4.5 Review

Inflammatory responses to alcohol in the CNS: nuclear receptors as potential therapeutics for alcohol-induced neuropathologies

Journal

JOURNAL OF LEUKOCYTE BIOLOGY
Volume 100, Issue 5, Pages 951-959

Publisher

OXFORD UNIV PRESS
DOI: 10.1189/jlb.3MR0416-171R

Keywords

fetal alcohol spectrum disorders; alcohol use disorders; neuroinflammation; peroxisome proliferator-activated receptor; microglia

Funding

  1. U.S. National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism [AA018834, AA023723]
  2. National Institute of General Medical Sciences Institutional Development Award [P30 GM110702]

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Fetal alcohol spectrum disorder (FASD), which results from ethanol exposure during pregnancy, and alcohol use disorder (AUD), which includes both binge and chronic alcohol abuse, are strikingly common and costly at personal and societal levels. These disorders are associated with significant pathology, including that observed in the CNS. It is now appreciated in both humans and animal models that ethanol can induce inflammation in the CNS. Neuroinflammation is hypothesized to contribute to the neuropathologic and behavioral consequences in FASD and AUD. In this review, we: 1) summarize the evidence of alcohol-induced CNS inflammation, 2) outline cellular and molecular mechanisms that may underlie alcohol induction of CNS inflammation, and 3) discuss the potential of nuclear receptor agonists for prevention or treatment of neuropathologies associated with FASD and AUD.

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