Inflammatory gene expression analysis after prebiotic, probiotic and synbiotic supplementation in experimental nonalcoholic fatty liver disease

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Citações na Scopus
3
Tipo de produção
article
Data de publicação
2019
Título da Revista
ISSN da Revista
Título do Volume
Editora
EMERALD GROUP PUBLISHING LTD
Autores
RIBEIRO, Daniel Araki
FERREIRA, Jessica Almeida da Cruz
AGUIAR, Odair
ALVES, Claudia Cristina
Citação
NUTRITION & FOOD SCIENCE, v.49, n.1, p.75-84, 2019
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Purpose The purpose of this study is to evaluate the effects of prebiotic, probiotic and synbiotic supplementation on liver histopathology and TLR-4, NF kappa B and TNF-alpha gene expression involved in the inflammatory cascade and pathogenesis of experimental nonalcoholic fatty liver disease (NAFLD). Design/methodology/approach Wistar male adult rats (n = 40) were submitted to hypercholesterolemic conditions (60 days). On Day 30 of hypercholesterolemic conditions, rats were subdivided in five groups: negative control (NC), positive control (PC), prebiotic (PRE), probiotic (PRO) and synbiotic (SYN). All rats were sacrificed on Day 60. Liver tissue was used to verify histopathological changes and gene expression. Gene expression of TLR-4, TNF-alpha and NF kappa B was evaluated in liver tissue using RT-qPCR. Findings Histopathological analysis: PC showed more changes than NC, and PRE and SYN showed fewer alterations than PC. Gene expression analysis: PRE showed higher TLR-4, and NF kappa B and TNF-alpha compared to PC. Also, PRE showed higher TLR-4 when compared to PRO and SYN. SYN group revealed higher TLR-4 and NF kappa B expressions compared to PC. PRO group also showed higher NF kappa B expression compared to PC. Originality/value NAFLD is a significant health concern, and it found that prebiotic, probiotic and synbiotic supplementation could have positive effects as a nonpharmacological approach to control this disease.
Palavras-chave
Probiotic, NFkB, Nonalcoholic fatty liver disease, Prebiotic, TLR-4, TNF-
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