The role of brain serotonin signaling in excessive alcohol consumption and withdrawal: A call for more research in females

被引:5
作者
Castle, Megan E. [1 ]
Flanigan, Meghan E. [1 ]
机构
[1] Univ N Carolina, Bowles Ctr Alcohol Studies, Sch Med, Chapel Hill, NC 27599 USA
来源
NEUROBIOLOGY OF STRESS | 2024年 / 30卷
基金
美国国家卫生研究院;
关键词
Alcohol; Serotonin; Sex differences; DORSAL RAPHE NUCLEUS; CORTICOTROPIN-RELEASING-FACTOR; VENTRAL TEGMENTAL AREA; RECEPTOR MESSENGER-RNA; VOLUNTARY ETHANOL INTAKE; NATIONAL EPIDEMIOLOGIC SURVEY; 5-HT3 ANTAGONIST ONDANSETRON; SEX-DIFFERENCES; TRYPTOPHAN-HYDROXYLASE; TRANSPORTER GENE;
D O I
10.1016/j.ynstr.2024.100618
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alcohol Use Disorder (AUD) is a leading cause of death and disability worldwide, but current treatments are insufficient in fully addressing the symptoms that often lead to relapses in alcohol consumption. The brain's serotonin system has been implicated in AUD for decades and is a major regulator of stress-related behaviors associated with increased alcohol consumption. This review will discuss the current literature on the association between neurobiological adaptations in serotonin systems and AUD in humans as well as the effectiveness of serotonin receptor manipulations on alcohol-related behaviors like consumption and withdrawal. We will further discuss how these findings in humans relate to findings in animal models, including a comparison of systemic pharmacological manipulations modulating alcohol consumption. We next provide a detailed overview of brain region-specific roles for serotonin and serotonin receptor signaling in alcohol-related behaviors in preclinical animal models, highlighting the complexity of forming a cohesive model of serotonin function in AUD and providing possible avenues for more effective therapeutic intervention. Throughout the review, we discuss what is known about sex differences in the sequelae of AUD and the role of serotonin in these sequelae. We stress a critical need for additional studies in women and female animals so that we may build a clearer path to elucidating sex-specific serotonergic mechanisms and develop better treatments.
引用
收藏
页数:17
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