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Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects
In vitro and in vivo studies have reported the potential cardioprotective effects of fermented milks (FM). The aim of the present study was to evaluate the inhibitory activities of angiotensin converting enzyme (ACE), thrombin enzyme (TI) and micellar solubility of cholesterol of FM after 24 and 48 ...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122198/ https://www.ncbi.nlm.nih.gov/pubmed/37179799 http://dx.doi.org/10.1007/s13197-023-05715-1 |
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author | Zambrano-Cervantes, Miriam González-Córdova, Aarón F. Hernández-Mendoza, Adrián Beltrán-Barrientos, Lilia M. Rendón-Rosales, Miguel Á. Manzanarez-Quin, Carmen G. Torres-Llanez, María J. Vallejo-Cordoba, Belinda |
author_facet | Zambrano-Cervantes, Miriam González-Córdova, Aarón F. Hernández-Mendoza, Adrián Beltrán-Barrientos, Lilia M. Rendón-Rosales, Miguel Á. Manzanarez-Quin, Carmen G. Torres-Llanez, María J. Vallejo-Cordoba, Belinda |
author_sort | Zambrano-Cervantes, Miriam |
collection | PubMed |
description | In vitro and in vivo studies have reported the potential cardioprotective effects of fermented milks (FM). The aim of the present study was to evaluate the inhibitory activities of angiotensin converting enzyme (ACE), thrombin enzyme (TI) and micellar solubility of cholesterol of FM after 24 and 48 h of fermentation with Limosilactobacillus fermentum (J20, J23, J28 and J38), Lactiplantibacillus plantarum (J25) or Lactiplantibacillus pentosus (J34 and J37) exposed to simulated gastrointestinal digestion. Results showed that FM with J20 and J23 at 48 h of fermentation presented significantly (p < 0.05) higher degree of hydrolysis than other FM, and were not significantly different (p > 0.05) between them. Conversely, peptide relative abundance was significantly (p < 0.05) higher in FM with J20 than FM with J23. Moreover, IC(50) (protein concentration necessary to inhibit enzyme activity by 50%) for ACE inhibition were 0.33 and 0.5 mg/mL for FM with J20 and J23, respectively. For TI inhibition, the IC(50) were 0.3 and 0.24 mg/mL for FM with J20 and J23, respectively. Results exhibited 51 and 74% inhibition of micellar solubility cholesterol for FM with J20 and J23, respectively. Therefore, these results showed that not only peptide abundance, but also specific peptides might be responsible for these potential cardioprotective effects. |
format | Online Article Text |
id | pubmed-10122198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-101221982023-04-24 Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects Zambrano-Cervantes, Miriam González-Córdova, Aarón F. Hernández-Mendoza, Adrián Beltrán-Barrientos, Lilia M. Rendón-Rosales, Miguel Á. Manzanarez-Quin, Carmen G. Torres-Llanez, María J. Vallejo-Cordoba, Belinda J Food Sci Technol Original Article In vitro and in vivo studies have reported the potential cardioprotective effects of fermented milks (FM). The aim of the present study was to evaluate the inhibitory activities of angiotensin converting enzyme (ACE), thrombin enzyme (TI) and micellar solubility of cholesterol of FM after 24 and 48 h of fermentation with Limosilactobacillus fermentum (J20, J23, J28 and J38), Lactiplantibacillus plantarum (J25) or Lactiplantibacillus pentosus (J34 and J37) exposed to simulated gastrointestinal digestion. Results showed that FM with J20 and J23 at 48 h of fermentation presented significantly (p < 0.05) higher degree of hydrolysis than other FM, and were not significantly different (p > 0.05) between them. Conversely, peptide relative abundance was significantly (p < 0.05) higher in FM with J20 than FM with J23. Moreover, IC(50) (protein concentration necessary to inhibit enzyme activity by 50%) for ACE inhibition were 0.33 and 0.5 mg/mL for FM with J20 and J23, respectively. For TI inhibition, the IC(50) were 0.3 and 0.24 mg/mL for FM with J20 and J23, respectively. Results exhibited 51 and 74% inhibition of micellar solubility cholesterol for FM with J20 and J23, respectively. Therefore, these results showed that not only peptide abundance, but also specific peptides might be responsible for these potential cardioprotective effects. Springer India 2023-04-22 2023-06 /pmc/articles/PMC10122198/ /pubmed/37179799 http://dx.doi.org/10.1007/s13197-023-05715-1 Text en © Association of Food Scientists & Technologists (India) 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
spellingShingle | Original Article Zambrano-Cervantes, Miriam González-Córdova, Aarón F. Hernández-Mendoza, Adrián Beltrán-Barrientos, Lilia M. Rendón-Rosales, Miguel Á. Manzanarez-Quin, Carmen G. Torres-Llanez, María J. Vallejo-Cordoba, Belinda Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects |
title | Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects |
title_full | Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects |
title_fullStr | Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects |
title_full_unstemmed | Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects |
title_short | Fermented milks with specific Lactobacillus spp. with potential cardioprotective effects |
title_sort | fermented milks with specific lactobacillus spp. with potential cardioprotective effects |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122198/ https://www.ncbi.nlm.nih.gov/pubmed/37179799 http://dx.doi.org/10.1007/s13197-023-05715-1 |
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