核团外壳中的卡巴-阿片受体拮抗作用可将酒精依赖症患者的酒精消费升级和负性情感样行为与生理戒断区分开来。

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
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引用次数: 0

摘要

酒精使用障碍(AUD)是一种慢性复发性疾病,对个人、家庭和社会都有危害。虽然 AUD 是美国最高的可预防死因之一,但鉴于该疾病的异质性和获批药物的有限性,治疗 AUD 的疗法并不充分。为了提供更好的药物治疗策略,了解 AUD 的神经学基础非常重要。有证据表明,内源性达诺啡肽(DYN)/κ-阿片受体(KOR)系统的招募与 AUD 中的焦虑和消极情绪状态有关,可促进不良行为调节。作为间叶多巴胺系统和扩展杏仁核的一个组成部分,阿隆伯斯核(AcbSh)介导动机和情绪过程,是与酒精的强化作用(包括积极和消极作用)相关的一个重要部位,有记录表明,阿隆伯斯核 DYN/KOR 系统的神经适应会诱发 AUD 的适应不良症状。我们之前已经证明,在扩展杏仁核的其他结节中,特定部位的 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,我们考察了雄性 Wistar 大鼠 AcbSh 中的 KOR 信号在酒精依赖急性戒断期的操作性酒精自我给药、负性情感样行为测量和生理症状中的作用。为了诱导酒精依赖症,大鼠被暴露于慢性间歇性乙醇蒸汽中,每天14小时,持续3个月,在此期间实现了稳定的酒精自我给药升级,随后进行药物AcbSh KOR拮抗。结果表明,AcbSh KOR拮抗剂能显著减少酒精摄入的升级和负面情绪样状态,但不会改变戒断的躯体症状。了解这些不同驱动因素的相对贡献对于理解和了解酒精依赖症的疗效方法非常重要,并进一步强调了 KOR/DYN 系统作为 AUD 治疗靶点的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kappa-opioid receptor antagonism in the nucleus accumbens shell distinguishes escalated alcohol consumption and negative affective-like behavior from physiological withdrawal in alcohol-dependence

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.

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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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