Journal
CURRENT OPINION IN NEUROBIOLOGY
Volume 23, Issue 4, Pages 513-520Publisher
CURRENT BIOLOGY LTD
DOI: 10.1016/j.conb.2013.01.024
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Funding
- NIAAA NIH HHS [R01 AA012404, U01 AA013520, P01 AA020683] Funding Source: Medline
- NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM [R01AA012404, U01AA013520, P01AA020683] Funding Source: NIH RePORTER
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Molecular and behavioral studies corroborate a pivotal role for the innate immune system in mediating the acute and chronic effects of alcohol and support a neuroimmune hypothesis of alcohol addiction. Changes in expression of neuroimmune genes and microglial transcripts occur in postmortem brain from alcoholics and animals exposed to alcohol, and null mutant animals lacking certain innate immune genes show decreased alcohol-mediated responses. Many of the differentially expressed genes are part of the toll like receptor (TLR) signaling pathway and culminate in an increased expression of pro-inflammatory immune genes. Compounds known to inhibit inflammation, microglial activation, and neuroimmune gene expression have shown promising results in reducing alcohol-mediated behaviors in animal models, indicating that neuroimmune signaling pathways offer unexplored targets in the treatment of alcohol abuse.
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