• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

单胺氧化酶 A 启动子区 VNTR 多态性与法医尸检病例中脑脊液儿茶酚胺浓度的关系。

VNTR polymorphism in the monoamine oxidase A promoter region and cerebrospinal fluid catecholamine concentrations in forensic autopsy cases.

机构信息

Department of Forensic Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.

Department of Forensic Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.

出版信息

Neurosci Lett. 2019 May 14;701:71-76. doi: 10.1016/j.neulet.2019.02.029. Epub 2019 Feb 19.

DOI:10.1016/j.neulet.2019.02.029
PMID:30794821
Abstract

Monoamine oxidase A (MAOA) plays important roles in the metabolism of catecholamines and modulates adrenergic, noradrenergic, and dopaminergic signaling. A polymorphic promoter variable number tandem repeat (VNTR) locus (MAOA-uVNTR) is located approximately 1.2 kb upstream from MAOA exon 1. Functional studies revealed that MAOA-uVNTR affects gene expression. In the present study, we examined the frequencies of MAOA-uVNTR alleles in Japanese autopsy cases, in which amphetamines or psychotropic drugs were not detected. In total, 87 males and 35 females were evaluated and investigated for the possible effect of MAOA-uVNTR polymorphisms on cerebrospinal fluid (CSF) catecholamine concentrations. In males, there was no significant association between MAOA-uVNTR polymorphisms and CSF adrenaline (Adr), noradrenaline (Nad), or dopamine (DA) levels. In contrast, females who were homozygous for the 3-repeat allele (i.e., 3/3 genotype carriers) had higher CSF levels of Adr (p =  0.024) and DA (p =  0.035) than individuals who were heterozygous or homozygous for the 4-repeat allele (3/4 and 4/4, respectively). We found no significant association between MAOA-uVNTR polymorphisms and CSF Nad levels in females. Thus, the results of the present study indicated that MAOA-uVNTR polymorphism influences CSF Adr and DA levels in females.

摘要

单胺氧化酶 A(MAOA)在儿茶酚胺的代谢中发挥重要作用,并调节肾上腺素能、去甲肾上腺素能和多巴胺能信号。一个多态性启动子可变数串联重复(VNTR)基因座(MAOA-uVNTR)位于 MAOA 外显子 1 的上游约 1.2kb 处。功能研究表明,MAOA-uVNTR 影响基因表达。在本研究中,我们检查了日本尸检病例中 MAOA-uVNTR 等位基因的频率,其中未检测到安非他命或精神药物。总共评估了 87 名男性和 35 名女性,并研究了 MAOA-uVNTR 多态性对脑脊液(CSF)儿茶酚胺浓度的可能影响。在男性中,MAOA-uVNTR 多态性与 CSF 肾上腺素(Adr)、去甲肾上腺素(Nad)或多巴胺(DA)水平之间没有显著关联。相比之下,纯合 3 重复等位基因(即 3/3 基因型携带者)的女性 CSF 中 Adr(p=0.024)和 DA(p=0.035)水平高于杂合或纯合 4 重复等位基因(3/4 和 4/4,分别)的个体。我们在女性中未发现 MAOA-uVNTR 多态性与 CSF Nad 水平之间存在显著关联。因此,本研究的结果表明,MAOA-uVNTR 多态性影响女性 CSF Adr 和 DA 水平。

