Role of NMDAR Regulation in Phencyclidine-Induced Neurotoxicity

NMDAR 调节在苯环己哌啶诱导的神经毒性中的作用

• 批准号: 7496507
• 负责人: Noelle C Anastasio
• 金额: $ 1.94万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-09-27 至 2009-04-03
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7496507
• 关键词: Acute; Animals; Behavior; Binding; Brain region; Calpain; Cell Death; Chronic; Cities; Cleaved cell; Clinical; Corpus striatum structure; Cycloheximide; Development; Dissociative Anesthetics; Dopamine; Emotions; Endoplasmic Reticulum; Family; Glutamates; Glycine; Hallucinations; Human; Immunohistochemistry; Intoxication; Label; MDL 100907; Measures; Mediating; Membrane; Memory; N-Methyl-D-Aspartate Receptors; N-Methylaspartate; NR1 gene; Pathway Analysis; Perinatal; Phencyclidine; Postoperative Period; Process; Property; Protein Biosynthesis; Protein Synthesis Inhibitors; Proteins; Psychotic Disorders; Purpose; Rattus; Receptor Up-Regulation; Regulation; Reporting; Role; Schizophrenia; Serotonin; Serotonin Receptor 5-HT2A; Sulpiride; Symptoms; Thinking; Time; Tissue membrane; Transcriptional Activation; United States; Up-Regulation; Western Blotting; calpain inhibitor; caspase-3; density; dosage; drug of abuse; falls; frontal lobe; human NR1 protein; inhibitor/antagonist; insight; member; neurotoxic; neurotoxicity; protein expression; pup; receptor; receptor function; research study; serotonin receptor; trafficking

DESCRIPTION (provided by applicant): Clinical use of phencyclidine (PCP), a potent dissociative anesthetic, was abandoned because of reports of post-operative hallucinations and disoriented behavior. Due to its hallucinogenic effects, PCP appeared on the drug of abuse scene in the mid-1960's known as "angel dust" but its illicit use has substantially diminished because of its psychotomimetic properties. PCP intoxication in humans has also been shown to mimic both the positive and negative symptoms of schizophrenia as well as exacerbate psychoses in schizophrenics. PCP elicits its major actions as a noncompetitive NMDAR antagonist, a member of the ionotropic glutamate family of receptors. PCP administration in immature rats has been shown to cause.. neurotoxicity and later in development, aberrant behaviors. Preliminary experiments have shown that two distinct mechanisms of receptor trafficking and protein synthesis are likely involved in the differences in NMDAR up-regulation that exist between perinatal acute and sub-chronic PCP administration and that this may underlie regional- and dosage-dependent differences in the mechanism of PCP-induced neurotoxicity. The purpose of this study is to determine the mechanism and functional consequences of PCP-induced regulation of the NMDAR in association with neurotoxicity in the frontal cortex and striatum in perinatal rats. The specific aims of this project will focus on delineating the mechanisms of regulation of the NMDAR, specifically the role of synthesis and trafficking of the receptor following acute and sub-chronic PCP administration through the use of selective inhibitors of synthesis and trafficking pathways and analysis via Western blot. In addition, we plan to investigate the role of indirect activation of DA and 5-HT receptors on the NMDAR using 3H-MK-801 binding. Finally, in order to relate regulation and function of the NMDAR to NMDA-mediated cell death, we plan to incorporate double-labeled immunohistochemistry of the NR1 and NR2A/B subunits and a known marker of neurotoxicity, cleaved caspase-3. Lay Summary: PCP, also known as "angel dust", is a powerful psychoactive substance that is mainly abused in urban regions of several large cities in the United States. It elicits its actions through blockade of the NMDA receptor in brain regions responsible for memory, emotions, and higher thought processes. This project aims to further clarify the actions of PCP at the NMDA receptor in order to gain insight into the mechanisms underlying its hallucinogenic, psychotomimetic, and neurotoxic properties.

描述（由申请人提供）：临床使用苯环利定（PCP），一种强效解离性麻醉剂，由于术后出现幻觉和定向障碍行为的报告而被放弃。由于其致幻作用，PCP在20世纪60年代中期出现在毒品滥用现场，被称为“天使之尘”，但由于其模拟精神的特性，其非法使用已大大减少。人类PCP中毒也被证明模仿精神分裂症的阳性和阴性症状，并加剧精神分裂症患者的精神病。PCP的主要作用是非竞争性NMDAR拮抗剂，是嗜离子性谷氨酸受体家族的一员。未成熟大鼠服用PCP已被证明会导致…神经毒性和发育后期的异常行为。初步实验表明，两种不同的受体运输和蛋白质合成机制可能涉及围产期急性和亚慢性PCP给药之间存在的NMDAR上调差异，这可能是PCP诱导神经毒性机制区域和剂量依赖性差异的基础。本研究的目的是确定pcp诱导的NMDAR调控与围产儿大鼠额叶皮质和纹状体神经毒性相关的机制和功能后果。该项目的具体目标将集中在描述NMDAR的调节机制，特别是在急性和亚慢性PCP给药后，通过使用合成和运输途径的选择性抑制剂和Western blot分析，合成和运输受体的作用。此外，我们计划利用3H-MK-801结合来研究间接激活DA和5-HT受体在NMDAR中的作用。最后，为了将NMDAR的调控和功能与nmda介导的细胞死亡联系起来，我们计划结合NR1和NR2A/B亚基的双标记免疫组织化学和已知的神经毒性标记物cleaved caspase-3。概要：PCP，也被称为“天使之尘”，是一种强大的精神活性物质，主要在美国几个大城市的市区滥用。它通过阻断大脑中负责记忆、情绪和高级思维过程的区域的NMDA受体来引发其行为。本项目旨在进一步阐明PCP对NMDA受体的作用，以深入了解其致幻、拟精神和神经毒性的机制。