Esculin protects against methionine choline-deficient diet-induced non-alcoholic steatohepatitis by regulating the Sirt1/NF-


Journal

Pharmaceutical biology
ISSN: 1744-5116
Titre abrégé: Pharm Biol
Pays: England
ID NLM: 9812552

Informations de publication

Date de publication:
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

922-932

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Auteurs

Xi-Ding Yang (XD)

Department of Pharmacy, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Hunan Provincial Engineering Research Central of Translational Medical and Innovative Drug, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.

Zhuo Chen (Z)

Department of Geriatrics, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.

Ling Ye (L)

Department of Geriatrics, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.

Jing Chen (J)

Department of Pharmacology, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan, China.

Yong-Yu Yang (YY)

Department of Pharmacy, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Hunan Provincial Engineering Research Central of Translational Medical and Innovative Drug, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.

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Classifications MeSH