Blood brain barrier as an interface for alcohol induced neurotoxicity during development

Ethanol consumption during pregnancy or lactation permanently impairs the development of the central nervous system (CNS), resulting in the spectrum of fetal alcohol disorders (FASD). FASD is a general term that covers a set of deficits in the embryo caused by gestational alcohol exposure, with fetal alcohol syndrome (FAS) considered the most serious. The clinical features of FAS include facial abnormalities, short stature, low body weight, and evidence of structural and/or functional damage to the central nervous system (CNS). The prevalence of FAS carriers worldwide is about 15 for every 10,000 live births (about 119,000 children with APS born per year). Epidemiological data in the US show that the incidence of FAS exceeds other congenital syndromes such as Down syndrome and spina bifida. The deleterious effects of ethanol appear in different brain regions, varying according to the dose and period of neural development when the embryo was exposed, and include: 1) microcephaly; 2) abnormalities in cortical development, with a significant decrease in gyrification; 3) agenesis or hypoplasia of the corpus callosum; and 4) cognitive and behavioral deficits (such as impaired memory and learning, speech difficulties, and hyperactivity). Current evidence indicates that CNS blood vessels are particularly affected by teratogenic ethanol. The CNS vasculature is composed of specialized endothelial cells that establish intimate interactions with astrocytes, pericytes, and microglia, constituting the neurovascular unit of the blood-brain barrier (BBB). Together with the fact that BBB exert protective function, it can prevent the passage of substances and drugs to treat diseases that affect the CNS. Pathological changes in the BBB, such as drug abuse during pregnancy, congenital infections, or ageing processes can drastically alter the molecular structure and vascular stability, disrupting the BBB and aggravating certain neurodegenerative and neurological diseases. In this review, we address the effects of alcohol exposure on the formation of the BBB, specifically describing the cellular and molecular events induced by ethanol in the physiology of endothelial cells and glial cells, as well as their interaction during CNS development.

Automated summary

Ethanol consumption during pregnancy or lactation permanently impairs the development of the central nervous system, resulting in fetal alcohol spectrum disorders (FASD). FASD encompasses a range of deficits in the embryo caused by alcohol exposure during gestation, with fetal alcohol syndrome (FAS) being the most severe. FAS is characterized by facial abnormalities, stunted growth, low body weight, and structural and/or functional damage to the central nervous system. Ethanol has deleterious effects on different brain regions, leading to microcephaly, abnormal cortical development, corpus callosum agenesis or hypoplasia, and cognitive and behavioral deficits. Teratogenic ethanol particularly affects the CNS blood vessels, which constitute the neurovascular unit of the blood-brain barrier (BBB). BBB disruption can worsen neurodegenerative and neurological diseases.