海马β肾上腺素能受体亚型的性别差异驱动可卡因相关记忆的检索、保持和学习

IF 2.6 3区 医学 Q2 BEHAVIORAL SCIENCES
Melanie M. Berry, Beau Miller, Silvia Kelsen, Carlee Cockrell, Amy Stave Kohtz
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引用次数: 0

摘要

背景寻求毒品的行为是对环境背景和毒品相关线索的反应。这些普遍存在的刺激会阻碍戒毒的成功。长期以来,β肾上腺素能受体(β-ARs)一直在驱动与情境记忆相关的过程,包括药物使用障碍中的药物相关记忆。假说先前的报告表明,β2-ARs 在雄性大鼠的情境记忆检索和保持中起着选择性作用,而雌雄大鼠的 β-ARs 表达也存在很大的性别差异。因此,我们假设在记忆编码和检索的不同阶段,β-ARs的选择性招募存在性别差异。方法利用可卡因条件性位置偏好(CPP)研究了成年雄性和雌性Sprague-Dawley大鼠β-ARs在可卡因情境记忆检索和学习中的作用。在测试(检索)之前,或在每次可卡因(10 mg/kp, IP)条件反射(学习)之前,直接向大鼠海马背侧输注普萘洛尔(β1 和 β2)或 ICI-118,551 (β1)和/或倍他洛尔(β2)。结果与车辆给药相比,男性在最初的CPP测试前服用β1、β2或联合服用β1和β2-ARs可减少CPP的表达。在雌性动物中,β2-ARs 可短暂减少 CPP 记忆,而 β1 具有长期持续的效果,但不能立即减少 CPP 记忆。此外,β1以及β1和β2-ARs的联合作用对减少CPP记忆的表达有直接和持续的影响。结论海马背侧β-ARs在可卡因条件性位置偏好的编码和表达中的作用存在显著的性别差异。此外,在可卡因条件性位置偏好过程中,雌雄大鼠海马背侧子区域的激活似乎也不同。因此,DG、CA3和CA1在驱动与药物相关或与情境相关的线索时可能具有不同区域和性别的特异性影响。
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 hippocampal β-adrenergic receptor subtypes drive retrieval, retention, and learning of cocaine-associated memories
BackgroundDrug seeking behavior occurs in response to environmental contexts and drug-associated cues. The presence of these pervasive stimuli impedes abstinence success. β-adrenergic receptors (β-ARs) have a long-standing historical implication in driving processes associated with contextual memories, including drug-associated memories in substance use disorders. However, sex differences in the role of β-adrenergic receptors in drug memories remain unknown.HypothesisPrior reports indicate a selective role for β2-ARs in retrieval and retention of contextual drug memories in males, and substantial sex differences exist in the expression of β-ARs of male and female rats. Therefore, we hypothesized that there are sex differences in selective recruitment of β-ARs during different stages of memory encoding and retrieval.MethodsThe role of β-ARs in driving retrieval and learning of contextual cocaine memories was investigated using cocaine conditioned place preference (CPP) in adult male and female Sprague–Dawley rats. Rats were infused directly to the dorsal hippocampus with Propranolol (β1 and β2) or ICI-118,551 (β1) and/or Betaxolol (β2), immediately prior to testing (retrieval), or paired to each cocaine (10 mg/kp, IP) conditioning session (learning).ResultsIn males, administration of either β1, β2, or combined β1 and β2-ARs before the initial CPP testing reduced the expression of a CPP compared to vehicle administration. In females, β2-ARs transiently decreased CPP memories, whereas β1 had long lasting but not immediate effects to decrease CPP memories. Additionally, β1 and combined β1 and β2-ARs had immediate and persistent effects to decrease CPP memory expression. DG Fos + neurons predicted cocaine CPP expression in males, whereas CA1 and CA3 Fos + neurons predicted cocaine CPP expression in females.ConclusionThere are significant sex differences in the role of dorsal hippocampus β-ARs in the encoding and expression of cocaine conditioned place preference. Furthermore, sub regions of the dorsal hippocampus appear to activate differently between male and female rats during CPP. Therefore DG, CA3, and CA1 may have separate region- and sex-specific impacts on driving drug- associated, or context-associated cues.
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来源期刊
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience BEHAVIORAL SCIENCES-NEUROSCIENCES
CiteScore
4.70
自引率
3.30%
发文量
506
审稿时长
6-12 weeks
期刊介绍: Frontiers in Behavioral Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the neural mechanisms underlying behavior. Field Chief Editor Nuno Sousa at the Instituto de Pesquisa em Ciências da Vida e da Saúde (ICVS) is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. This journal publishes major insights into the neural mechanisms of animal and human behavior, and welcomes articles studying the interplay between behavior and its neurobiological basis at all levels: from molecular biology and genetics, to morphological, biochemical, neurochemical, electrophysiological, neuroendocrine, pharmacological, and neuroimaging studies.
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