Functional Probiotic Characterization and In Vivo Cholesterol-Lowering Activity of Lactobacillus helveticus Isolated from Fermented Cow Milk
We characterized the probiotic properties of strains KII13 and KHI1 isolated from fermented cow milk by in vitro and in vivo studies. The strains exhibited tolerance to simulated orogastrointestinal condition, adherence to Caco-2 cells, and antimicrobial activity. Both strains produced bioactive tri...
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Veröffentlicht in: | Journal of microbiology and biotechnology 2016, 26(10), , pp.1675-1686 |
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Sprache: | eng |
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Zusammenfassung: | We characterized the probiotic properties of
strains KII13 and KHI1 isolated from fermented cow milk by in vitro and in vivo studies. The strains exhibited tolerance to simulated orogastrointestinal condition, adherence to Caco-2 cells, and antimicrobial activity. Both
strains produced bioactive tripeptides, isoleucylprolyl-proline and valyl-prolyl-proline, during fermentation of milk. KII13 showed higher in vitro cholesterol-lowering activity (47%) compared with KHI1 (28%) and
ATCC 15009 (22%), and hence, it was selected for in vivo study of cholesterol-lowering activity in atherogenic diet-fed hypercholesterolemic mice. For the study, mice were divided into four groups (
., normal diet control group, atherogenic diet control group (HCD), KII13- atherogenic diet group (HCD-KII13), and
ATCC 43121-atherogenic diet group (HCD-
) as positive control). The serum total cholesterol level was significantly decreased by 8.6% and 7.78% in the HCD-KII13 and HCD-
groups (
< 0.05), respectively, compared with the HCD group. Low-density lipoprotein cholesterol levels in both HCD-KII13 and HCD-
groups were decreased by 13% and 11%, respectively, compared with the HCD group (both,
< 0.05). Analysis of cholesterol metabolism-related gene expression in mice liver showed increased expression of
and
genes in mice fed with KII13. By comparing all the results, we conclude that
KII13 could be used as a potential probiotic strain to produce antihypertensive peptides and reduce serum cholesterol. |
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ISSN: | 1017-7825 1738-8872 |
DOI: | 10.4014/jmb.1603.03005 |