Oral Supplementation of Sodium Butyrate Attenuates the Progression of Non-Alcoholic Steatohepatitis.
Animals
Butyric Acid
/ administration & dosage
Cholesterol, Dietary
/ adverse effects
Diet, High-Fat
/ adverse effects
Dietary Supplements
Disease Models, Animal
Disease Progression
Female
Glucose
/ metabolism
Inflammation
Interleukin-6
/ metabolism
Intestine, Small
/ metabolism
Liver
/ metabolism
Melatonin
/ metabolism
Mice, Inbred C57BL
Nitric Oxide Synthase Type II
/ metabolism
Non-alcoholic Fatty Liver Disease
/ drug therapy
Toll-Like Receptor 4
/ metabolism
Tumor Necrosis Factor-alpha
/ metabolism
inducible nitric oxide synthase
melatonin synthesis
non-alcoholic steatohepatitis
sodium butyrate
toll-like receptor 4
Journal
Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595
Informations de publication
Date de publication:
30 Mar 2020
30 Mar 2020
Historique:
received:
20
02
2020
revised:
23
03
2020
accepted:
27
03
2020
entrez:
3
4
2020
pubmed:
3
4
2020
medline:
29
12
2020
Statut:
epublish
Résumé
Sodium butyrate (SoB) supplementation has been suggested to attenuate the development of non-alcoholic fatty liver disease (NAFLD). Here, we determined the therapeutic potential of SoB on NAFLD progression and molecular mechanism involved. Eight-week old C57BL/6J mice were pair-fed a fat-, fructose- and cholesterol-rich diet (FFC) or control diet (C). After 8 weeks, some mice received 0.6g SoB/kg bw in their respective diets (C+SoB; FFC+SoB) or were maintained on C or FFC for the next 5 weeks of feeding. Liver damage, markers of glucose metabolism, inflammation, intestinal barrier function and melatonin metabolism were determined. FFC-fed mice progressed from simple steatosis to early non-alcoholic steatohepatitis, along with significantly higher TNFα and IL-6 protein levels in the liver and impaired glucose tolerance. In FFC+SoB-fed mice, disease was limited to steatosis associated with protection against the induction of
Identifiants
pubmed: 32235497
pii: nu12040951
doi: 10.3390/nu12040951
pmc: PMC7231312
pii:
doi:
Substances chimiques
Cholesterol, Dietary
0
Interleukin-6
0
Tlr4 protein, mouse
0
Toll-Like Receptor 4
0
Tumor Necrosis Factor-alpha
0
Butyric Acid
107-92-6
Nitric Oxide Synthase Type II
EC 1.14.13.39
Nos2 protein, mouse
EC 1.14.13.39
Glucose
IY9XDZ35W2
Melatonin
JL5DK93RCL
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Bundesministerium für Bildung und Forschung
ID : FKZ: 01EA1305 to I.B.
Déclaration de conflit d'intérêts
The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
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