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Behav Brain Res. 2009 Jun 8;200(1):113-6. doi: 10.1016/j.bbr.2009.01.002. Epub 2009 Jan 8.
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Nitric oxide synthase inhibition attenuates phencyclidine-induced disruption of cognitive flexibility.一氧化氮合酶抑制可减轻苯环利定引起的认知灵活性破坏。
Pharmacol Biochem Behav. 2008 May;89(3):352-9. doi: 10.1016/j.pbb.2008.01.011. Epub 2008 Jan 26.
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Association of functional polymorphisms in NOS1 and NOS3 with loudness dependence of auditory evoked potentials.一氧化氮合酶1(NOS1)和一氧化氮合酶3(NOS3)功能多态性与听觉诱发电位响度依赖性的关联。
Int J Neuropsychopharmacol. 2008 Jun;11(4):477-83. doi: 10.1017/S1461145708008420. Epub 2008 Feb 8.
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Neuropsychopharmacology. 2008 Jul;33(8):1874-83. doi: 10.1038/sj.npp.1301587. Epub 2007 Sep 26.
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Metabolic investigation in psychiatric disorders.精神疾病的代谢研究。
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10
Histamine h3 receptor antagonists potentiate methamphetamine self-administration and methamphetamine-induced accumbal dopamine release.组胺H3受体拮抗剂增强甲基苯丙胺的自我给药行为以及甲基苯丙胺诱导的伏隔核多巴胺释放。
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NOS3 基因与日本人群甲基苯丙胺所致精神分裂症的关联分析

Genetic Association Analysis of NOS3 and Methamphetamine-Induced Psychosis Among Japanese.

机构信息

Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan.

出版信息

Curr Neuropharmacol. 2011 Mar;9(1):151-4. doi: 10.2174/157015911795017119.

DOI:10.2174/157015911795017119
PMID:21886581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3137171/
Abstract

Endothelial nitric oxide synthase (NOS3) is one of the enzymes influencing nitric oxide (NO) function in the human brain. NO is a gaseous neurotransmitter that is involved in a variety of mechanisms in the central nervous system, such as N-methyl-D-aspartate receptor activation and oxidative stress. The evidence from animal pharmacological studies and postmortem studies supports an association between NO and psychotic disorders. Methamphetamine (METH) use disorder is a known psychotic disorder, and we therefore conducted a gene-based case-control study between tagging single nucleotide polymorphisms (SNPs) (rs2070744, rs1799983) in NOS3 and METH-induced psychosis in Japanese subjects (183 with METH-induced psychosis and 267 controls). Written informed consent was obtained from each subject. No significant association was found between any tagging SNP in NOS3 and METH-induced psychosis in the allele/genotype-wise or haplotype-wise analyses. In conclusion, we suggest that NOS3 might not contribute to the risk of METH-induced psychosis in the Japanese population.

摘要

内皮型一氧化氮合酶(NOS3)是影响人类大脑中一氧化氮(NO)功能的酶之一。NO 是一种气体神经递质,参与中枢神经系统的多种机制,如 N-甲基-D-天冬氨酸受体激活和氧化应激。动物药理学研究和尸检研究的证据支持 NO 与精神病障碍之间存在关联。甲基苯丙胺(METH)使用障碍是一种已知的精神病障碍,因此我们在日本受试者中进行了 NOS3 中的标记单核苷酸多态性(SNP)(rs2070744、rs1799983)与 METH 诱导的精神病之间的基于基因的病例对照研究(183 例 METH 诱导的精神病和 267 例对照)。每位受试者均获得书面知情同意。在等位基因/基因型或单体型分析中,NOS3 中的任何标记 SNP 与 METH 诱导的精神病之间均未发现显著关联。总之,我们认为 NOS3 可能不会增加日本人发生 METH 诱导的精神病的风险。