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神经降压素1型受体激动剂的抗精神病样作用

Antipsychotic-like effects of a neurotensin receptor type 1 agonist.

作者信息

Vadnie Chelsea A, Ayers-Ringler Jennifer, Oliveros Alfredo, Abulseoud Osama A, Choi Sun, Hitschfeld Mario J, Choi Doo-Sup

机构信息

Neurobiology of Disease Program, Mayo Graduate School, Rochester, MN, USA; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, MN, USA.

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, MN, USA.

出版信息

Behav Brain Res. 2016 May 15;305:8-17. doi: 10.1016/j.bbr.2016.02.019. Epub 2016 Feb 22.

DOI:10.1016/j.bbr.2016.02.019
PMID:26909848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4808331/
Abstract

Although neurotensin (NT) analogs are known to produce antipsychotic-like effects, the therapeutic possibility of a brain penetrant NTS1 agonist in treating psychiatric disorders has not been well studied. Here, we examined whether PD149163, a brain-penetrant NTS1-specific agonist, displays antipsychotic-like effects in C57BL/6J mice by investigating the effect of PD149163 on amphetamine-mediated hyperactivity and amphetamine-induced disruption of prepulse inhibition. In addition, we assessed the effect of PD149163 on glycogen synthase kinase-3 (GSK-3) activity, a downstream molecular target of antipsychotics and mood stabilizers, using phospho-specific antibodies. PD149163 (0.1 and 0.5mg/kg) inhibited amphetamine-induced hyperactivity in mice, indicating that NTS1 activation inhibits psychomotor agitation. PD149163 (0.5mg/kg) also increased prepulse inhibition, suggesting that NTS1 activation reduces prepulse inhibition deficits which often co-occur with psychosis in humans. Interestingly, PD149163 increased the inhibitory serine phosphorylation on both GSK-3α and GSK-3β in a dose- and time-dependent manner in the nucleus accumbens and medial prefrontal cortex of the mice. Moreover, PD149163 inhibited GSK-3 activity in the nucleus accumbens and medial prefrontal cortex in the presence of amphetamine. Thus, like most current antipsychotics and mood stabilizers, PD149163 inhibited GSK-3 activity in cortico-striatal circuitry. Together, our findings indicate that PD149163 may be a novel antipsychotic.

摘要

尽管已知神经降压素(NT)类似物会产生抗精神病样效应,但脑渗透性NTS1激动剂在治疗精神疾病方面的治疗可能性尚未得到充分研究。在此,我们通过研究PD149163对苯丙胺介导的多动和苯丙胺诱导的前脉冲抑制破坏的影响,来检验一种脑渗透性NTS1特异性激动剂PD149163在C57BL/6J小鼠中是否具有抗精神病样效应。此外,我们使用磷酸特异性抗体评估了PD149163对糖原合酶激酶-3(GSK-3)活性的影响,GSK-3是抗精神病药物和情绪稳定剂的下游分子靶点。PD149163(0.1和0.5mg/kg)抑制了苯丙胺诱导的小鼠多动,表明NTS1激活抑制了精神运动性激越。PD149163(0.5mg/kg)还增加了前脉冲抑制,表明NTS1激活减少了前脉冲抑制缺陷,而这种缺陷在人类中常与精神病同时出现。有趣的是,PD149163在小鼠伏隔核和内侧前额叶皮质中以剂量和时间依赖性方式增加了GSK-3α和GSK-3β上的抑制性丝氨酸磷酸化。此外,在存在苯丙胺的情况下,PD149163抑制了伏隔核和内侧前额叶皮质中的GSK-3活性。因此,与大多数目前的抗精神病药物和情绪稳定剂一样,PD149163在皮质-纹状体回路中抑制了GSK-3活性。总之,我们的研究结果表明PD149163可能是一种新型抗精神病药物。

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