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Loss of object recognition memory produced by extended access to methamphetamine self-administration is reversed by positive allosteric modulation of metabotropic glutamate receptor 5.长期接触 methamphetamine 自身给药会导致物体识别记忆丧失,而代谢型谷氨酸受体 5 的正变构调节可逆转这种记忆丧失。
Neuropsychopharmacology. 2011 Mar;36(4):782-92. doi: 10.1038/npp.2010.212. Epub 2010 Dec 8.
2
Extended access to methamphetamine self-administration affects sensorimotor gating in rats.延长冰毒自我给药会影响大鼠的感觉运动门控。
Behav Brain Res. 2011 Mar 1;217(2):386-90. doi: 10.1016/j.bbr.2010.11.009. Epub 2010 Nov 9.
3
PROKR2 is associated with methamphetamine dependence in the Japanese population.PROKR2 与日本人群中的甲基苯丙胺依赖有关。
Prog Neuropsychopharmacol Biol Psychiatry. 2010 Aug 16;34(6):1033-6. doi: 10.1016/j.pnpbp.2010.05.018. Epub 2010 May 24.
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Aripiprazole attenuates established behavioral sensitization induced by methamphetamine.阿立哌唑可减弱甲基苯丙胺诱导的行为敏化。
Prog Neuropsychopharmacol Biol Psychiatry. 2010 Aug 16;34(6):1115-9. doi: 10.1016/j.pnpbp.2010.06.006. Epub 2010 Jun 16.
5
High dose D-serine in the treatment of schizophrenia.高剂量 D-丝氨酸治疗精神分裂症。
Schizophr Res. 2010 Aug;121(1-3):125-30. doi: 10.1016/j.schres.2010.05.012. Epub 2010 Jun 11.
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Adaptive immune regulation of glial homeostasis as an immunization strategy for neurodegenerative diseases.作为神经退行性疾病免疫策略的胶质细胞内稳态的适应性免疫调控。
J Neurochem. 2010 Sep 1;114(5):1261-76. doi: 10.1111/j.1471-4159.2010.06834.x. Epub 2010 May 26.
7
Association analysis of GRM2 and HTR2A with methamphetamine-induced psychosis and schizophrenia in the Japanese population.GRM2 和 HTR2A 与日本人群中甲基苯丙胺所致精神病和精神分裂症的关联分析。
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Methamphetamine and paranoia: the methamphetamine experience questionnaire.甲基苯丙胺和妄想:甲基苯丙胺体验问卷。
Am J Addict. 2010 Mar-Apr;19(2):155-68. doi: 10.1111/j.1521-0391.2009.00014.x.
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Control of neuroinflammation as a therapeutic strategy for amyotrophic lateral sclerosis and other neurodegenerative disorders.神经炎症的控制作为肌萎缩侧索硬化症和其他神经退行性疾病的治疗策略。
Exp Neurol. 2010 Mar;222(1):1-5. doi: 10.1016/j.expneurol.2009.12.018. Epub 2010 Jan 4.
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Methamphetamine use, dependence and treatment access in rural and regional North Coast of New South Wales, Australia.澳大利亚新南威尔士州北海岸农村和地区的甲基苯丙胺使用、依赖和治疗机会。
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甲基苯丙胺相关性精神病。

Methamphetamine-associated psychosis.

机构信息

Department of Internal Medicine, VA Nebraska-Western Iowa Health Care System, University of Nebraska Medical Center, Omaha, NE 68198-5300, USA.

出版信息

J Neuroimmune Pharmacol. 2012 Mar;7(1):113-39. doi: 10.1007/s11481-011-9288-1. Epub 2011 Jul 5.

DOI:10.1007/s11481-011-9288-1
PMID:21728034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3280383/
Abstract

Methamphetamine (METH) is a frequent drug of abuse in U.S. populations and commonly associated with psychosis. This may be a factor in frequent criminal justice referrals and lengthy treatment required by METH users. Persecutory delusions and auditory hallucinations are the most consistent symptoms of METH-associated psychosis (MAP). MAP has largely been studied in Asian populations and risk factors have varied across studies. Duration, frequency and amount of use as well as sexual abuse, family history, other substance use, and co-occurring personality and mood disorders are risk factors for MAP. MAP may be unique with its long duration of psychosis and recurrence without relapse to METH. Seven candidate genes have been identified that may be associated with MAP. Six of these genes are also associated with susceptibility, symptoms, or treatment of schizophrenia and most are linked to glutamatergic neurotransmission. Animal studies of pre-pulse inhibition, attenuation of social interaction, and stereotypy and alterations in locomotion are used to study MAP in rodents. Employing various models, rodent studies have identified neuroanatomical and neurochemical changes associated with METH use. Throughout this review, we identify key gaps in our understanding of MAP and suggest potential directions for future research.

摘要

甲基苯丙胺(METH)是美国人群中常见的滥用药物,通常与精神病有关。这可能是 METH 用户经常被转介到刑事司法系统和需要接受长时间治疗的一个因素。迫害妄想和幻听是与 METH 相关的精神病(MAP)最常见的症状。MAP 主要在亚洲人群中进行了研究,不同的研究有不同的风险因素。使用的持续时间、频率和数量,以及性虐待、家族史、其他物质使用,以及同时存在的人格和情绪障碍,都是 MAP 的风险因素。MAP 可能具有独特的特点,即精神病持续时间长,且不会因 METH 复发而复发。已经确定了七个可能与 MAP 相关的候选基因。其中六个基因也与精神分裂症的易感性、症状或治疗有关,大多数与谷氨酸能神经传递有关。动物研究中的预脉冲抑制、社交互动减弱、刻板行为和运动行为改变,用于在啮齿动物中研究 MAP。通过各种模型,啮齿动物研究已经确定了与 METH 使用相关的神经解剖学和神经化学变化。在整篇综述中,我们确定了对 MAP 理解的关键差距,并提出了未来研究的潜在方向。