Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver

Detalhes bibliográficos
Autor(a) principal: Alves, Claudia Cristina [UNIFESP]
Data de Publicação: 2017
Outros Autores: Waitzberg, Dan Linetzky, Andrade, Laila Santos de [UNIFESP], Aguiar, Lais dos Santos [UNIFESP], Reis, Milene Barcelos [UNIFESP], Guanabara, Camila Chaves [UNIFESP], Aguiar, Odair [UNIFESP], Ribeiro, Daniel Araki [UNIFESP], Sala, Priscila
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://repositorio.unifesp.br/handle/11600/57139
https://dx.doi.org/10.3389/fmicb.2017.02010
Resumo: Background and aims: Non-alcoholic fatty liver disease (NAFLD) is characterized by the presence of fat in hepatocytes because of decreased β-oxidation and increased lipogenesis. Prebiotics, probiotics, and synbiotic have modulatory effects on intestinal microbiota and may influence the gut-liver axis. Our aim was to evaluate the effects of prebiotic, probiotics, and synbiotic on liver histopathology and gene expression related to β-oxidation and lipogenesis after hypercholesterolemia. Methods: Wistar male adult rats (n = 40) were submitted to hypercholesterolemic conditions (HPC) (60 days). On Day 30 of HPC, rats were subdivided in 5 groups: negative control (NC): without HPC + Gv (distilled water); positive control (PC): with HPC + Gv (distilled water); prebiotic (PRE): HPC + Gv with prebiotic (Fiber FOS®); probiotic (PRO): HPC + Gv with probiotic strains Gv (Probiatop®); and synbiotic (SYN): HPC + Gv with synbiotic (Simbioflora®). All rats were sacrificed on Day 30 post-treatment. Blood was collected to verify total serum cholesterol, and liver tissue was sampled to verify histopathological changes and gene expression. Gene expression related to ß-oxidation (PPAR-α and CPT-1) and lipogenesis (SREBP-1c, FAS and ME) was evaluated in liver tissue using RT-qPCR. Results: PC had higher cholesterol levels when compared to NC. PRE and SYN rats had lower cholesterol levels than PC. PC rats showed more histopathological changes than NC rats; PRE and SYN rats showed fewer alterations than PC rats. PPAR-α was expressed at higher levels in SYN and PC rats compared with PRE and PRO rats. CPT-1 expression was similar in all groups. SREBP-1c was expressed at higher levels in PC rats compared with NC rats; levels were lower in SYN rats compared with PRO rats; levels were lower in PRE rats compared with PC and PRO rats. FAS was expressed at lower levels in PRE rats compared with SYN rats. ME expression was lower in PC rats compared with NC rats. Conclusion: Prebiotic and synbiotic supplementation improve hepatic alterations related to hypercholesterolemia. These changes appear to be mediated by altered expression of genes related to β-oxidation and lipogenesis.
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spelling Alves, Claudia Cristina [UNIFESP]Waitzberg, Dan LinetzkyAndrade, Laila Santos de [UNIFESP]Aguiar, Lais dos Santos [UNIFESP]Reis, Milene Barcelos [UNIFESP]Guanabara, Camila Chaves [UNIFESP]Aguiar, Odair [UNIFESP]Ribeiro, Daniel Araki [UNIFESP]Sala, Priscila2020-08-04T13:39:49Z2020-08-04T13:39:49Z2017Frontiers In Microbiology. Lausanne, v. 8, p. -, 2017.1664-302Xhttps://repositorio.unifesp.br/handle/11600/57139https://dx.doi.org/10.3389/fmicb.2017.02010WOS000413105800001.pdf10.3389/fmicb.2017.02010WOS:000413105800001Background and aims: Non-alcoholic fatty liver disease (NAFLD) is characterized by the presence of fat in hepatocytes because of decreased β-oxidation and increased lipogenesis. Prebiotics, probiotics, and synbiotic have modulatory effects on intestinal microbiota and may influence the gut-liver axis. Our aim was to evaluate the effects of prebiotic, probiotics, and synbiotic on liver histopathology and gene expression related to β-oxidation and lipogenesis after hypercholesterolemia. Methods: Wistar male adult rats (n = 40) were submitted to hypercholesterolemic conditions (HPC) (60 days). On Day 30 of HPC, rats were subdivided in 5 groups: negative control (NC): without HPC + Gv (distilled