» Articles » PMID: 39046973

Probiotic Lactobacillus Fermentum TSF331, Lactobacillus Reuteri TSR332, and Lactobacillus Plantarum TSP05 Improved Liver Function and Uric Acid Management-A Pilot Study

Overview
Journal PLoS One
Date 2024 Jul 24
PMID 39046973
Authors
Affiliations
Soon will be listed here.
Abstract

Metabolic-associated fatty liver disease (MAFLD) is predominantly associated with metabolic disturbances representing aberrant liver function and increased uric acid (UA) levels. Growing evidences have suggested a close relationship between metabolic disturbances and the gut microbiota. A placebo-controlled, double-blinded, randomized clinical trial was therefore conducted to explore the impacts of daily supplements with various combinations of the probiotics, Lactobacillus fermentum TSF331, Lactobacillus reuteri TSR332, and Lactobacillus plantarum TSP05 with a focus on liver function and serum UA levels. Test subjects with abnormal levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and UA were recruited and randomly allocated into six groups. Eighty-two participants successfully completed the 60-day intervention without any dropouts or occurrence of adverse events. The serum AST, ALT, and UA levels were significantly reduced in all treatment groups (P < 0.05). The fecal microbiota analysis revealed the intervention led to an increase in the population of commensal bacteria and a decrease in pathobiont bacteria, especially Bilophila wadsworthia. The in vitro study indicated the probiotic treatments reduced lipid accumulation and inflammatory factor expressions in HepG2 cells, and also promoted UA excretion in Caco-2 cells. The supplementation of multi-strain probiotics (TSF331, TSR332, and TSP05) together can improve liver function and UA management and may have good potential in treating asymptomatic MAFLD. Trial registration. The trial was registered in the US Library of Medicine (clinicaltrials.gov) with the number NCT06183801 on December 28, 2023.

Citing Articles

Characterization of Human Breast Milk-Derived MBHC 10138 with Respect to Purine Degradation, Anti-Biofilm, and Anti-Lipid Accumulation Activities.

Cheng J, Cho J, Suh J Antibiotics (Basel). 2024; 13(10).

PMID: 39452230 PMC: 11504937. DOI: 10.3390/antibiotics13100964.

References
1.
Kanmani P, Kim H . Protective Effects of Lactic Acid Bacteria Against TLR4 Induced Inflammatory Response in Hepatoma HepG2 Cells Through Modulation of Toll-Like Receptor Negative Regulators of Mitogen-Activated Protein Kinase and NF-κB Signaling. Front Immunol. 2018; 9:1537. PMC: 6039550. DOI: 10.3389/fimmu.2018.01537. View

2.
Lima W, Martins-Santos M, Chaves V . Uric acid as a modulator of glucose and lipid metabolism. Biochimie. 2015; 116:17-23. DOI: 10.1016/j.biochi.2015.06.025. View

3.
Musazadeh V, Roshanravan N, Dehghan P, Ahrabi S . Effect of Probiotics on Liver Enzymes in Patients With Non-alcoholic Fatty Liver Disease: An Umbrella of Systematic Review and Meta-Analysis. Front Nutr. 2022; 9:844242. PMC: 9169800. DOI: 10.3389/fnut.2022.844242. View

4.
Zou Y, Ro K, Jiang C, Yin D, Zhao L, Zhang D . The anti-hyperuricemic and gut microbiota regulatory effects of a novel purine assimilatory strain, Lactiplantibacillus plantarum X7022. Eur J Nutr. 2023; 63(3):697-711. DOI: 10.1007/s00394-023-03291-w. View

5.
Toshikuni N, Tsutsumi M, Arisawa T . Clinical differences between alcoholic liver disease and nonalcoholic fatty liver disease. World J Gastroenterol. 2014; 20(26):8393-406. PMC: 4093692. DOI: 10.3748/wjg.v20.i26.8393. View