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海马体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提取、保持和学习。

Sex differences in hippocampal β-adrenergic receptor subtypes drive retrieval, retention, and learning of cocaine-associated memories.

作者信息

Berry Melanie M, Miller Beau, Kelsen Silvia, Cockrell Carlee, Kohtz Amy Stave

机构信息

Department of Psychiatry, Division of Neurobiology and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.

Department of Biological Sciences, Mississippi College, Jackson, MS, United States.

出版信息

Front Behav Neurosci. 2024 May 14;18:1379866. doi: 10.3389/fnbeh.2024.1379866. eCollection 2024.

Abstract

BACKGROUND

Drug 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.

HYPOTHESIS

Prior 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.

METHODS

The 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).

RESULTS

In 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.

CONCLUSION

There 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.

摘要

背景

觅药行为是对环境背景和与药物相关线索的反应。这些普遍存在的刺激因素的存在阻碍了戒断的成功。β-肾上腺素能受体(β-ARs)长期以来一直被认为在驱动与情境记忆相关的过程中起作用,包括物质使用障碍中与药物相关的记忆。然而,β-肾上腺素能受体在药物记忆中的作用的性别差异仍然未知。

假设

先前的报告表明β2-ARs在雄性大鼠情境性药物记忆的提取和保持中具有选择性作用,并且雄性和雌性大鼠β-ARs的表达存在显著的性别差异。因此,我们假设在记忆编码和提取的不同阶段,β-ARs的选择性募集存在性别差异。

方法

使用可卡因条件性位置偏爱(CPP)实验,研究β-ARs在成年雄性和雌性Sprague-Dawley大鼠驱动可卡因情境记忆提取和学习中的作用。在测试(提取)前,或与每次可卡因(10mg/kg,腹腔注射)条件化训练(学习)配对时,将普萘洛尔(β1和β2)或ICI-118,551(β1)和/或倍他洛尔(β2)直接注入大鼠背侧海马。

结果

在雄性大鼠中,与注射溶剂相比,在首次CPP测试前给予β1、β2或联合给予β1和β2-ARs拮抗剂可降低CPP的表达。在雌性大鼠中,β2-ARs短暂降低CPP记忆,而β1具有持久但非即时的降低CPP记忆的作用。此外,β1以及联合给予β1和β2-ARs拮抗剂具有即时和持久的降低CPP记忆表达的作用。齿状回Fos+神经元预测雄性大鼠的可卡因CPP表达,而CA1和CA3区的Fos+神经元预测雌性大鼠的可卡因CPP表达。

结论

背侧海马β-ARs在可卡因条件性位置偏爱的编码和表达中的作用存在显著的性别差异。此外,在CPP过程中,雄性和雌性大鼠背侧海马的不同亚区似乎有不同的激活。因此,齿状回、CA3区和CA1区在驱动与药物相关或与情境相关线索方面可能具有独立的区域特异性和性别特异性影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e32a/11130369/a9b557e1524d/fnbeh-18-1379866-g001.jpg

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