scholarly journals The role of FoxO4 in the relationship between alcohol-induced intestinal barrier dysfunction and liver injury

2013 ◽  
Vol 31 (3) ◽  
pp. 569-576 ◽  
Author(s):  
BING CHANG ◽  
LIXUAN SANG ◽  
YING WANG ◽  
JING TONG ◽  
BINGYUAN WANG
Shock ◽  
2012 ◽  
Vol 38 (4) ◽  
pp. 436-443 ◽  
Author(s):  
Mingzhang Guo ◽  
Sarah Y. Yuan ◽  
Bert J. Frederich ◽  
Chongxiu Sun ◽  
Qiang Shen ◽  
...  

2020 ◽  
Vol 26 (20) ◽  
pp. 2426-2437 ◽  
Author(s):  
Alicia Rodriguez-Gonzalez ◽  
Laura Orio

In recent years, there has been an exciting focus of research attempting to understand neuropsychiatric disorders from a holistic perspective in order to determine the role of gut microbiota in the aetiology and pathogenesis of such disorders. Thus, the possible therapeutic benefits of targeting gut microbiota are being explored for conditions such as stress, depression or schizophrenia. Growing evidence indicates that there is bidirectional communication between gut microbiota and the brain that has an effect on normal CNS functioning and behavioural responses. Alcohol abuse damages the gastrointestinal tract, alters gut microbiota and induces neuroinflammation and cognitive decline. The relationship between alcohol abuse and hypothalamic-pituitary-adrenal axis activation, inflammation and immune regulation has been well documented. In this review, we explore the connection between microbiota, brain function and behaviour, as well as the mechanisms through which alcohol induces microbiota dysbiosis and intestinal barrier dysfunction. Finally, we propose the study of psychobiotics as a novel pharmaceutical strategy to treat alcohol use disorders.


2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Shengchun Dang ◽  
Yao Shen ◽  
Kai Yin ◽  
Jianxin Zhang

Severe acute pancreatitis (SAP) can cause intestinal barrier dysfunction (IBD), which significantly increases the disease severity and risk of mortality. We hypothesized that the innate immunity- and inflammatory-related protein-triggering receptor expressed on myeloid cells-1 (TREM-1) contributes to this complication of SAP. Thus, we investigated the effect of TREM-1 pathway modulation on a rat model of pancreatitis-associated IBD. In this study we sought to clarify the role of TREM-1 in the pathophysiology of intestinal barrier dysfunction in SAP. Specifically, we evaluated levels of serum TREM-1 and membrane-bound TREM-1 in the intestine and pancreas from an animal model of experimentally induced SAP. TREM-1 pathway blockade by LP17 treatment may suppress pancreatitis-associated IBD and ameliorate the damage to the intestinal mucosa barrier.


2019 ◽  
pp. e12574 ◽  
Author(s):  
Ting Gao ◽  
Zixu Wang ◽  
Yulan Dong ◽  
Jing Cao ◽  
Rutao Lin ◽  
...  

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