Literature DB >> 25469033

Gut microbiota in alcoholic liver disease: pathogenetic role and therapeutic perspectives.

Giulia Malaguarnera1, Maria Giordano1, Giuseppe Nunnari1, Gaetano Bertino1, Michele Malaguarnera1.   

Abstract

Alcoholic liver disease (ALD) is the commonest cause of cirrhosis in many Western countries and it has a high rate of morbidity and mortality. The pathogenesis is characterized by complex interactions between metabolic intermediates of alcohol. Bacterial intestinal flora is itself responsible for production of endogenous ethanol through the fermentation of carbohydrates. The intestinal metabolism of alcohol produces a high concentration of toxic acetaldehyde that modifies gut permeability and microbiota equilibrium. Furthermore it causes direct hepatocyte damage. In patients who consume alcohol over a long period, there is a modification of gut microbiota and, in particular, an increment of Gram negative bacteria. This causes endotoxemia and hyperactivation of the immune system. Endotoxin is a constituent of Gram negative bacteria cell walls. Two types of receptors, cluster of differentiation 14 and Toll-like receptors-4, present on Kupffer cells, recognize endotoxins. Several studies have demonstrated the importance of gut-liver axis and new treatments have been studied in recent years to reduce progression of ALD modifying gut microbiota. It has focused attention on antibiotics, prebiotics, probiotics and synbiotics.

Entities:  

Keywords:  Alcoholic liver disease; Bacterial translocation; Dysbiosis; Endotoxin; Gut microbiota; Prebiotics; Probiotics; Synbiotic

Mesh:

Substances:

Year:  2014        PMID: 25469033      PMCID: PMC4248208          DOI: 10.3748/wjg.v20.i44.16639

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  118 in total

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Journal:  Nat Rev Immunol       Date:  2002-03       Impact factor: 53.106

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7.  Nitric oxide and its metabolites mediate ethanol-induced microtubule disruption and intestinal barrier dysfunction.

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8.  Reduction of Escherichia coli O157 in finishing beef cattle by various doses of Lactobacillus acidophilus in direct-fed microbials.

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9.  TLR4 enhances TGF-beta signaling and hepatic fibrosis.

Authors:  Ekihiro Seki; Samuele De Minicis; Christoph H Osterreicher; Johannes Kluwe; Yosuke Osawa; David A Brenner; Robert F Schwabe
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  39 in total

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2.  Knockout of the Gsta4 Gene in Male Mice Leads to an Altered Pattern of Hepatic Protein Carbonylation and Enhanced Inflammation Following Chronic Consumption of an Ethanol Diet.

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Review 3.  The dormant blood microbiome in chronic, inflammatory diseases.

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Review 5.  Microbiota-based treatments in alcoholic liver disease.

Authors:  Hotaik Sung; Seung Woo Kim; Meegun Hong; Ki Tae Suk
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Review 6.  Hepatocellular carcinoma and the risk of occupational exposure.

Authors:  Venerando Rapisarda; Carla Loreto; Michele Malaguarnera; Annalisa Ardiri; Maria Proiti; Giuseppe Rigano; Evelise Frazzetto; Maria Irene Ruggeri; Giulia Malaguarnera; Nicoletta Bertino; Mariano Malaguarnera; Vito Emanuele Catania; Isidoro Di Carlo; Adriana Toro; Emanuele Bertino; Dario Mangano; Gaetano Bertino
Journal:  World J Hepatol       Date:  2016-05-08

Review 7.  Alcoholic liver disease: mechanisms of injury and targeted treatment.

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Review 8.  The role of the gut-brain axis in alcohol use disorders.

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9.  Alcohol use alters the colonic mucosa-associated gut microbiota in humans.

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10.  Kupffer Cell Metabolism and Function.

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