» Articles » PMID: 32267892

A Combination of Monosodium Glutamate and High-fat and High-fructose Diets Increases the Risk of Kidney Injury, Gut Dysbiosis and Host-microbial Co-metabolism

Overview
Journal PLoS One
Date 2020 Apr 9
PMID 32267892
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Consumption of either monosodium glutamate (MSG) or high-fat and high-fructose (HFF) diets changes the gut microbiome and hence contributes to development of several diseases. In this study, with an emphasis on kidney injury, hamsters were divided into 4 groups as follows: (1) hamsters fed with standard diet (control); (2) hamsters fed with standard diet and MSG in drinking water (MSG); (3) hamsters fed with high-fat and high-fructose diets (HFF), and (4) animals fed MSG+HFF. After 8 months, the animals were used for the study. Despite showing normal kidney function, hamsters fed with MSG+HFF exhibited signs of kidney damage as demonstrated by the highest expression levels of high-mobility group box-1 and kidney injury molecule-1 in kidney tissues, while slight changes of histopathological features in H&E-stained sections and normal levels of creatinine were observed, indicating possible early stages of kidney injury. Sequencing of the microbial 16S rRNA gene revealed that animals fed with the MSG+HFF diet had a higher ratio of gut Firmicutes/Bacteroidetes along with marked changes in abundance and diversity of gut microbiome compared to hamsters fed with MSG or HFF alone. In addition, 1H Nuclear magnetic resonance spectroscopy showed an elevation of urine p-cresol sulfate levels in the MSG+HFF group. These results indicate that consumption of both MSG and HFF increases the risk of kidney injury, induces gut dysbiosis and an increase in the amount of p-cresol sulfate in hamsters.

Citing Articles

Association between monosodium glutamate consumption with changes in gut microbiota and related metabolic dysbiosis-A systematic review.

Ahangari H, Bahramian B, Khezerlou A, Tavassoli M, Kiani-Salmi N, Tarhriz V Food Sci Nutr. 2024; 12(8):5285-5295.

PMID: 39139924 PMC: 11317663. DOI: 10.1002/fsn3.4198.


Metagenomics and metaproteomics alterations are associated with kidney disease in opisthorchiasis hamsters fed a high-fat and high-fructose diet.

Tunbenjasiri K, Pongking T, Sitthirach C, Kongsintaweesuk S, Roytrakul S, Charoenlappanit S PLoS One. 2024; 19(5):e0301907.

PMID: 38814931 PMC: 11139331. DOI: 10.1371/journal.pone.0301907.


The interplay between monosodium glutamate (MSG) consumption and metabolic disorders.

Kayode O, Bello J, Oguntola J, Kayode A, Olukoya D Heliyon. 2023; 9(9):e19675.

PMID: 37809920 PMC: 10558944. DOI: 10.1016/j.heliyon.2023.e19675.


Beyond Plants: The Ultra-Processing of Global Diets Is Harming the Health of People, Places, and Planet.

Prescott S, DAdamo C, Holton K, Ortiz S, Overby N, Logan A Int J Environ Res Public Health. 2023; 20(15).

PMID: 37569002 PMC: 10419141. DOI: 10.3390/ijerph20156461.


Gut microbiota and neonatal acute kidney injury biomarkers.

Yang K, Du G, Liu J, Zhao S, Dong W Pediatr Nephrol. 2023; 38(11):3529-3547.

PMID: 36997773 DOI: 10.1007/s00467-023-05931-z.


References
1.
Gryp T, Vanholder R, Vaneechoutte M, Glorieux G . p-Cresyl Sulfate. Toxins (Basel). 2017; 9(2). PMC: 5331431. DOI: 10.3390/toxins9020052. View

2.
Luo Q, Cheng D, Huang C, Li Y, Lao C, Xia Y . Improvement of Colonic Immune Function with Soy Isoflavones in High-Fat Diet-Induced Obese Rats. Molecules. 2019; 24(6). PMC: 6470843. DOI: 10.3390/molecules24061139. View

3.
Edgar R . UPARSE: highly accurate OTU sequences from microbial amplicon reads. Nat Methods. 2013; 10(10):996-8. DOI: 10.1038/nmeth.2604. View

4.
Wang Q, Garrity G, Tiedje J, Cole J . Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl Environ Microbiol. 2007; 73(16):5261-7. PMC: 1950982. DOI: 10.1128/AEM.00062-07. View

5.
Hsu C, Lu P, Lo M, Lin I, Chang-Chien G, Lin S . Gut Microbiota-Dependent Trimethylamine -Oxide Pathway Associated with Cardiovascular Risk in Children with Early-Stage Chronic Kidney Disease. Int J Mol Sci. 2018; 19(12). PMC: 6320870. DOI: 10.3390/ijms19123699. View