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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/133699
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dc.contributor.authorCavallini, Daniela Cardoso Umbelino-
dc.contributor.authorSuzuki, Juliana Y.-
dc.contributor.authorAbdalla, Dulcinéia S P-
dc.contributor.authorVendramini, Regina C.-
dc.contributor.authorPauly-silveira, Nadiége D-
dc.contributor.authorRoselino, Mariana N-
dc.contributor.authorPinto, Roseli Ap.-
dc.contributor.authorRossi, Elizeu Antonio-
dc.date.accessioned2016-01-28T16:56:13Z-
dc.date.accessioned2016-10-25T21:28:41Z-
dc.date.available2016-01-28T16:56:13Z-
dc.date.available2016-10-25T21:28:41Z-
dc.date.issued2011-
dc.identifierhttp://link.springer.com/article/10.1186%2F1476-511X-10-126-
dc.identifier.citationLipids in health and disease, v. 10, n. 126, p. 1-9, 2011.-
dc.identifier.issn1476-511X-
dc.identifier.urihttp://hdl.handle.net/11449/133699-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/133699-
dc.description.abstractBackground: Previous work showed that daily ingestion of an aqueous soy extract fermented with Enterococcus faecium CRL 183 and Lactobacillus helveticus 416, supplemented or not with isoflavones, reduced the total cholesterol and non-HDL-cholesterol levels, increased the high-density lipoprotein (HDL) concentration and inhibited the raising of autoantibody against oxidized low-density lipoprotein (ox-LDL Ab) and the development of atherosclerotic lesions. Objective: The aim of this study was to characterize the fecal microbiota in order to investigate the possible correlation between fecal microbiota, serum lipid parameters and atherosclerotic lesion development in rabbits with induced hypercholesterolemia, that ingested the aqueous soy extract fermented with Enterococcus faecium CRL 183 and Lactobacillus helveticus 416. Methods: The rabbits were randomly allocated to five experimental groups (n = 6): control (C), hypercholesterolemic (H), hypercholesterolemic plus unfermented soy product (HUF), hypercholesterolemic plus fermented soy product (HF) and hypercholesterolemic plus isoflavone-supplemented fermented soy product (HIF). Lipid parameters and microbiota composition were analyzed on days 0 and 60 of the treatment and the atherosclerotic lesions were quantified at the end of the experiment. The fecal microbiota was characterized by enumerating the Lactobacillus spp., Bifidobacterium spp., Enterococcus spp., Enterobacteria and Clostridium spp. populations. Results: After 60 days of the experiment, intake of the probiotic soy product was correlated with significant increases (P < 0.05) on Lactobacillus spp., Bifidobacterium spp. and Enterococcus spp. and a decrease in the Enterobacteria population. A strong correlation was observed between microbiota composition and lipid profile. Populations of Enterococcus spp., Lactobacillus spp. and Bifidobacterium spp. were negatively correlated with total cholesterol, non-HDL-cholesterol, autoantibodies against oxidized LDL (oxLDL Ab) and lesion size. HDL-C levels were positively correlated with Lactobacillus spp., Bifidobacterium spp., and Enterococcus spp. populations. Conclusion: In conclusion, daily ingestion of the probiotic soy product, supplemented or not with isoflavones, may contribute to a beneficial balance of the fecal microbiota and this modulation is associated with an improved cholesterol profile and inhibition of atherosclerotic lesion development.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent1-9-
dc.language.isoeng-
dc.sourceCurrículo Lattes-
dc.subjectProbioticsen
dc.subjectEnterococcus faecium CRL 183en
dc.subjectFecal microbiotaen
dc.subjectLipid parametersen
dc.titleInfluence of a probiotic soy product on fecal microbiota and its association with cardiovascular risk factors in a animal modelen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationDepartment of Food and Nutrition, School of Pharmaceutical Sciences, Sao Paulo State University (UNESP), Araraquara, SP, Brazil-
dc.description.affiliationDepartment of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences, University of Sao Paulo (USP), Sao Paulo, Brazil-
dc.description.affiliationDepartment of Clinical Analysis, School of Pharmaceutical Sciences, Sao Paulo State University (UNESP) Araraquara, SP, Brazil-
dc.description.affiliationUnespDepartment of Food and Nutrition, School of Pharmaceutical Sciences, Sao Paulo State University (UNESP), Araraquara, SP, Brazil-
dc.description.affiliationUnespDepartment of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences, University of Sao Paulo (USP), Sao Paulo, Brazil-
dc.description.affiliationUnespDepartment of Clinical Analysis, School of Pharmaceutical Sciences, Sao Paulo State University (UNESP) Araraquara, SP, Brazil.-
dc.identifier.doi10.1186/1476-511X-10-126-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileISSN1476-511X-2011-10-126-1-9.pdf-
dc.relation.ispartofLipids in health and disease-
dc.identifier.lattes3242858535763793-
dc.identifier.lattes4631598241372861-
dc.identifier.lattes7605568238887469-
dc.identifier.lattes9905593337419625-
dc.identifier.lattes1194360710417891-
dc.identifier.lattes8546420799947783-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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