E of normal homeostasis of the gut-liver axis. We hypothesized that acute alcohol consumption may affect gut microbiota and cause more bacterial products from the intestine to traffick to liver, which leads to the enhanced phagocytosis by hepatic macrophages and Kuffer cells. To test this hypothesis, we examined the composition of gut microbiota of alcohol treated IRAK-M deficient and sufficient mice. It is interesting that alcohol consumption caused a significant increase in culturable Gram-negative bacteria in both wild type and IRAKM deficient mice, but the increase of Gram-negative bacteria in the gut of IRAK-M deficient mice was greater. Alcohol consumption also caused a marked increase of gut permeability in IRAK-M deficient mice and this was not observed in wild type mice. Our results suggested that the gut-liver axis was indeed altered by acute alcohol consumption. In summary, our study provided Hesperidin web evidence that IRAK-M plays an important role in alcohol-induced liver injury and IRAK-M negatively regulates the innate and possibly adaptive immune response in the liver reacting to acute insult by alcohol. In the absence of IRAK-M, the hosts developed worse liver injury, altered inflammation, increased gut permeability and altered gutIRAK-M Regulates Liver Injurymicrobiota. We hope that the knowledge gained from this animal study will be useful for human studies.Author ContributionsContributed to supervision and the discussion of the study: HY IC. Conceived and designed the experiments: YW YM LW. Performed the experiments: YW YH CC MY. Analyzed the data: YW YH CC MY LW. Contributed reagents/materials/analysis tools: RAF. Wrote the paper: YW YM LW.AcknowledgmentsThe authors thank Xiaojun Zhang (Yale University) for her diligent care of the animals used in 18055761 this study, Changyun Hu (Yale University) for help with graphic work and F. Susan Wong (Cardiff University) for her critical reading of the manuscript.
Gastric cancer is one of the most frequently occurring cancers globally. A total of 989,600 new cases and 738,000 deaths are estimated to have occurred in 2008, accounting for 8 of the total number of cancer cases and 10 of cancer-related deaths [1]. The geographical distribution of gastric cancer exhibits wide international variation and .70 of new cases and deaths occur in developing countries. Investigations into the pathogenesis of gastric cancer have 
resulted in increasing evidence to suggest that interaction between various inherited cancer susceptibility genes could affect an individual’s risk of developing gastric cancer [2]. These genes are also known as risk-modifier genes, particularly those whose allelic polymorphisms are responsible for impaired metabolism of environmental carcinogens and/or repair of oxidative-stress-induced DNA damage. Since the first description by Krontiris in 1985 that the polymorphisms of the RAS gene can be used to assess the risk of oncogenesis [3], more studies have begun to demonstrateassociations between the polymorphisms and gastric cancer susceptibility, including oncogenes [4], antioncogenes [5,6] and immunomodifier genes [7,8]. It has also been suggested that genetic susceptibility genes, Lixisenatide especially genes for metabolic enzymes, may confer a risk for the development of gastric cancer [9?1]. Glutathione S-transferases (GSTS) consist of a superfamily of dimeric phase II metabolic enzymes [12]. Several polymorphisms in GST genes result in reduced or no activity of the enzymes. Specifically, GST.E of normal homeostasis of the gut-liver axis. We hypothesized that acute alcohol consumption may affect gut microbiota and cause more bacterial products from the intestine to traffick to liver, which leads to the enhanced phagocytosis by hepatic macrophages and Kuffer cells. To test this hypothesis, we examined the composition of gut microbiota of alcohol 
treated IRAK-M deficient and sufficient mice. It is interesting that alcohol consumption caused a significant increase in culturable Gram-negative bacteria in both wild type and IRAKM deficient mice, but the increase of Gram-negative bacteria in the gut of IRAK-M deficient mice was greater. Alcohol consumption also caused a marked increase of gut permeability in IRAK-M deficient mice and this was not observed in wild type mice. Our results suggested that the gut-liver axis was indeed altered by acute alcohol consumption. In summary, our study provided evidence that IRAK-M plays an important role in alcohol-induced liver injury and IRAK-M negatively regulates the innate and possibly adaptive immune response in the liver reacting to acute insult by alcohol. In the absence of IRAK-M, the hosts developed worse liver injury, altered inflammation, increased gut permeability and altered gutIRAK-M Regulates Liver Injurymicrobiota. We hope that the knowledge gained from this animal study will be useful for human studies.Author ContributionsContributed to supervision and the discussion of the study: HY IC. Conceived and designed the experiments: YW YM LW. Performed the experiments: YW YH CC MY. Analyzed the data: YW YH CC MY LW. Contributed reagents/materials/analysis tools: RAF. Wrote the paper: YW YM LW.AcknowledgmentsThe authors thank Xiaojun Zhang (Yale University) for her diligent care of the animals used in 18055761 this study, Changyun Hu (Yale University) for help with graphic work and F. Susan Wong (Cardiff University) for her critical reading of the manuscript.
Gastric cancer is one of the most frequently occurring cancers globally. A total of 989,600 new cases and 738,000 deaths are estimated to have occurred in 2008, accounting for 8 of the total number of cancer cases and 10 of cancer-related deaths [1]. The geographical distribution of gastric cancer exhibits wide international variation and .70 of new cases and deaths occur in developing countries. Investigations into the pathogenesis of gastric cancer have resulted in increasing evidence to suggest that interaction between various inherited cancer susceptibility genes could affect an individual’s risk of developing gastric cancer [2]. These genes are also known as risk-modifier genes, particularly those whose allelic polymorphisms are responsible for impaired metabolism of environmental carcinogens and/or repair of oxidative-stress-induced DNA damage. Since the first description by Krontiris in 1985 that the polymorphisms of the RAS gene can be used to assess the risk of oncogenesis [3], more studies have begun to demonstrateassociations between the polymorphisms and gastric cancer susceptibility, including oncogenes [4], antioncogenes [5,6] and immunomodifier genes [7,8]. It has also been suggested that genetic susceptibility genes, especially genes for metabolic enzymes, may confer a risk for the development of gastric cancer [9?1]. Glutathione S-transferases (GSTS) consist of a superfamily of dimeric phase II metabolic enzymes [12]. Several polymorphisms in GST genes result in reduced or no activity of the enzymes. Specifically, GST.
