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Functional Magnetic Resonance Imaging Reveals Different Neural Substrates for the Effects of Orexin-1 and Orexin-2 Receptor Antagonists

机译:功能磁共振成像揭示了不同的神经基质对Orexin-1和Orexin-2受体拮抗剂的影响

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摘要

Orexins are neuro-modulatory peptides involved in the control of diverse physiological functions through interaction with two receptors, orexin-1 (OX1R) and orexin-2 (OX2R). Recent evidence in pre-clinical models points toward a putative dichotomic role of the two receptors, with OX2R predominantly involved in the regulation of the sleep/wake cycle and arousal, and the OX1R being more specifically involved in reward processing and motivated behaviour. However, the specific neural substrates underlying these distinct processes in the rat brain remain to be elucidated. Here we used functional magnetic resonance imaging (fMRI) in the rat to map the modulatory effect of selective OXR blockade on the functional response produced by D-amphetamine, a psychostimulant and arousing drug that stimulates orexigenic activity. OXR blockade was produced by GSK1059865 and JNJ1037049, two novel OX1R and OX2R antagonists with unprecedented selectivity at the counter receptor type. Both drugs inhibited the functional response to D-amphetamine albeit with distinct neuroanatomical patterns: GSK1059865 focally modulated functional responses in striatal terminals, whereas JNJ1037049 induced a widespread pattern of attenuation characterised by a prominent cortical involvement. At the same doses tested in the fMRI study, JNJ1037049 exhibited robust hypnotic properties, while GSK1059865 failed to display significant sleep-promoting effects, but significantly reduced drug-seeking behaviour in cocaine-induced conditioned place preference. Collectively, these findings highlight an essential contribution of the OX2R in modulating cortical activity and arousal, an effect that is consistent with the robust hypnotic effect exhibited by JNJ1037049. The subcortical and striatal pattern observed with GSK1059865 represent a possible neurofunctional correlate for the modulatory role of OX1R in controlling reward-processing and goal-oriented behaviours in the rat.
机译:Orexins是一种神经调节肽,通过与两个受体orexin-1(OX1R)和orexin-2(OX2R)相互作用来参与多种生理功能的控制。临床前模型中的最新证据表明,这两种受体具有假定的二分作用,其中OX2R主要参与睡眠/唤醒周期和唤醒的调节,而OX1R更具体地参与奖励过程和动机行为。然而,尚待阐明在大鼠脑中这些不同过程背后的特定神经基质。在这里,我们在大鼠中使用功能磁共振成像(fMRI)来绘制选择性OXR阻滞对D-苯丙胺产生的功能反应的调节作用,D-苯丙胺是一种刺激刺激性和促发性活动的精神刺激药和刺激性药物。 OXR阻滞剂是由GSK1059865和JNJ1037049(两种新型的OX1R和OX2R拮抗剂)产生的,它们在反受体类型上具有空前的选择性。两种药物均抑制D-苯异丙胺的功能性反应,尽管具有明显的神经解剖学模式:GSK1059865会在纹状体末端局部调节功能性反应,而JNJ1037049则诱导了广泛的衰减模式,其特征是皮层受累。在功能磁共振成像研究中测试的相同剂量下,JNJ1037049表现出强大的催眠特性,而GSK1059865未能表现出显着的促睡眠作用,但在可卡因诱导的条件性场所偏爱中显着降低了药物寻找行为。总而言之,这些发现突出了OX2R在调节皮层活动和唤醒中的重要作用,这一作用与JNJ1037049表现出的强大的催眠作用一致。用GSK1059865观察到的皮层下和纹状体模式代表了OX1R在控制大鼠奖励过程和目标导向行为中的调节作用的可能的神经功能相关性。

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