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伏隔核壳中的κ-阿片受体拮抗作用将酒精依赖中逐渐增加的酒精摄入量和负性情感样行为与生理戒断区分开来。

Kappa-opioid receptor antagonism in the nucleus accumbens shell distinguishes escalated alcohol consumption and negative affective-like behavior from physiological withdrawal in alcohol-dependence.

作者信息

Lepreux Gaetan, Henricks Angela M, Wei Gengze, Go Bok Soon, Erikson Chloe M, Abella Rachel M, Pham Amy, Walker Brendan M

机构信息

Department of Psychiatry and Behavioral Neurosciences, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.

Department of Psychology, Washington State University, Pullman, WA, USA.

出版信息

Pharmacol Biochem Behav. 2024 Oct;243:173840. doi: 10.1016/j.pbb.2024.173840. Epub 2024 Aug 7.

Abstract

Alcohol use disorder (AUD) is a chronic relapsing disease that is deleterious at individual, familial, and societal levels. Although AUD is one of the highest preventable causes of death in the USA, therapies for the treatment of AUD are not sufficient given the heterogeneity of the disorder and the limited number of approved medications. To provide better pharmacological strategies, it is important to understand the neurological underpinnings of AUD. Evidence implicates the endogenous dynorphin (DYN)/κ-opioid receptor (KOR) system recruitment in dysphoric and negative emotional states in AUD to promote maladaptive behavioral regulation. The nucleus accumbens shell (AcbSh), mediating motivational and emotional processes that is a component of the mesolimbic dopamine system and the extended amygdala, is an important site related to alcohol's reinforcing actions (both positive and negative) and neuroadaptations in the AcbSh DYN/KOR system have been documented to induce maladaptive symptoms in AUD. We have previously shown that in other nodes of the extended amygdala, site-specific KOR antagonism can distinguish different symptoms of alcohol dependence and withdrawal. In the current study, we examined the role of the KOR signaling in the AcbSh of male Wistar rats in operant alcohol self-administration, measures of negative affective-like behavior, and physiological symptoms during acute alcohol withdrawal in alcohol-dependence. To induce alcohol dependence, rats were exposed to chronic intermittent ethanol vapor for 14 h/day for three months, during which stable escalation of alcohol self-administration was achieved and pharmacological AcbSh KOR antagonism ensued. The results showed that AcbSh KOR antagonism significantly reduced escalated alcohol intake and negative affective-like states but did not alter somatic symptoms of withdrawal. Understanding the relative contribution of these different drivers is important to understand and inform therapeutic efficacy approaches in alcohol dependence and further emphasis the importance of the KOR/DYN system as a target for AUD therapeutics.

摘要

酒精使用障碍(AUD)是一种慢性复发性疾病,在个体、家庭和社会层面均具有危害性。尽管AUD是美国最可预防的死亡原因之一,但鉴于该疾病的异质性以及获批药物数量有限,用于治疗AUD的疗法并不充分。为了提供更好的药理学策略,了解AUD的神经学基础至关重要。有证据表明,内源性强啡肽(DYN)/κ-阿片受体(KOR)系统在AUD的烦躁不安和负性情绪状态中被激活,以促进适应不良的行为调节。伏隔核壳(AcbSh)介导动机和情感过程,是中脑边缘多巴胺系统和扩展杏仁核的组成部分,是与酒精强化作用(包括正向和负向)相关的重要部位,并且已证明AcbSh DYN/KOR系统中的神经适应性变化会在AUD中诱发适应不良症状。我们之前已经表明,在扩展杏仁核的其他节点中,位点特异性KOR拮抗作用可以区分酒精依赖和戒断的不同症状。在本研究中,我们研究了KOR信号在雄性Wistar大鼠AcbSh中对操作性酒精自我给药、负性情感样行为测量以及酒精依赖急性戒断期间生理症状的作用。为了诱导酒精依赖,大鼠每天暴露于慢性间歇性乙醇蒸气中14小时,持续三个月,在此期间实现了酒精自我给药的稳定增加,并随后进行了药理学上的AcbSh KOR拮抗。结果表明,AcbSh KOR拮抗作用显著降低了增加的酒精摄入量和负性情感样状态,但并未改变戒断的躯体症状。了解这些不同驱动因素的相对作用对于理解和指导酒精依赖的治疗效果方法很重要,并进一步强调了KOR/DYN系统作为AUD治疗靶点的重要性。

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