Esculin protects against methionine choline-deficient diet-induced non-alcoholic steatohepatitis by regulating the Sirt1/NF-
Alanine Transaminase
/ blood
Animals
Aspartate Aminotransferases
/ blood
Cell Survival
/ drug effects
Choline Deficiency
Cytokines
/ drug effects
Esculin
/ pharmacology
Fatty Acids, Nonesterified
Fibrosis
/ drug therapy
Hep G2 Cells
Hepatocytes
/ drug effects
Humans
Inflammation
/ drug therapy
Lipids
/ blood
Liver
/ drug effects
Male
Mice
Mice, Inbred C57BL
Models, Animal
NF-kappa B
/ metabolism
Non-alcoholic Fatty Liver Disease
/ chemically induced
RNA, Small Interfering
Signal Transduction
Silybin
/ pharmacology
Sirtuin 1
/ genetics
Inflammatory cytokine
acetylation of NF-κB p65
fibrosis
Journal
Pharmaceutical biology
ISSN: 1744-5116
Titre abrégé: Pharm Biol
Pays: England
ID NLM: 9812552
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
entrez:
10
7
2021
pubmed:
11
7
2021
medline:
22
12
2021
Statut:
ppublish
Résumé
Esculin, an active coumarin compound, has been demonstrated to exert anti-inflammatory effects. However, its potential role in non-alcoholic steatohepatitis (NASH) remains unclear. This study explored the hepatoprotective effect and the molecular mechanism of esculin in methionine choline-deficient (MCD) diet-induced NASH. Fifty C57BL/6J mice were divided into five groups: control, model, low dosage esculin (oral, 20 mg/kg), high dosage esculin (oral, 40 mg/kg), and silybin (oral, 105 mg/kg). All animals were fed a MCD diet, except those in the control group (control diet), for 6 weeks. Esculin (20 and 40 mg/kg) inhibited MCD diet-induced hepatic lipid content (triglyceride: 16.95 ± 0.67 and 14.85 ± 0.78 vs. 21.21 ± 1.13 mg/g; total cholesterol: 5.10 ± 0.34 and 4.08 ± 0.47 vs. 7.31 ± 0.58 mg/g), fibrosis, and inflammation (ALT: 379.61 ± 40.30 and 312.72 ± 21.45 vs. 559.51 ± 37.01 U/L; AST: 428.22 ± 34.29 and 328.23 ± 23.21 vs. 579.36 ± 31.93 U/L). These findings demonstrate that esculin ameliorates MCD diet-induced NASH by regulating the Sirt1/ac-NF-κB signalling pathway. Esculin could thus be employed as a therapy for NASH.
Identifiants
pubmed: 34243681
doi: 10.1080/13880209.2021.1945112
pmc: PMC8274538
doi:
Substances chimiques
Cytokines
0
Fatty Acids, Nonesterified
0
Lipids
0
NF-kappa B
0
RNA, Small Interfering
0
Esculin
1Y1L18LQAF
Silybin
4RKY41TBTF
Aspartate Aminotransferases
EC 2.6.1.1
Alanine Transaminase
EC 2.6.1.2
Sirtuin 1
EC 3.5.1.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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