Suppr超能文献

阿立哌唑对 MK-801 诱导的前脉冲抑制缺陷和丝裂原活化蛋白激酶信号转导通路的影响。

Effects of aripiprazole on MK-801-induced prepulse inhibition deficits and mitogen-activated protein kinase signal transduction pathway.

机构信息

Department of Integrative Neurophysiology, Chiba University Graduate School of Medicine, 1-8-1 Inohana, Chiba 260-8670, Japan.

出版信息

Neurosci Lett. 2010 Feb 26;471(1):53-7. doi: 10.1016/j.neulet.2010.01.010. Epub 2010 Jan 18.

Abstract

Based on NMDA hypofunction hypothesis for negative symptoms and cognitive deficits in schizophrenia, MK-801-induced animal models of schizophrenia may help us understand the different effects between typical and atypical antipsychotics. On the other hand, the mitogen-activated protein kinase (MAPK) signaling pathways may participate in antipsychotic actions. The aim of this study was to investigate the effects of aripiprazole on MK-801-induced prepulse inhibition (PPI) disruption and MAPK phosphorylation in mice. To clarify the effects of aripiprazole on MK-801-induced PPI disruption, we measured PPI of 51 ddY male mice after aripiprazole was administered 15 min prior to the injection of MK-801, and measured activation of cytosol and nuclear MAPK phosphorylation by western blotting. Aripiprazole (4.0 mg/kg) significantly reversed the MK-801 (0.15 mg/kg)-induced PPI deficits. Pretreatment of aripiprazole (40 mg/kg) had a tendency to suppress MK-801 (1.0 mg/kg)-induced pMEK/MEK (Ser218/222) activation. In addition, aripiprazole treatment showed a significant decrease of pERK/ERK. Our data suggested that aripiprazole may reverse MK-801-induced PPI deficits through regulation of MAPK phosphorylation in the same way as the atypical antipsychotic drug, clozapine.

摘要

基于 NMDA 功能低下假说,即精神分裂症的阴性症状和认知缺陷,MK-801 诱导的精神分裂症动物模型可能有助于我们了解典型和非典型抗精神病药物的不同作用。另一方面,丝裂原活化蛋白激酶 (MAPK) 信号通路可能参与了抗精神病作用。本研究旨在探讨阿立哌唑对 MK-801 诱导的预脉冲抑制 (PPI) 破坏和 MAPK 磷酸化的影响。为了阐明阿立哌唑对 MK-801 诱导的 PPI 破坏的影响,我们在给予 MK-801 前 15 分钟给予阿立哌唑后,测量了 51 只 ddY 雄性小鼠的 PPI,并通过 Western blot 测量了细胞溶质和核 MAPK 磷酸化的激活。阿立哌唑 (4.0mg/kg) 显著逆转了 MK-801 (0.15mg/kg) 诱导的 PPI 缺陷。阿立哌唑 (40mg/kg) 的预处理有抑制 MK-801 (1.0mg/kg) 诱导的 pMEK/MEK (Ser218/222) 激活的趋势。此外,阿立哌唑治疗显示 pERK/ERK 显著减少。我们的数据表明,阿立哌唑可能通过调节 MAPK 磷酸化,与非典型抗精神病药物氯氮平一样,逆转 MK-801 诱导的 PPI 缺陷。

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