Inflammatory gene expression analysis after prebiotic, probiotic and synbiotic supplementation in experimental nonalcoholic fatty liver disease
Carregando...
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
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-
Referências
- Abd El-Kader SM, 2015, WORLD J HEPATOL, V7, P846, DOI 10.4254/wjh.v7.i6.846
- Abu-Shanab A, 2010, NAT REV GASTRO HEPAT, V7, P691, DOI 10.1038/nrgastro.2010.172
- Valadez JMA, 2016, THER CLIN RISK MANAG, V12, P1729, DOI 10.2147/TCRM.S115902
- Alisi A, 2012, FRONT CELL INFECT MI, V2, DOI 10.3389/fcimb.2012.00132
- Alisi A, 2010, J PEDIATR GASTR NUTR, V50, P645, DOI 10.1097/MPG.0b013e3181c7bdf1
- Anand G, 2016, SEMIN LIVER DIS, V36, P37, DOI 10.1055/s-0035-1571276
- Arslan N, 2014, WORLD J GASTROENTERO, V20, P16452, DOI 10.3748/wjg.v20.i44.16452
- Bakhshimoghaddam F, 2018, J NUTR, V148, P1276, DOI 10.1093/jn/nxy088
- Baldwin AS, 1996, ANNU REV IMMUNOL, V14, P649, DOI 10.1146/annurev.immunol.14.1.649
- Bigorgne AE, 2016, PLOS ONE, V11, DOI 10.1371/journal.pone.0151063
- Bouhnik Y, 1997, J NUTR, V127, P444
- Capitan-Canadas F, 2014, MOL NUTR FOOD RES, V58, P1098, DOI 10.1002/mnfr.201300497
- Hernandez-Rodas MC, 2015, INT J MOL SCI, V16, P25168, DOI 10.3390/ijms161025168
- Cesaro C, 2011, DIGEST LIVER DIS, V43, P431, DOI 10.1016/j.dld.2010.10.015
- Chappuis E, 2017, MOLECULES, V22, DOI 10.3390/molecules22101725
- Compare D, 2012, NUTR METAB CARDIOVAS, V22, P471, DOI 10.1016/j.numecd.2012.02.007
- Delzenne NM, 2013, BRIT J NUTR, V109, pS81, DOI 10.1017/S0007114512004047
- Duseja A, 2014, CLIN LIVER DIS, V18, P59, DOI 10.1016/j.cld.2013.09.002
- Eslamparast T, 2014, AM J CLIN NUTR, V99, P535, DOI 10.3945/ajcn.113.068890
- Gratz SW, 2010, WORLD J GASTROENTERO, V16, P403, DOI 10.3748/wjg.v16.i4.403
- Hadi Amir, 2018, Crit Rev Food Sci Nutr, P1, DOI 10.1080/10408398.2018.1458021
- Henao-Mejia J, 2012, NATURE, V482, P179, DOI 10.1038/nature10809
- Iacono A, 2011, J NUTR BIOCHEM, V22, P699, DOI 10.1016/j.jnutbio.2010.10.002
- Ilan Y, 2012, WORLD J GASTROENTERO, V18, P2609, DOI 10.3748/wjg.v18.i21.2609
- John B, 2005, J IMMUNOL, V175, P1643, DOI 10.4049/jimmunol.175.3.1643
- Manzoni MSJ, 2008, EUR FOOD RES TECHNOL, V227, P1591, DOI 10.1007/s00217-008-0883-1
- Kapil S, 2016, WORLD J GASTROENTERO, V22, P9346, DOI 10.3748/wjg.v22.i42.9346
- Kawai T, 2006, CELL DEATH DIFFER, V13, P816, DOI 10.1038/sj.cdd.4401850
- Kok N, 1996, BRIT J NUTR, V76, P881, DOI 10.1079/BJN19960094
- Larkin TA, 2009, EUR J CLIN NUTR, V63, P238, DOI 10.1038/sj.ejcn.1602910
- Lawrence T, 2009, CSH PERSPECT BIOL, V1, DOI 10.1101/cshperspect.a001651
- Li DY, 2013, JPEN-PARENTER ENTER, V37, P787, DOI 10.1177/0148607113481623
- Li ZP, 2003, HEPATOLOGY, V37, P343, DOI 10.1053/jhep.2003.50048
- Lin P, 2015, PLOS ONE, V10, DOI 10.1371/journal.pone.0140346
- Loomba R, 2017, CELL METAB, V25, P1054, DOI 10.1016/j.cmet.2017.04.001
- Ma YY, 2013, WORLD J GASTROENTERO, V19, P6911, DOI 10.3748/wjg.v19.i40.6911
- Mehal WZ, 2013, NAT REV GASTRO HEPAT, V10, P637, DOI 10.1038/nrgastro.2013.146
- Miura K, 2014, WORLD J GASTROENTERO, V20, P7381, DOI 10.3748/wjg.v20.i23.7381
- Mofidi F, 2017, BRIT J NUTR, V117, P662, DOI 10.1017/S0007114517000204
- Mogensen TH, 2009, CLIN MICROBIOL REV, V22, P240, DOI 10.1128/CMR.00046-08
- Muzio M, 2000, J IMMUNOL, V164, P5998, DOI 10.4049/jimmunol.164.11.5998
- Parnell JA, 2012, LIVER INT, V32, P701, DOI 10.1111/j.1478-3231.2011.02730.x
- Paschos P, 2009, HIPPOKRATIA, V13, P9
- Pfaffl MW, 2001, NUCLEIC ACIDS RES, V29, DOI 10.1093/nar/29.9.e45
- Reeves PG, 1997, J NUTR, V127, pS838
- Saberi M, 2009, CELL METAB, V10, P419, DOI 10.1016/j.cmet.2009.09.006
- Sakaguchi S, 2011, DRUG METAB PHARMACOK, V26, P30, DOI 10.2133/dmpk.DMPK-10-RV-087
- Son G, 2010, GASTROENT RES PRACT, DOI 10.1155/2010/453563
- Sumida Y, 2018, J GASTROENTEROL, V53, P362, DOI 10.1007/s00535-017-1415-1
- Targher G, 2017, NAT REV NEPHROL, V13, P297, DOI 10.1038/nrneph.2017.16
- TOBIAS PS, 1995, J BIOL CHEM, V270, P10482, DOI 10.1074/jbc.270.18.10482
- Younossi ZM, 2016, HEPATOLOGY, V64, P73, DOI 10.1002/hep.28431
- Zhang X, 2018, PROTEIN CELL, V9, P164, DOI 10.1007/s13238-017-0436-0