7, 2021.2077-0375http://hdl.handle.net/11449/22205710.3390/membranes110705282-s2.0-85111273791Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMembranesinfo:eu-repo/semantics/openAccess2022-04-28T19:42:08Zoai:repositorio.unesp.br:11449/222057Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:32:34.720118Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
title Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
spellingShingle Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
Henaux, Loïc
Anti-inflammatory activity
Bioactive peptides
Electrodialysis with filtration membrane
Glucose uptake
Hepatic glucose production
Salmon protein hydrolysate
title_short Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
title_full Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
title_fullStr Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
title_full_unstemmed Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
title_sort Glucoregulatory and anti-inflammatory activities of peptide fractions separated by electrodialysis with ultrafiltration membranes from salmon protein hydrolysate and identification of four novel glucoregulatory peptides
author Henaux, Loïc
author_facet Henaux, Loïc
Pereira, Karina Danielle [UNESP]
Thibodeau, Jacinthe
Pilon, Geneviève
Gill, Tom
Marette, André
Bazinet, Laurent
author_role author
author2 Pereira, Karina Danielle [UNESP]
Thibodeau, Jacinthe
Pilon, Geneviève
Gill, Tom
Marette, André
Bazinet, Laurent
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Université Laval
University Laval
Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (UNESP)
Dalhousie University
dc.contributor.author.fl_str_mv Henaux, Loïc
Pereira, Karina Danielle [UNESP]
Thibodeau, Jacinthe
Pilon, Geneviève
Gill, Tom
Marette, André
Bazinet, Laurent
dc.subject.por.fl_str_mv Anti-inflammatory activity
Bioactive peptides
Electrodialysis with filtration membrane
Glucose uptake
Hepatic glucose production
Salmon protein hydrolysate
topic Anti-inflammatory activity
Bioactive peptides
Electrodialysis with filtration membrane
Glucose uptake
Hepatic glucose production
Salmon protein hydrolysate
description Natural bioactive peptides are suitable candidates for preventing the development of Type 2 diabetes (T2D), by reducing the various risk factors. The aim of this study was to concentrate glucoregulatory and anti-inflammatory peptides, from salmon by-products, by electrodialysis with ultrafiltration membrane (EDUF), and to identify peptides responsible for these bioactivities. Two EDUF configurations (1 and 2) were used to concentrate anionic and cationic peptides, respectively. After EDUF separation, two fractions demonstrated interesting properties: the initial fraction of the EDUF configuration 1 and the final fraction of the EDUF configuration 2 both showed biological activities to (1) increase glucose uptake in L6 muscle cells in insulin condition at 1 ng/mL (by 12% and 21%, respectively), (2) decrease hepatic glucose production in hepatic cells at 1 ng/mL in basal (17% and 16%, respectively), and insulin (25% and 34%, respectively) conditions, and (3) decrease LPS-induced inflammation in macrophages at 1 g/mL (45% and 30%, respectively). More impressive, the initial fraction of the EDUF configuration 1 (45% reduction) showed the same effect as the phenformin at 10 µM (40%), a drug used to treat T2D. Thirteen peptides were identified, chemically synthesized, and tested in-vitro for these three bioactivities. Thus, four new bioactive peptides were identified: IPVE increased glucose uptake by muscle cells, IVDI and IEGTL decreased hepatic glucose production (HGP) of insulin, whereas VAPEEHPTL decreased HGP under both basal condition and in the presence of insulin. To the best of our knowledge, this is the first time that (1) bioactive peptide fractions generated after separation by EDUF were demonstrated to be bioactive on three different criteria; all involved in the T2D, and (2) potential sequences involved in the improvement of glucose uptake and/or in the regulation of HGP were identified from a salmon protein hydrolysate.
publishDate 2021
dc.date.none.fl_str_mv 2021-07-01
2022-04-28T19:42:08Z
2022-04-28T19:42:08Z
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/10.3390/membranes11070528
Membranes, v. 11, n. 7, 2021.
2077-0375
http://hdl.handle.net/11449/222057
10.3390/membranes11070528
2-s2.0-85111273791
url http://dx.doi.org/10.3390/membranes11070528
http://hdl.handle.net/11449/222057
identifier_str_mv Membranes, v. 11, n. 7, 2021.
2077-0375
10.3390/membranes11070528
2-s2.0-85111273791
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Membranes
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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
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