scholarly journals Inhibition of miR122a by Lactobacillus rhamnosus GG Culture Supernatant Increases Intestinal Occludin Expression and Protects Mice from Alcoholic Liver Disease

2015 ◽  
Vol 29 (S1) ◽  
Author(s):  
Liming Liu ◽  
Cuiqing Zhao ◽  
Craig McClain ◽  
Wenke Feng
2021 ◽  
Vol 160 (6) ◽  
pp. S-16
Author(s):  
Fengyuan Li ◽  
Zelin Gu ◽  
Mengwei Jiang ◽  
Lihua Zhang ◽  
Wenke Feng ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (2) ◽  
pp. e0117451 ◽  
Author(s):  
Meegun Hong ◽  
Seung Woo Kim ◽  
Sang Hak Han ◽  
Dong Joon Kim ◽  
Ki Tae Suk ◽  
...  

2017 ◽  
Vol 6 (3) ◽  
pp. 1
Author(s):  
Bernice D. Karlton-Senaye ◽  
Rishipal Bansode ◽  
Priscilla Randolph ◽  
Leonard L. Williams

Patulin, a mycotoxin, which is a major contaminant in apple juices, has contributed immensely to the occurrence of liver diseases. Consumption of apple juice could over long period of time become harmful to the health of individuals with pre-existing liver disease. Probiotics are known for their role in patulin removal from aqueous media. In this study, we investigated the effects of a probiotic microorganism on patulin toxicity in hepatocellular carcinoma (HepG2) cells and established the protective effect of Lactobacillus rhamnosus (LGG) as mediated by induction of BH3-interacting domain antagonist (BID) in response to patulin toxicity. After 24 hours of patulin exposure followed by 24 hours of treatment with Lactobacillus rhamnosus, cells proliferation decreased with increasing patulin exposure in samples without LGG pre-treatment, whereas with increasing concentration of patulin, cells were relatively rescued in LGG treated samples. It was further observed that pre-treatment of LGG with polysaccharide gums led to a decline in cell proliferation with increasing patulin exposure. Compare to the control, the expression of p53 upregulated moderator of apoptosis (PUMA) increased slightly by 7 % at 10µM patulin exposure in treatment and decreased by 30% in untreated cell. However, the expression of BID decreased by 26% in treatment compared to the control. We further established that the protective effect of Lactobacillus rhamnosus was mediated by the inhibition of BID. Our findings suggest that Lactobacillus rhamnosus GG could potentially function as a therapeutic agent to reverse the damaging effect of patulin on the liver of individuals with pre-existing liver disease.


PLoS ONE ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. e80169 ◽  
Author(s):  
Yvonne Ritze ◽  
Gyöngyi Bárdos ◽  
Anke Claus ◽  
Veronika Ehrmann ◽  
Ina Bergheim ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Ting Wang ◽  
Zhe Wang ◽  
Zhipeng Yang ◽  
Xin Cui ◽  
Liang Yan ◽  
...  

In this work, we discovered a new fermentation broth that can prevent and regulate alcoholic liver disease (ALD) and intestinal flora, which fermented the mixture of Pueraria lobata, Lonicera japonica, and Crataegus pinnatifida by Lactobacillus rhamnosus 217-1. The contents of polyphenols, puerarin, total isoflavones, and amino acids were significantly increased. Animal experiments showed that the fermentation broth could improve the liver indexes of ALD mice model, increase the activity of superoxide dismutase and glutathione in liver tissue, and reduce the level of malondialdehyde (MDA). Furthermore, the fermentation broth can reduce the levels of serum lipopolysaccharide (LPS), inflammatory factors interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α). Importantly, intestinal flora analysis showed that the fermentation broth could increase the abundance of Lactobacillales and reduce the production of Gram-negative bacteria, thereby reducing the abnormal increase in bacterial diversity caused by alcohol. In conclusion, we may have discovered a new functional food raw material with great application potential. The above findings indicate that the fermentation broth can actively regulate the intestinal flora and improve liver inflammation. The underlying mechanism might be that the fermentation broth could enhance intestinal permeability and reduce the inflammatory signals and LPS transmitted through the gut-liver axis, thereby reducing the oxidative stress and inflammation of the liver caused by alcohol.


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