首页> 外文期刊>Behavioural Brain Research: An International Journal >Participation of dorsal periaqueductal gray 5-HT1A receptors in the panicolytic-like effect of the kappa-opioid receptor antagonist Nor-BNI
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Participation of dorsal periaqueductal gray 5-HT1A receptors in the panicolytic-like effect of the kappa-opioid receptor antagonist Nor-BNI

机译:背部PeriaqueDuctal灰色5-HT1A受体参与Kappa-Apioid受体拮抗剂Nor-BNI的泛冰效果

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Panic patients may have abnormalities in serotonergic and opioidergic neurotransmission. The dorsal periaqueductal gray (dPAG) plays an important role in organizing proximal defense, related to panic attacks. The 5-HT1A receptor (5-HT1A-R) is involved in regulating escape behavior that is organized in the dPAG. Activation of K-opioid receptor (KOR) in this region causes anxiogenic effects. In this study, we investigated the involvement of KOR in regulating escape behavior, using systemic and intra-dPAG injection of the KOR antagonist Nor-BNI. As panic models, we used the elevated T-maze (ETM) and the dPAG electrical stimulation test (EST). We also evaluated whether activation of the 5-HT1A-R or the opioid receptor (MOR) in the dPAG contributes to the Nor-BNI effects. The results showed that systemic administration of Nor-BNI, either subcutaneously (2.0 and 4.0 mg/kg) or intraperitoneally (2.0 mg/kg), impaired escape in the EST, indicating a panicolytic-like effect. Intra-dPAG injection of this antagonist (6.8 nmol) caused the same effect in the EST and in the ETM. Association of ineffective doses of Nor-BNI and the 5-HT1A-R agonist 8-OH-DPAT caused panicolytic-like effect in these two tests. Previous administration of the 5-HT1A-R antagonist WAY-100635, but not of the MOR antagonist CTOP, blocked the panicolytic-like effect of Nor-BNI. These results indicate that KOR enhances proximal defense in the dPAG through 5-HT1A-R modulation, independently of MOR. Because former results indicate that the 5HT(1A)-R is involved in the antipanic action of antidepressants, KOR antagonists may be useful as adjunctive or alternative drug treatment of panic disorder. (C) 2017 Elsevier B.V. All rights reserved.
机译:恐慌患者可能在Serotonergic和OpioidicGic神经递质中具有异常。背部PeriaqueDuctal灰色(DPAG)在组织近端防御方面发挥着重要作用,与恐慌发作有关。 5-HT1A受体(5-HT1A-R)参与调节在DPAG中组织的逃生行为。在该地区的K-阿片受体(Kor)的激活导致焦虑作用。在这项研究中,我们研究了Kor在调节逃生行为中的参与,利用KOR拮抗剂NOR-BNI的全身和DPAG注射。作为恐慌模型,我们使用了高迷宫(ETM)和DPAG电刺激测试(EST)。我们还评估了DPAG中5-HT1A-R或阿片受体(Mor)的活化是否有助于NOR-BNI效应。结果表明,无论是皮下(2.0和4.0mg / kg)或腹膜内(2.0mg / kg)的全身施用,在EST中逸出,表明良好的效果。 DPAG内部拮抗剂(6.8诺米尔)注射了对EST和ETM的效果相同。无效剂量的NOR-BNI和5-HT1A-R激动剂8-OH-DPAT的缔合在这两个测试中引起了良性的效果。以前的5-HT1A-R拮抗剂Way-100635施用,但不是Mor拮抗剂CTOP,阻断了NOR-BNI的泛冰状效果。这些结果表明,KOR通过5-HT1A-R调节,独立于MOR增强DPAG中的近端防御。因为前结果表明,5HT(1A)-R参与抗抑郁药的抗奥氏症作用,KOR拮抗剂可用作恐慌症的辅助或替代药物治疗。 (c)2017 Elsevier B.v.保留所有权利。

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