啮齿动物早期生活压力后成瘾相关行为结果的性别差异

Millie Rincón-Cortés
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引用次数: 5

摘要

在人类中,早期生活压力(ELS)是后期生活中发生物质使用障碍(SUD)的一个既定风险因素。同样,暴露于ELS的啮齿类动物也表现出长期的酒精和药物消耗变化,这些ELS涉及母婴互动中断,如母亲分离(MS)或因有限的床上用品和筑巢(LBN)条件引起的稀缺逆境而产生的不良照顾。在人类和啮齿类动物中,都存在一系列与成瘾相关的行为,这些行为与药物使用有关,甚至可以预测随后的SUD。在啮齿类动物中,这些症状包括焦虑样行为、冲动和新奇感的增加,酒精和药物摄入模式的改变,以及涉及完善和社交行为的奖励相关过程的中断。重要的是,这些行为的表现在整个生命周期中往往是不同的。此外,临床前研究表明,性别差异在暴露于ELS如何影响奖赏和成瘾相关表型以及潜在的大脑奖赏回路中发挥作用。在这里,讨论了以MS和LBN形式的ELS导致的成瘾相关行为结果和中边缘多巴胺(DA)功能障碍,重点是年龄和性别依赖性影响。总的来说,这些发现表明,ELS可能通过干扰奖励相关大脑和行为功能的正常成熟,增加晚年药物使用和SUD的易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex differences in addiction-relevant behavioral outcomes in rodents following early life stress

In humans, exposure to early life stress (ELS) is an established risk factor for the development of substance use disorders (SUDs) during later life. Similarly, rodents exposed to ELS involving disrupted mother-infant interactions, such as maternal separation (MS) or adverse caregiving due to scarcity-adversity induced by limited bedding and nesting (LBN) conditions, also exhibit long-term alterations in alcohol and drug consumption. In both humans and rodents, there is a range of addiction-related behaviors that are associated with drug use and even predictive of subsequent SUDs. In rodents, these include increased anxiety-like behavior, impulsivity, and novelty-seeking, altered alcohol and drug intake patterns, as well as disrupted reward-related processes involving consummatory and social behaviors. Importantly, the expression of these behaviors often varies throughout the lifespan. Moreover, preclinical studies suggest that sex differences play a role in how exposure to ELS impacts reward and addiction-related phenotypes as well as underlying brain reward circuitry. Here, addiction-relevant behavioral outcomes and mesolimbic dopamine (DA) dysfunction resulting from ELS in the form of MS and LBN are discussed with a focus on age- and sex-dependent effects. Overall, these findings suggest that ELS may increase susceptibility for later life drug use and SUDs by interfering with the normal maturation of reward-related brain and behavioral function.

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来源期刊
Addiction neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
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