Castle Megan E, Flanigan Meghan E
Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, NC, 27599, USA.
Neurobiol Stress. 2024 Feb 20;30:100618. doi: 10.1016/j.ynstr.2024.100618. eCollection 2024 May.
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.
酒精使用障碍(AUD)是全球范围内导致死亡和残疾的主要原因之一,但目前的治疗方法在充分解决常常导致酒精消费复发的症状方面并不充分。几十年来,大脑的血清素系统一直与酒精使用障碍有关,并且是与酒精消费增加相关的应激相关行为的主要调节因子。本综述将讨论目前关于血清素系统的神经生物学适应性与人类酒精使用障碍之间关联的文献,以及血清素受体操纵对与酒精相关行为(如消费和戒断)的有效性。我们还将进一步讨论这些在人类中的发现与动物模型中的发现如何相关,包括对调节酒精消费的全身药理学操纵的比较。接下来,我们详细概述临床前动物模型中血清素和血清素受体信号在与酒精相关行为中的脑区特异性作用,强调在酒精使用障碍中形成血清素功能的连贯模型的复杂性,并提供更有效治疗干预的可能途径。在整个综述中,我们讨论了关于酒精使用障碍后遗症中的性别差异以及血清素在这些后遗症中的作用的已知情况。我们强调迫切需要对女性和雌性动物进行更多研究,以便我们能够建立一条更清晰的途径来阐明性别特异性血清素能机制并开发更好的治疗方法。