water); positive control (PC): with HPC + Gv (distilled water); prebiotic (PRE): HPC + Gv with prebiotic (Fiber FOS®); probiotic (PRO): HPC + Gv with probiotic strains Gv (Probiatop®); and synbiotic (SYN): HPC + Gv with synbiotic (Simbioflora®). All rats were sacrificed on Day 30 post-treatment. Blood was collected to verify total serum cholesterol, and liver tissue was sampled to verify histopathological changes and gene expression. Gene expression related to ß-oxidation (PPAR-α and CPT-1) and lipogenesis (SREBP-1c, FAS and ME) was evaluated in liver tissue using RT-qPCR. Results: PC had higher cholesterol levels when compared to NC. PRE and SYN rats had lower cholesterol levels than PC. PC rats showed more histopathological changes than NC rats; PRE and SYN rats showed fewer alterations than PC rats. PPAR-α was expressed at higher levels in SYN and PC rats compared with PRE and PRO rats. CPT-1 expression was similar in all groups. SREBP-1c was expressed at higher levels in PC rats compared with NC rats; levels were lower in SYN rats compared with PRO rats; levels were lower in PRE rats compared with PC and PRO rats. FAS was expressed at lower levels in PRE rats compared with SYN rats. ME expression was lower in PC rats compared with NC rats. Conclusion: Prebiotic and synbiotic supplementation improve hepatic alterations related to hypercholesterolemia. These changes appear to be mediated by altered expression of genes related to β-oxidation and lipogenesis.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ Fed Sao Paulo, Dept Biosci, Santos, BrazilUniv Sao Paulo, Dept Gastroenterol, Sch Med, Sao Paulo, BrazilUniv Fed Sao Paulo, Nutr Grad, Santos, BrazilUniv Fed Sao Paulo, Dept Biosci, Santos, BrazilUniv Fed Sao Paulo, Nutr Grad, Santos, BrazilFAPESP: 2011/50289-1Web of Science-engFrontiers Media SaFrontiers In MicrobiologyCholesterol dietSteatosisRatsPrebioticProbioticSynbioticGene expressionPrebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liverinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleLausanne8info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000413105800001.pdfapplication/pdf1075533${dspace.ui.url}/bitstream/11600/57139/1/WOS000413105800001.pdf5add3722f8ae0fc8a8e143c579171316MD51open accessTEXTWOS000413105800001.pdf.txtWOS000413105800001.pdf.txtExtracted texttext/plain46589${dspace.ui.url}/bitstream/11600/57139/5/WOS000413105800001.pdf.txt2ad233c73da95e9931346daac4ae863bMD55open accessTHUMBNAILWOS000413105800001.pdf.jpgWOS000413105800001.pdf.jpgIM Thumbnailimage/jpeg7536${dspace.ui.url}/bitstream/11600/57139/7/WOS000413105800001.pdf.jpg5feeced93d3f4ed587cacbe0134cf2f8MD57open access11600/571392023-06-05 19:13:53.256open accessoai:repositorio.unifesp.br:11600/57139Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-06-05T22:13:53Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
title Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
spellingShingle Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
Alves, Claudia Cristina [UNIFESP]
Cholesterol diet
Steatosis
Rats
Prebiotic
Probiotic
Synbiotic
Gene expression
title_short Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
title_full Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
title_fullStr Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
title_full_unstemmed Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
title_sort Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver
author Alves, Claudia Cristina [UNIFESP]
author_facet Alves, Claudia Cristina [UNIFESP]
Waitzberg, Dan Linetzky
Andrade, Laila Santos de [UNIFESP]
Aguiar, Lais dos Santos [UNIFESP]
Reis, Milene Barcelos [UNIFESP]
Guanabara, Camila Chaves [UNIFESP]
Aguiar, Odair [UNIFESP]
Ribeiro, Daniel Araki [UNIFESP]
Sala, Priscila
author_role author
author2 Waitzberg, Dan Linetzky
Andrade, Laila Santos de [UNIFESP]
Aguiar, Lais dos Santos [UNIFESP]
Reis, Milene Barcelos [UNIFESP]
Guanabara, Camila Chaves [UNIFESP]
Aguiar, Odair [UNIFESP]
Ribeiro, Daniel Araki [UNIFESP]
Sala, Priscila
