ABSTRACT There is accumulating evidence that alcohol consumption and especially alcohol withdrawal increase brain levels of known innate immune signaling molecules and cause neuroinflammation. It has been shown that microbiota… Click to show full abstract
ABSTRACT There is accumulating evidence that alcohol consumption and especially alcohol withdrawal increase brain levels of known innate immune signaling molecules and cause neuroinflammation. It has been shown that microbiota play a pivotal role in this process and affect central neurochemistry and behavior. Disruption of or alterations in the intimate cross‐talk between microbiome and brain may be a significant factor in many psychiatric disorders. Alterations in the composition of the microbiome, so called dysbiosis, may result in detrimental distortion of microbe‐host homeostasis modulating the hypothalamic‐pituitary‐adrenal axis. A variety of pathologies are associated with changes in the community structure and function of the gut microbiota, suggesting a link between dysbiosis and disease etiology, including irritable bowel syndrome depression, anxiety disorders, schizophrenia, and alcoholism. Despite a paucity of clinical studies in alcohol‐dependent humans, emerging data suggests that alcohol induced alterations of the microbiome may explain reward‐seeking behaviors as well as anxiety, depression, and craving in withdrawal and increase the risk of developing psychiatric disorders. HIGHLIGHTSMicrobiota play an important role in central neurochemistry, contributing to the neurobiology of many psychiatric disordersAlcohol induced alterations of the microbiome may contribute essentially to reward‐seeking behaviors and cravingTargeting altered microbiome may provide new treatment options in addictive disorders as well as other psychiatric diseases
               
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