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阿肯伯氏核壳内κ型阿片受体阻断可预防炎性痛对负面情绪状态的性别依赖性效应。

Sex-dependent effect of inflammatory pain on negative affective states is prevented by kappa opioid receptors blockade in the nucleus accumbens shell.

机构信息

Department of Pharmacy and Pharmaceutical Technology and Parasitology, University of Valencia, Valencia, Spain.

Department of Pharmacy and Pharmaceutical Technology and Parasitology, University of Valencia, Valencia, Spain; University Institute of Biotechnology and Biomedicine (BIOTECMED), University of Valencia, Valencia, Spain.

出版信息

Neuropharmacology. 2024 Jan 1;242:109764. doi: 10.1016/j.neuropharm.2023.109764. Epub 2023 Oct 23.

Abstract

Pain comorbidities include several psychological disorders, such as anxiety and anhedonia. However, the way pain affects male and female individuals and by which mechanism is not well understood. Previous research shows that pain induces alterations in the dynorphinergic pathway within the mesocorticolimbic system (MCLS), together with a relationship between corticotropin-releasing system and dynorphin release in the MCLS. Here, we analyse the sex and time course-dependent effects of pain on negative affect. Additionally, we study the implication of dynorphinergic and corticotropin releasing factor in these pain related behaviours. We used behavioural pharmacology and biochemical tools to characterise negative affective states induced by inflammatory pain in male and female rats, and the alterations in the dynorphinergic and the corticotropin systems within the MCLS. Female rats showed persistent anxiety-like and reversible anhedonia-like behaviours derived from inflammatory pain. Additionally, we found alterations in dynorphin and corticotropin releasing factor in NAc and amygdala, which suggests sex-dependent dynamic adaptations. Finally blockade on the kappa opioid receptor in the NAc confirmed its role in pain-induced anxiety-like behaviour in female rats. Our results show sex and time-dependent anxiety- and anhedonia-like behaviours induced by the presence of pain in female rats. Furthermore, we replicated previous data, pointing to the KOR/DYN recruitment in the NAc as a key neurological substrate mediating pain-induced behavioural alterations. This research studies the mechanisms underlying these behaviours, to better understand the emotional dimension of pain.

摘要

疼痛共病包括多种心理障碍,如焦虑和快感缺失。然而,疼痛如何影响男性和女性个体以及通过何种机制尚不清楚。先前的研究表明,疼痛会在中脑边缘皮质系统(MCLS)内引起强啡肽能途径的改变,同时 MCLS 中的促肾上腺皮质释放系统与强啡肽释放之间存在关系。在这里,我们分析了疼痛对负面情绪的性别和时间依赖性影响。此外,我们研究了强啡肽能和促肾上腺皮质释放因子在这些与疼痛相关的行为中的作用。我们使用行为药理学和生化工具来描述雄性和雌性大鼠炎症性疼痛引起的负面情绪状态,以及 MCLS 内强啡肽能和促肾上腺皮质释放系统的变化。雌性大鼠表现出持久的焦虑样和可逆的快感缺失样行为,源自炎症性疼痛。此外,我们发现 NAc 和杏仁核中的强啡肽和促肾上腺皮质释放因子发生改变,这表明存在性别依赖性的动态适应。最后,在 NAc 中阻断κ阿片受体证实了其在雌性大鼠疼痛引起的焦虑样行为中的作用。我们的研究结果显示,雌性大鼠存在疼痛时会出现性别和时间依赖性的焦虑和快感缺失样行为。此外,我们复制了先前的数据,表明 NAc 中的 KOR/DYN 募集是介导疼痛引起的行为改变的关键神经底物。这项研究探讨了这些行为的潜在机制,以更好地理解疼痛的情绪维度。

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