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Alves, Claudia Cristina [UNIFESP]
Waitzberg, Dan Linetzky
Andrade, Laila Santos de [UNIFESP]
Aguiar, Lais dos Santos [UNIFESP]
Reis, Milene Barcelos [UNIFESP]
Guanabara, Camila Chaves [UNIFESP]
Aguiar, Odair [UNIFESP]
Ribeiro, Daniel Araki [UNIFESP]
Sala, Priscila
dc.subject.eng.fl_str_mv Cholesterol diet
Steatosis
Rats
Prebiotic
Probiotic
Synbiotic
Gene expression
topic Cholesterol diet
Steatosis
Rats
Prebiotic
Probiotic
Synbiotic
Gene expression
description Background and aims: Non-alcoholic fatty liver disease (NAFLD) is characterized by the presence of fat in hepatocytes because of decreased β-oxidation and increased lipogenesis. Prebiotics, probiotics, and synbiotic have modulatory effects on intestinal microbiota and may influence the gut-liver axis. Our aim was to evaluate the effects of prebiotic, probiotics, and synbiotic on liver histopathology and gene expression related to β-oxidation and lipogenesis after hypercholesterolemia. Methods: Wistar male adult rats (n = 40) were submitted to hypercholesterolemic conditions (HPC) (60 days). On Day 30 of HPC, rats were subdivided in 5 groups: negative control (NC): without HPC + Gv (distilled water); positive control (PC): with HPC + Gv (distilled water); prebiotic (PRE): HPC + Gv with prebiotic (Fiber FOS®); probiotic (PRO): HPC + Gv with probiotic strains Gv (Probiatop®); and synbiotic (SYN): HPC + Gv with synbiotic (Simbioflora®). All rats were sacrificed on Day 30 post-treatment. Blood was collected to verify total serum cholesterol, and liver tissue was sampled to verify histopathological changes and gene expression. Gene expression related to ß-oxidation (PPAR-α and CPT-1) and lipogenesis (SREBP-1c, FAS and ME) was evaluated in liver tissue using RT-qPCR. Results: PC had higher cholesterol levels when compared to NC. PRE and SYN rats had lower cholesterol levels than PC. PC rats showed more histopathological changes than NC rats; PRE and SYN rats showed fewer alterations than PC rats. PPAR-α was expressed at higher levels in SYN and PC rats compared with PRE and PRO rats. CPT-1 expression was similar in all groups. SREBP-1c was expressed at higher levels in PC rats compared with NC rats; levels were lower in SYN rats compared with PRO rats; levels were lower in PRE rats compared with PC and PRO rats. FAS was expressed at lower levels in PRE rats compared with SYN rats. ME expression was lower in PC rats compared with NC rats. Conclusion: Prebiotic and synbiotic supplementation improve hepatic alterations related to hypercholesterolemia. These changes appear to be mediated by altered expression of genes related to β-oxidation and lipogenesis.
publishDate 2017
dc.date.issued.fl_str_mv 2017
dc.date.accessioned.fl_str_mv 2020-08-04T13:39:49Z
dc.date.available.fl_str_mv 2020-08-04T13:39:49Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.citation.fl_str_mv Frontiers In Microbiology. Lausanne, v. 8, p. -, 2017.
dc.identifier.uri.fl_str_mv https://repositorio.unifesp.br/handle/11600/57139
https://dx.doi.org/10.3389/fmicb.2017.02010
dc.identifier.issn.none.fl_str_mv 1664-302X
dc.identifier.file.none.fl_str_mv WOS000413105800001.pdf
dc.identifier.doi.none.fl_str_mv 10.3389/fmicb.2017.02010
dc.identifier.wos.none.fl_str_mv WOS:000413105800001
identifier_str_mv Frontiers In Microbiology. Lausanne, v. 8, p. -, 2017.
1664-302X
WOS000413105800001.pdf
10.3389/fmicb.2017.02010
WOS:000413105800001
url https://repositorio.unifesp.br/handle/11600/57139
https://dx.doi.org/10.3389/fmicb.2017.02010
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language eng
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dc.coverage.none.fl_str_mv Lausanne
dc.publisher.none.fl_str_mv Frontiers Media Sa
publisher.none.fl_str_mv Frontiers Media Sa
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instname:Universidade Federal de São Paulo (UNIFESP)
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reponame_str Repositório Institucional da UNIFESP
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