Abstract

Alcohol exposure during pregnancy disrupts the development of the brain and produces long lasting behavioral and cognitive impairments collectively known as Fetal Alcohol Spectrum Disorders (FASDs). FASDs are characterized by alterations in learning, working memory, social behavior and executive function. A large body of literature using preclinical prenatal alcohol exposure models reports alcohol-induced changes in architecture and activity in specific brain regions affecting cognition. While multiple putative mechanisms of alcohol’s long-lasting effects on morphology and behavior have been investigated, an area that has received less attention is the effect of alcohol on cell adhesion molecules (CAMs). The embryo/fetal development represents a crucial period for Central Nervous System (CNS) development during which the cell-cell interaction plays an important role. CAMs play a critical role in neuronal migration and differentiation, synaptic organization and function which may be disrupted by alcohol. In this review, we summarize the physiological structure and role of CAMs involved in brain development, review the current literature on prenatal alcohol exposure effects on CAM function in different experimental models and pinpoint areas needed for future study to better understand how CAMs may mediate the morphological, sensory and behavioral outcomes in FASDs.

Highlights

  • Maternal alcohol consumption during pregnancy is well recognized as an important public health concern

  • It has been shown the involvement of Neural cell adhesion molecule (NCAM) in the trafficking of the neurotransmitter receptor dopamine 2 (Xiao et al, 2009). Taken together these findings demonstrated that different prenatal alcohol exposure models affect significantly the NCAMs in brain region-dependent manner, confirming the role of this class of cell adhesion molecules (CAMs) as like alcohol target during Central Nervous System (CNS) development

  • Considering the important role by this class of cell adhesion molecules plays during CNS development and in learning and memory processes, further investigation is needed in order to evaluate the possible involvement of integrins in the cognitive deficits observed in Fetal Alcohol Spectrum Disorders (FASDs)

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Summary

INTRODUCTION

Maternal alcohol consumption during pregnancy is well recognized as an important public health concern. 20 years ago, the term Fetal Alcohol Spectrum Disorders (FASDs) was introduced to recognize the broad range of effects induced by maternal alcohol exposure (Koren et al, 2003; Sokol et al, 2003; Chudley et al, 2005; Cook et al, 2016). FASDs are characterized by impairments in working memory, response inhibition, and behavioral flexibility (Streissguth et al, 1991; Mattson et al, 1999; Green et al, 2009; Marquardt et al, 2020)

Fetal Alcohol Spectrum Disorder Symptoms
Alcohol Consumption During Pregnancy
Neural Cell Adhesion Molecule and Prenatal Alcohol Exposure
Prenatal Alcohol Exposure Affects Cadherin Expression and Interactions
Integrins and Prenatal Alcohol Exposure Effects
Reduction of protein expression
AREAS OF FUTURE FOCUS
Effects of Prenatal Alcohol Exposure Variables
Interactions of Sex and Prenatal Alcohol Exposure on Cell Adhesion Molecules
Findings
CONCLUSION

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