相似文献

1
VNTR polymorphism in the monoamine oxidase A promoter region and cerebrospinal fluid catecholamine concentrations in forensic autopsy cases.单胺氧化酶 A 启动子区 VNTR 多态性与法医尸检病例中脑脊液儿茶酚胺浓度的关系。
Neurosci Lett. 2019 May 14;701:71-76. doi: 10.1016/j.neulet.2019.02.029. Epub 2019 Feb 19.
2
Association between serum catecholamine levels and VNTR polymorphism in the promoter region of the monoamine oxidase A gene in forensic autopsy cases.法医尸检案例中血清儿茶酚胺水平与单胺氧化酶 A 基因启动子区 VNTR 多态性的关联。
Leg Med (Tokyo). 2024 Sep;70:102469. doi: 10.1016/j.legalmed.2024.102469. Epub 2024 Jun 6.
3
No evidence of an association between a functional monoamine oxidase a gene polymorphism and completed suicides.无证据表明功能性单胺氧化酶A基因多态性与自杀身亡之间存在关联。
Am J Med Genet. 2002 Apr 8;114(3):340-2. doi: 10.1002/ajmg.10237.
4
Associations of a regulatory polymorphism of monoamine oxidase-A gene promoter (MAOA-uVNTR) with symptoms of depression and sleep quality.单胺氧化酶A基因启动子调节多态性(MAOA-uVNTR)与抑郁症状和睡眠质量的关联。
Psychosom Med. 2007 Jun;69(5):396-401. doi: 10.1097/PSY.0b013e31806d040b.
5
Possible interaction between MAOA and DRD2 genes associated with antisocial alcoholism among Han Chinese men in Taiwan.台湾汉族男性中与反社会型酒精中毒相关的单胺氧化酶A(MAOA)基因和多巴胺D2受体(DRD2)基因之间可能存在的相互作用。
Prog Neuropsychopharmacol Biol Psychiatry. 2007 Jan 30;31(1):108-14. doi: 10.1016/j.pnpbp.2006.08.010. Epub 2006 Sep 27.
6
Lipid levels are associated with a regulatory polymorphism of the monoamine oxidase-A gene promoter (MAOA-uVNTR).血脂水平与单胺氧化酶A基因启动子(MAOA-uVNTR)的一个调控多态性相关。
Med Sci Monit. 2008 Feb;14(2):CR57-61.
7
MAOA-uVNTR polymorphism in a Brazilian sample: further support for the association with impulsive behaviors and alcohol dependence.巴西样本中的单胺氧化酶A基因可变数目串联重复序列多态性:对其与冲动行为及酒精依赖关联的进一步支持
Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):305-8. doi: 10.1002/ajmg.b.30290.
8
An association between a functional polymorphism in the monoamine oxidase a gene promoter, impulsive traits and early abuse experiences.单胺氧化酶A基因启动子区功能性多态性、冲动特质与早期虐待经历之间的关联。
Neuropsychopharmacology. 2004 Aug;29(8):1498-505. doi: 10.1038/sj.npp.1300455.
9
A regulatory polymorphism of the monoamine oxidase-A gene may be associated with variability in aggression, impulsivity, and central nervous system serotonergic responsivity.单胺氧化酶A基因的一种调节性多态性可能与攻击性、冲动性及中枢神经系统血清素反应性的变异性有关。
Psychiatry Res. 2000 Jul 24;95(1):9-23. doi: 10.1016/s0165-1781(00)00162-1.
10
Associations Between MAOA-uVNTR Genotype, Maltreatment, MAOA Methylation, and Alcohol Consumption in Young Adult Males.MAOA-uVNTR 基因型、虐待、MAOA 甲基化与青年男性饮酒之间的关联。
Alcohol Clin Exp Res. 2018 Mar;42(3):508-519. doi: 10.1111/acer.13578. Epub 2018 Jan 31.

引用本文的文献

1
Monoamine oxidase-A (MAO-A) low-expression variants and increased risk of Plasmodium vivax malaria relapses.单胺氧化酶-A(MAO-A)低表达变体与间日疟复发风险增加相关。
J Antimicrob Chemother. 2024 Aug 1;79(8):1985-1989. doi: 10.1093/jac/dkae196.
2
Genetic Variant and Major Depressive Disorder: A Systematic Review.遗传变异与重度抑郁症:系统评价。
Cells. 2022 Oct 17;11(20):3267. doi: 10.3390/cells11203267.
3
The presence of polymorphisms in genes controlling neurotransmitter metabolism and disease prognosis in patients with prostate cancer: a possible link with schizophrenia.
前列腺癌患者中控制神经递质代谢的基因多态性与疾病预后的关系:与精神分裂症的可能联系。
Oncotarget. 2021 Mar 30;12(7):698-707. doi: 10.18632/oncotarget.27921.