| Literature DB >> 25175862 |
Lucy G Chastain1, Dipak K Sarkar2.
Abstract
Exposure to alcohol, during development or adulthood, may result in damage to the nervous system, which underlies neurological and cognitive disruptions observed in patients with alcohol-related disorders, including fetal alcohol spectrum disorders (FASDs) and alcohol-use disorders (AUDs). Both clinical and preclinical evidence suggest microglia, the immune cells of the central nervous system, play a key role in modulating alcohol-induced neurotoxicity. Particularly, microglia are implicated in alcohol-induced neuroinflammation and in alcohol-induced increases in oxidative stress, which can lead to neuronal apoptosis. Recent studies also suggest a regenerative role for microglia in reestablishing homeostasis after alcohol exposure. These studies are summarized and reviewed in this chapter with emphasis on relevance to FASD and AUD.Entities:
Keywords: Alcohol; Alcohol-use disorder; Apoptosis; Fetal alcohol spectrum disorder; Inflammation; Microglia; Neurotoxicity; Reactive oxygen species
Mesh:
Substances:
Year: 2014 PMID: 25175862 DOI: 10.1016/B978-0-12-801284-0.00004-X
Source DB: PubMed Journal: Int Rev Neurobiol ISSN: 0074-7742 Impact factor: 3.230