Suppr超能文献

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.

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。

相似文献

1
Antipsychotic-like effects of a neurotensin receptor type 1 agonist.
Behav Brain Res. 2016 May 15;305:8-17. doi: 10.1016/j.bbr.2016.02.019. Epub 2016 Feb 22.
2
Activation of neurotensin receptor type 1 attenuates locomotor activity.
Neuropharmacology. 2014 Oct;85:482-92. doi: 10.1016/j.neuropharm.2014.05.046. Epub 2014 Jun 11.
5
The reversal of amphetamine-induced locomotor activation by a selective neurotensin-1 receptor agonist does not exhibit tolerance.
Psychopharmacology (Berl). 2008 Oct;200(2):197-203. doi: 10.1007/s00213-008-1197-5. Epub 2008 Jun 21.
6
The neurotensin-1 receptor agonist PD149163 inhibits conditioned avoidance responding without producing catalepsy in rats.
Eur Neuropsychopharmacol. 2011 Jul;21(7):526-31. doi: 10.1016/j.euroneuro.2010.12.004. Epub 2011 Jan 28.
7
The effects of systemic NT69L, a neurotensin agonist, on baseline and drug-disrupted prepulse inhibition.
Behav Brain Res. 2003 Jul 14;143(1):7-14. doi: 10.1016/s0166-4328(03)00037-8.
8
Neurotensin in the nucleus accumbens reverses dopamine supersensitivity evoked by antipsychotic treatment.
Neuropharmacology. 2017 Sep 1;123:10-21. doi: 10.1016/j.neuropharm.2017.05.015. Epub 2017 May 15.

引用本文的文献

5
Neurotensin in reward processes.
Neuropharmacology. 2020 May 1;167:108005. doi: 10.1016/j.neuropharm.2020.108005. Epub 2020 Feb 11.
6
Chronic caffeine exposure in adolescence promotes diurnal, biphasic mood-cycling and enhanced motivation for reward in adult mice.
Behav Brain Res. 2019 Sep 16;370:111943. doi: 10.1016/j.bbr.2019.111943. Epub 2019 May 13.
7
Adenosine A receptor and ERK-driven impulsivity potentiates hippocampal neuroblast proliferation.
Transl Psychiatry. 2017 Apr 18;7(4):e1095. doi: 10.1038/tp.2017.64.
8
Sensorimotor gating of the startle reflex: what we said 25 years ago, what has happened since then, and what comes next.
J Psychopharmacol. 2016 Nov;30(11):1072-1081. doi: 10.1177/0269881116661075. Epub 2016 Aug 18.

本文引用的文献

4
Elucidating the role of neurotensin in the pathophysiology and management of major mental disorders.
Behav Sci (Basel). 2014 Jun 13;4(2):125-153. doi: 10.3390/bs4020125. eCollection 2014 Jun.
5
Activation of neurotensin receptor type 1 attenuates locomotor activity.
Neuropharmacology. 2014 Oct;85:482-92. doi: 10.1016/j.neuropharm.2014.05.046. Epub 2014 Jun 11.
6
Glycogen synthase kinase-3 inhibitors: Rescuers of cognitive impairments.
Pharmacol Ther. 2014 Jan;141(1):1-12. doi: 10.1016/j.pharmthera.2013.07.010. Epub 2013 Jul 31.
7
Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis.
Lancet. 2013 Sep 14;382(9896):951-62. doi: 10.1016/S0140-6736(13)60733-3. Epub 2013 Jun 27.
8
Hyperactivity: glycogen synthase kinase-3 as a therapeutic target.
Eur J Pharmacol. 2013 May 15;708(1-3):56-9. doi: 10.1016/j.ejphar.2013.02.055. Epub 2013 Mar 14.
10
Deletion of GSK3β in D2R-expressing neurons reveals distinct roles for β-arrestin signaling in antipsychotic and lithium action.
Proc Natl Acad Sci U S A. 2012 Dec 11;109(50):20732-7. doi: 10.1073/pnas.1215489109. Epub 2012 Nov 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验