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脑岛中介糖皮质激素在焦虑中的作用。

The insula mediates the effects of glucocorticoids in anxiety.

机构信息

Laboratorio de Neurobiologia, Instituto de Ciencias Biomédicas, Facultad de Medicina y Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile.

Laboratorio de Neurobiologia, Instituto de Ciencias Biomédicas, Facultad de Medicina y Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile.

出版信息

Neuropharmacology. 2023 Oct 1;237:109620. doi: 10.1016/j.neuropharm.2023.109620. Epub 2023 May 30.

Abstract

Increased activity in the insula has been consistently reported to be associated with anxiety and anxiety-related disorders. However, little is known on how the insula regulates anxiety. The present study aims at determining the role of the insula on the effects of glucocorticoids in anxiety. A combination of pharmacological manipulations, including blockade of adrenal GC synthesis by metyrapone and intra-insular microinjections of corticosterone, corticosterone-BSA, mineralocorticoid receptor (MR) antagonist spironolactone and glucocorticoid receptor (GR) antagonist mifepristone, were used to assess the short-term (5 min) effects of intra-insular corticosterone in two anxiety-like behaviors in male Sprague-Dawley rats. The elevated plus maze (EPM) and Novelty Suppressed Feeding (hyponeophagia) were utilized. We found that corticosterone in the insula is sufficient to prevent the anxiolytic effects corticosterone synthesis blockade in anxiety, and that intra-insular corticosterone has anxiolytic or anxiogenic effects depending on the amount of corticosterone microinjected and the arousal associated to the test, without affecting the HPA axis. Glucocorticoid anxiolytic effects in the insula are mediated by MRs, while its anxiogenic effects are dependent on a mifepristone-sensitive membrane-bound mechanism. Anxiety appears to be modulated at the insula through a competition between fast MR-dependent anxiolytic and membrane-associated anxiogenic signaling pathways that orchestrate the behavioral response to stress and determines the resulting level of anxiety.

摘要

岛叶活动增加与焦虑和焦虑相关障碍一直有密切关联。然而,岛叶如何调节焦虑仍然知之甚少。本研究旨在确定岛叶在糖皮质激素对焦虑影响中的作用。我们使用了药理学操作的组合,包括用美替拉酮阻断肾上腺 GC 的合成,以及向岛叶内微注射皮质酮、皮质酮-BSA、盐皮质激素受体(MR)拮抗剂螺内酯和糖皮质激素受体(GR)拮抗剂米非司酮,来评估皮质酮在雄性 Sprague-Dawley 大鼠的两种焦虑样行为中的短期(5 分钟)作用。使用高架十字迷宫(EPM)和新异抑制摄食(hyponeophagia)来评估。我们发现,岛叶内的皮质酮足以防止皮质酮合成阻断的抗焦虑作用,而且岛叶内皮质酮具有抗焦虑或致焦虑作用,这取决于皮质酮的微注射量和与测试相关的觉醒程度,而不影响 HPA 轴。糖皮质激素在岛叶中的抗焦虑作用是通过 MR 介导的,而其致焦虑作用则依赖于米非司酮敏感的膜结合机制。焦虑似乎是通过在岛叶内快速的 MR 依赖性抗焦虑和与膜相关的致焦虑信号通路之间的竞争来调节的,这些信号通路协调了对压力的行为反应,并决定了最终的焦虑水平。

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