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首页> 外文期刊>Psychopharmacology >Further characterization of the prototypical nociceptin/orphanin FQ peptide receptor agonist Ro 64-6198 in rodent models of conflict anxiety and despair
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Further characterization of the prototypical nociceptin/orphanin FQ peptide receptor agonist Ro 64-6198 in rodent models of conflict anxiety and despair

机译:在冲突性焦虑和绝望的啮齿动物模型中原型伤害感受肽/孤啡肽FQ肽受体激动剂Ro 64-6198的进一步表征

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摘要

Rationale Ro 64-6198, the prototypical non-peptide nociceptin/ orphanin FQ peptide (NOP) receptor agonist, has potent anxiolytic-like effects in several preclinical models and species. However the effects of Ro 64-6198 on distinctive anxiety-provoking conditions related to unconditioned conflict behavior as well as its role in despair-like behavior remain to be addressed. Objective Here we examined the effects of Ro 64-6198 on unconditioned conflict anxiety using stimuli with different salience and on regulation of autonomic reactivity and compared these to the effects of benzodiazepine receptor agonists. We also addressed the potential effects of Ro 64-6198 on despair-like behavior. Materials and methods Ro 64-6198 (0.1 to 10mg/kg i.p.) and either diazepam or chlordiazepoxide were tested in the Vogel conflict punished drinking test (VCT) in Sprague Dawley rats, in the social approach-avoidance (SAA) test in Lewis rats, in the novelty-induced hypophagia (NIH) in C57BL/6Jmice, and in stress-induced hyperthermia in NMRImice, as well as in the forced swim test (FST) in Sprague Dawley rats and the tail suspension test (TST) in C57BL/6J mice. Results Ro 64-6198 (0.3 to 3 mg/kg) dose-dependently produced anxiolytic-like effects in the VCT, SAA, NIH, and SIH, similar to benzodiazepine receptor agonists. Ro 64-6198 did not alter immobility time in the FST and TST. Conclusions Ro 64-6198 produced marked anxiolytic-like effects in response to a variety of mild to strong anxiogenic stimuli, whereas it did not facilitate depression-related behaviors. This data extend previous literature suggesting that NOP receptors are a viable target for the treatment of anxiety disorders.
机译:基本原理Ro 64-6198,原型非肽伤害性感受器/孤儿蛋白FQ肽(NOP)受体激动剂,在一些临床前模型和物种中具有有效的抗焦虑作用。然而,Ro 64-6198对与无条件冲突行为有关的独特的引起焦虑的条件及其在绝望样行为中的作用的影响仍有待解决。目的在这里,我们研究了Ro 64-6198对使用不同显着性刺激的无条件冲突焦虑的影响以及对自主神经反应的调节作用,并将其与苯二氮卓受体激动剂的作用进行了比较。我们还解决了Ro 64-6198对类似绝望行为的潜在影响。材料和方法Ro 64-6198(0.1至10mg / kg ip)和地西epa或氯二氮卓在Sprague Dawley大鼠中进行Vogel冲突惩罚饮酒测试(VCT),在Lewis大鼠中进行避免社交接近(SAA)测试,C57BL / 6Jmice的新奇诱导的吞咽(NIH),NMRImice的应激诱导的体温过高以及Sprague Dawley大鼠的强迫游泳试验(FST)和C57BL / 6J小鼠。结果Ro 64-6198(0.3至3 mg / kg)剂量依赖性地在VCT,SAA,NIH和SIH中产生类似抗焦虑药的作用,类似于苯二氮卓受体激动剂。 Ro 64-6198并未改变FST和TST中的固定时间。结论Ro 64-6198对各种轻度至强烈的焦虑发生刺激产生了明显的抗焦虑作用,而它却不促进与抑郁相关的行为。该数据扩展了先前的文献,表明NOP受体是治疗焦虑症的可行靶标。

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