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Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays
The objective of the study was the evaluation of the potential pleiotropic effect of a commercial casein hydrolysate (CH). After an analysis of the composition, the BIOPEP-UWM database suggested that these peptides contained numerous sequences with potential inhibitory activities on angiotensin conv...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240083/ https://www.ncbi.nlm.nih.gov/pubmed/37284652 http://dx.doi.org/10.3389/fnut.2023.1198258 |
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author | Li, Jianqiang Bollati, Carlotta Aiello, Gilda Bartolomei, Martina Rivardo, Fabrizio Boschin, Giovanna Arnoldi, Anna Lammi, Carmen |
author_facet | Li, Jianqiang Bollati, Carlotta Aiello, Gilda Bartolomei, Martina Rivardo, Fabrizio Boschin, Giovanna Arnoldi, Anna Lammi, Carmen |
author_sort | Li, Jianqiang |
collection | PubMed |
description | The objective of the study was the evaluation of the potential pleiotropic effect of a commercial casein hydrolysate (CH). After an analysis of the composition, the BIOPEP-UWM database suggested that these peptides contained numerous sequences with potential inhibitory activities on angiotensin converting enzyme (ACE) and dipeptidyl-peptidase IV (DPP-IV). The anti-diabetic and anti-hypertensive effects of these peptides were thus assessed using either cell-free or cell-based assays. In the cell-free system, CH displayed inhibitory properties against DPP-IV (IC(50) value equal to 0.38 ± 0.01 mg/mL) and ACE (IC(50) value equal to 0.39 ± 0.01 mg/mL). Further, CH reduced the DPP-IV and ACE activities expressed by human intestinal Caco-2 cells by 61.10 ± 1.70% and 76.90 ± 4.47%, respectively, versus untreated cells, after 6 h of treatment at the concentration of 5 mg/mL. This first demonstration of the multifunctional behavior of this material suggests that it may become an anti-diabetic and/or anti-hypertensive ingredient to be included in the formulation of different functional food or nutraceutics. |
format | Online Article Text |
id | pubmed-10240083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102400832023-06-06 Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays Li, Jianqiang Bollati, Carlotta Aiello, Gilda Bartolomei, Martina Rivardo, Fabrizio Boschin, Giovanna Arnoldi, Anna Lammi, Carmen Front Nutr Nutrition The objective of the study was the evaluation of the potential pleiotropic effect of a commercial casein hydrolysate (CH). After an analysis of the composition, the BIOPEP-UWM database suggested that these peptides contained numerous sequences with potential inhibitory activities on angiotensin converting enzyme (ACE) and dipeptidyl-peptidase IV (DPP-IV). The anti-diabetic and anti-hypertensive effects of these peptides were thus assessed using either cell-free or cell-based assays. In the cell-free system, CH displayed inhibitory properties against DPP-IV (IC(50) value equal to 0.38 ± 0.01 mg/mL) and ACE (IC(50) value equal to 0.39 ± 0.01 mg/mL). Further, CH reduced the DPP-IV and ACE activities expressed by human intestinal Caco-2 cells by 61.10 ± 1.70% and 76.90 ± 4.47%, respectively, versus untreated cells, after 6 h of treatment at the concentration of 5 mg/mL. This first demonstration of the multifunctional behavior of this material suggests that it may become an anti-diabetic and/or anti-hypertensive ingredient to be included in the formulation of different functional food or nutraceutics. Frontiers Media S.A. 2023-05-22 /pmc/articles/PMC10240083/ /pubmed/37284652 http://dx.doi.org/10.3389/fnut.2023.1198258 Text en Copyright © 2023 Li, Bollati, Aiello, Bartolomei, Rivardo, Boschin, Arnoldi and Lammi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Nutrition Li, Jianqiang Bollati, Carlotta Aiello, Gilda Bartolomei, Martina Rivardo, Fabrizio Boschin, Giovanna Arnoldi, Anna Lammi, Carmen Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays |
title | Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays |
title_full | Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays |
title_fullStr | Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays |
title_full_unstemmed | Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays |
title_short | Evaluation of the multifunctional dipeptidyl-peptidase IV and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays |
title_sort | evaluation of the multifunctional dipeptidyl-peptidase iv and angiotensin converting enzyme inhibitory properties of a casein hydrolysate using cell-free and cell-based assays |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240083/ https://www.ncbi.nlm.nih.gov/pubmed/37284652 http://dx.doi.org/10.3389/fnut.2023.1198258 |
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