Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice

Detalhes bibliográficos
Autor(a) principal: Tran, Dung Huu
Data de Publicação: 2023
Outros Autores: Thuy, Phan Kim, Hien, Chu Thi Thu, Chau, Thai Khoa Bao, Tien, Nguyen Huu, Toan, Nguyen Van Thanh
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/208743
Resumo: Recently, the acetate wheat starch (AWS) has been prepared by acetylation with an acetyl content of 2.42%, containing of rapidly digestible starch (RDS), slowly digestible starch (SDS) and resistant starch (RS) with 25.0%; 22.9% and 34.5%, respectively. In this study, this kind of starch was continuously evaluated with the postprandial blood glucose response and determined short-chain fatty acids (SCFAs) metabolized from AWS in the gastrointestinal tract of healthy mice by HPLC. The result showed that the mice fed with AWS exhibited a very limited increase in blood glucose level and remained stable for 2 hours after meals efficiently comparing with the control group fed with natural wheat starch (NWS). Simultaneously, the content of SCFAs produced in the caecum of the mice fed with AWS was significantly higher than mice fed with NWS, especially with acetic and propionic acids by 28% and 26%, respectively. Thus, AWS has shown to limit the postprandial hyperglycemia in mice effectively through the resistance to amylase hydrolysis in the small intestine. When going into the caecum, it is fermented to form SCFAs providing a part of energy for the body’s activities, avoiding rotten fermentation causing digestive disorders which are inherent restrictions of normal high cellulose and fiber food.
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spelling Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy miceAcetate wheat starchGlucoseSCFACaecumRecently, the acetate wheat starch (AWS) has been prepared by acetylation with an acetyl content of 2.42%, containing of rapidly digestible starch (RDS), slowly digestible starch (SDS) and resistant starch (RS) with 25.0%; 22.9% and 34.5%, respectively. In this study, this kind of starch was continuously evaluated with the postprandial blood glucose response and determined short-chain fatty acids (SCFAs) metabolized from AWS in the gastrointestinal tract of healthy mice by HPLC. The result showed that the mice fed with AWS exhibited a very limited increase in blood glucose level and remained stable for 2 hours after meals efficiently comparing with the control group fed with natural wheat starch (NWS). Simultaneously, the content of SCFAs produced in the caecum of the mice fed with AWS was significantly higher than mice fed with NWS, especially with acetic and propionic acids by 28% and 26%, respectively. Thus, AWS has shown to limit the postprandial hyperglycemia in mice effectively through the resistance to amylase hydrolysis in the small intestine. When going into the caecum, it is fermented to form SCFAs providing a part of energy for the body’s activities, avoiding rotten fermentation causing digestive disorders which are inherent restrictions of normal high cellulose and fiber food.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2023-02-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/20874310.1590/s2175-97902020000118837Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/208743/194965Copyright (c) 2022 Brazilian Journal of Pharmaceutical Scienceshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessTran, Dung HuuThuy, Phan Kim Hien, Chu Thi Thu Chau, Thai Khoa Bao Tien, Nguyen Huu Toan, Nguyen Van Thanh 2023-08-18T21:00:06Zoai:revistas.usp.br:article/208743Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-08-18T21:00:06Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
title Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
spellingShingle Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
Tran, Dung Huu
Acetate wheat starch
Glucose
SCFA
Caecum
title_short Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
title_full Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
title_fullStr Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
title_full_unstemmed Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
title_sort Effects of reducing postprandial hyperglycemia and metabolism of acetate wheat starch on healthy mice
author Tran, Dung Huu
author_facet Tran, Dung Huu
Thuy, Phan Kim
Hien, Chu Thi Thu
Chau, Thai Khoa Bao
Tien, Nguyen Huu
Toan, Nguyen Van Thanh
author_role author
author2 Thuy, Phan Kim
Hien, Chu Thi Thu
Chau, Thai Khoa Bao
Tien, Nguyen Huu
Toan, Nguyen Van Thanh
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Tran, Dung Huu
Thuy, Phan Kim
Hien, Chu Thi Thu
Chau, Thai Khoa Bao
Tien, Nguyen Huu
Toan, Nguyen Van Thanh
dc.subject.por.fl_str_mv Acetate wheat starch
Glucose
SCFA
Caecum
topic Acetate wheat starch
Glucose
SCFA
Caecum
description Recently, the acetate wheat starch (AWS) has been prepared by acetylation with an acetyl content of 2.42%, containing of rapidly digestible starch (RDS), slowly digestible starch (SDS) and resistant starch (RS) with 25.0%; 22.9% and 34.5%, respectively. In this study, this kind of starch was continuously evaluated with the postprandial blood glucose response and determined short-chain fatty acids (SCFAs) metabolized from AWS in the gastrointestinal tract of healthy mice by HPLC. The result showed that the mice fed with AWS exhibited a very limited increase in blood glucose level and remained stable for 2 hours after meals efficiently comparing with the control group fed with natural wheat starch (NWS). Simultaneously, the content of SCFAs produced in the caecum of the mice fed with AWS was significantly higher than mice fed with NWS, especially with acetic and propionic acids by 28% and 26%, respectively. Thus, AWS has shown to limit the postprandial hyperglycemia in mice effectively through the resistance to amylase hydrolysis in the small intestine. When going into the caecum, it is fermented to form SCFAs providing a part of energy for the body’s activities, avoiding rotten fermentation causing digestive disorders which are inherent restrictions of normal high cellulose and fiber food.
publishDate 2023
dc.date.none.fl_str_mv 2023-02-28
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjps/article/view/208743
10.1590/s2175-97902020000118837
url https://www.revistas.usp.br/bjps/article/view/208743
identifier_str_mv 10.1590/s2175-97902020000118837
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/208743/194965
dc.rights.driver.fl_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)
Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022)
Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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