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PMID: 22749137 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Lactobacillus casei Shirota protects from fructose-induced liver steatosis: a mouse model.

The Journal of nutritional biochemistry ·Vol. 24 ·No. 3 ·2013-03-00 ·Pages 531-8

Wagnerberger S, Spruss A, Kanuri G, Stahl C, Schröder M, Vetter W, Bischoff SC, Bergheim I

Abstract

To test the hypothesis that Lactobacillus casei Shirota (Lcs) protects against the onset of non-alcoholic fatty liver disease (NAFLD) in a mouse model of fructose-induced steatosis, C57BL/6J mice were either fed tap water or 30% fructose solution +/- Lcs for 8 weeks. Chronic consumption of 30% fructose solution led to a significant increase in hepatic steatosis as well as plasma alanine-aminotransferase (ALT) levels, which was attenuated by treatment with Lcs. Protein levels of the tight junction protein occludin were found to be markedly lower in both fructose treated groups in the duodenum, whereas microbiota composition in this part of the intestine was not affected. Lcs treatment markedly attenuated the activation of the Toll-like receptor (TLR) 4 signalling cascade found in the livers of mice only treated with fructose. Moreover, in livers of fructose fed mice treated with Lcs peroxisome proliferator-activated receptor (PPAR)-γ activity was markedly higher than in mice only fed fructose. Taken together, the results of the present study suggest that the dietary intake of Lcs protects against the onset of fructose-induced NAFLD through mechanisms involving an attenuation of the TLR-4-signalling cascade in the liver.

MeSH Terms
Alanine Transaminase/analysis,metabolism Animals Butyrates/blood Cell Line Cell Proliferation Chromans/agonists,pharmacology DNA Fingerprinting DNA, Bacterial/genetics,isolation & purification Disease Models, Animal Fatty Liver/chemically induced,pathology,prevention & control Fructose/adverse effects Hypoglycemic Agents/agonists,pharmacology Intestinal Mucosa/metabolism Intestines/drug effects Lactobacillus casei/genetics,metabolism Liver/drug effects,metabolism Mice Mice, Inbred C57BL Non-alcoholic Fatty Liver Disease PPAR gamma/genetics,metabolism Sequence Analysis, DNA Signal Transduction Thiazolidinediones/agonists,pharmacology Toll-Like Receptor 4/genetics,metabolism Troglitazone Up-Regulation
Chemicals
Butyrates Chromans DNA, Bacterial Hypoglycemic Agents PPAR gamma Thiazolidinediones Tlr4 protein, mouse Toll-Like Receptor 4 Fructose Alanine Transaminase Troglitazone
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Wagnerberger Sabine
Department of Nutritional Medicine-180 a, University of Hohenheim, Fruwirthstrasse 12, 70599 Stuttgart, Germany.
Spruss Astrid
Kanuri Giridhar
Stahl Carolin
Schröder Markus
Vetter Walter
Bischoff Stephan C
Bergheim Ina
Article Info
Journal
The Journal of nutritional biochemistry
Abbr.
J Nutr Biochem
ISSN
1873-4847
Published
2013-03-00
Epub
2012-00-27
Pages
531-8
Language
English
Region
United States
NLM ID
9010081
Subset
IM
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