» Articles » PMID: 36698477

ZJUIDS14 Alleviates Non-alcoholic Fatty Liver Disease in Mice in Association with Modulation in the Gut Microbiota

Overview
Journal Front Nutr
Date 2023 Jan 26
PMID 36698477
Authors
Affiliations
Soon will be listed here.
Abstract

This present study was designed to explore the protective role of ZJUIDS14 against Non-alcoholic Fatty Liver Disease (NAFLD) in a high-fat-diet (HFD)-induced C57BL/6 mice model. The probiotic (10 CFU/every other day) was administered by oral gavage for 12 weeks. We found that ZJUIDS14 intervention significantly alleviated HFD related hepatic steatosis, liver damage, insulin resistance, and increased hepatic expression of peroxisome proliferator activated receptor α (PPAR-α) while stimulating the activation of AMP-activated protein kinase (AMPK). Furthermore, ZJUIDS14 improved mitochondrial function as reflected by an increase in dynamin related protein 1 (DRP1) and a decrease of proteins associated with oxidative phosphorylation (OXPHOS) after the treatment. Additionally, mice from the ZJUIDS14 group had a restored intestinal flora and homeostasis involving , -, , , and . Meanwhile, these five genera exhibited a significant (negative or positive) association with ileum inflammation mRNA levels and SCFA contents, by Spearman's correlation analysis. In general, our data demonstrated that ZJUIDS14 mitigates hepatic steatosis and liver damage induced by HFD. Specifically, they strengthened the integrity of the intestinal barrier, regulated gut microbiota, and improved mitochondrial function. Our data provide an experimental basis for ZJUIDS14 as a promising candidate to prevent NAFLD.

Citing Articles

Gut microbiota modulation via fecal microbiota transplantation mitigates hyperoxaluria and calcium oxalate crystal depositions induced by high oxalate diet.

An L, Li S, Chang Z, Lei M, He Z, Xu P Gut Microbes. 2025; 17(1):2457490.

PMID: 39873191 PMC: 11776474. DOI: 10.1080/19490976.2025.2457490.


Key Taxa of the Gut Microbiome Associated with the Relationship Between Environmental Sensitivity and Inflammation-Related Biomarkers.

Takasugi S, Iimura S, Yasuda M, Saito Y, Morifuji M Microorganisms. 2025; 13(1).

PMID: 39858953 PMC: 11767568. DOI: 10.3390/microorganisms13010185.


The role of intestinal flora in metabolic dysfunction-associated steatotic liver disease and treatment strategies.

Wang L, Sun J, Chen S, Sun Y, Zheng Y, Feng J Front Med (Lausanne). 2025; 11():1490929.

PMID: 39839647 PMC: 11746088. DOI: 10.3389/fmed.2024.1490929.


Probiotics and Non-Alcoholic Fatty Liver Disease: Unveiling the Mechanisms of and in Modulating Lipid Metabolism, Inflammation, and Intestinal Barrier Integrity.

Lu J, Shataer D, Yan H, Dong X, Zhang M, Qin Y Foods. 2024; 13(18).

PMID: 39335920 PMC: 11431124. DOI: 10.3390/foods13182992.


Identification of immune-associated genes with altered expression in the spleen of mice enriched with probiotic Lactobacillus species using RNA-seq profiling.

Truong A, Tran H, Chu N, Phan L, Phan H, Dang T Anim Biosci. 2024; 38(2):336-349.

PMID: 39210803 PMC: 11725755. DOI: 10.5713/ab.24.0280.


References
1.
Lantier L, Fentz J, Mounier R, Leclerc J, Treebak J, Pehmoller C . AMPK controls exercise endurance, mitochondrial oxidative capacity, and skeletal muscle integrity. FASEB J. 2014; 28(7):3211-24. DOI: 10.1096/fj.14-250449. View

2.
Huang J, Jia Y, Fu T, Viswakarma N, Bai L, Rao M . Sustained activation of PPARα by endogenous ligands increases hepatic fatty acid oxidation and prevents obesity in ob/ob mice. FASEB J. 2011; 26(2):628-38. PMC: 3290446. DOI: 10.1096/fj.11-194019. View

3.
Liu H, Niu Q, Wang T, Dong H, Bian C . Lipotoxic hepatocytes promote nonalcoholic fatty liver disease progression by delivering microRNA-9-5p and activating macrophages. Int J Biol Sci. 2022; 17(14):3745-3759. PMC: 8898344. DOI: 10.7150/ijbs.57610. View

4.
Li Q, Tan J, He Y, Bai F, Li S, Hou Y . Atractylenolide III ameliorates Non-Alcoholic Fatty Liver Disease by activating Hepatic Adiponectin Receptor 1-Mediated AMPK Pathway. Int J Biol Sci. 2022; 18(4):1594-1611. PMC: 8898375. DOI: 10.7150/ijbs.68873. View

5.
Liang W, Enee E, Andre-Vallee C, Falcone M, Sun J, Diana J . Intestinal Cathelicidin Antimicrobial Peptide Shapes a Protective Neonatal Gut Microbiota Against Pancreatic Autoimmunity. Gastroenterology. 2022; 162(4):1288-1302.e16. DOI: 10.1053/j.gastro.2021.12.272. View