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终纹床核中的 CB1 和 CB2 受体不同地调节大鼠的焦虑样行为。

CB and CB receptors in the bed nucleus of the stria terminalis differently modulate anxiety-like behaviors in rats.

机构信息

Laboratory of Pharmacology, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, SP, Brazil; Joint UFSCar-UNESP Graduate Program in Physiological Sciences, São Carlos, SP, Brazil.

Department of Pharmacology, Paulista Medicine School, São Paulo Federal University, São Paulo, Brazil.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2021 Aug 30;110:110284. doi: 10.1016/j.pnpbp.2021.110284. Epub 2021 Feb 18.

Abstract

The endocannabinoid system is implicated in anxiety, but the brain sites involved are not completely understood. The bed nucleus of the stria terminalis (BNST) has been related to anxiety and responses to aversive threats. Besides, endocannabinoid neurotransmission acting via CB receptors was identified in the BNST. However, the presence of CB receptors and the role of BNST endocannabinoid system in anxiety-like behaviors have never been reported. Therefore, this study investigated the presence of CB and CB receptors in the BNST and their role in anxiety-like behaviors. For this, gene expression of the endocannabinoid receptors was evaluated in samples from anterior and posterior BNST. Besides, behaviors were evaluated in the elevated plus-maze (EPM) in unstressed rats (trait anxiety-like behavior) and after exposure to restraint stress (restraint-evoked anxiety-like behavior) in rats treated with either the CB receptor antagonist AM251 or the CB receptor antagonist JTE907 into the anterior BNST. The presence of CB and CB receptors gene expression was identified in anterior and posterior divisions of the BNST. Bilateral microinjection of AM251 into the anterior BNST dose-dependently increased EPM open arms exploration in unstressed animals and inhibited the anxiety-like behavior in the EPM evoked by restraint. Conversely, intra-BNST microinjection of JTE907 decreased EPM open arms exploration in a dose-dependent manner and inhibited restraint-evoked behavioral changes in the EPM. Taken together, these results indicate that CB and CB receptors present in the BNST are involved in control of anxiety-like behaviors, and control by the latter is affected by previous stress experience.

摘要

内源性大麻素系统与焦虑有关,但涉及的大脑部位尚不完全清楚。终纹床核(BNST)与焦虑和对厌恶威胁的反应有关。此外,内源性大麻素通过 CB 受体在 BNST 中的神经传递已被确定。然而,BNST 中的 CB 受体及其内源性大麻素系统在焦虑样行为中的存在从未被报道过。因此,本研究调查了 BNST 中 CB 和 CB 受体的存在及其在焦虑样行为中的作用。为此,评估了前BNST 和后BNST 样本中内源性大麻素受体的基因表达。此外,在未应激大鼠(特质焦虑样行为)的高架十字迷宫(EPM)中评估行为,以及在接受 CB 受体拮抗剂 AM251 或 CB 受体拮抗剂 JTE907 治疗的大鼠中评估暴露于束缚应激后的 EPM 行为(束缚诱发的焦虑样行为)。在前 BNST 和后 BNST 中鉴定出 CB 和 CB 受体基因表达的存在。双侧 AM251 在前 BNST 的微注射剂量依赖性地增加了未应激动物 EPM 开放臂的探索,并且抑制了束缚引起的 EPM 中的焦虑样行为。相反,BNST 内微注射 JTE907 以剂量依赖的方式减少了 EPM 开放臂的探索,并抑制了 EPM 中束缚引起的行为变化。综上所述,这些结果表明 BNST 中的 CB 和 CB 受体参与了对焦虑样行为的控制,而后者的控制受先前应激体验的影响。

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