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1
Autism severity is associated with child and maternal MAOA genotypes.自闭症严重程度与儿童和母亲的 MAOA 基因型有关。
Clin Genet. 2011 Apr;79(4):355-62. doi: 10.1111/j.1399-0004.2010.01471.x.
2
Behavioral disinhibition and reduced anxiety-like behaviors in monoamine oxidase B-deficient mice.单胺氧化酶 B 缺陷型小鼠的行为抑制缺失和焦虑样行为减少。
Neuropsychopharmacology. 2009 Dec;34(13):2746-57. doi: 10.1038/npp.2009.118. Epub 2009 Aug 26.
3
Simple behavioral assessment of mouse olfaction.小鼠嗅觉的简单行为评估。
Curr Protoc Neurosci. 2009 Jul;Chapter 8:Unit 8.24. doi: 10.1002/0471142301.ns0824s48.
4
Emotional face processing in schizophrenia.精神分裂症中的情绪面孔加工
Curr Opin Psychiatry. 2009 Mar;22(2):140-6. doi: 10.1097/YCO.0b013e328324f895.
5
Dysfunctional, but not functional, impulsivity is associated with a history of seriously violent behaviour and reduced orbitofrontal and hippocampal volumes in schizophrenia.功能失调而非功能正常的冲动性与精神分裂症患者严重暴力行为史以及眶额皮质和海马体体积减小有关。
Psychiatry Res. 2009 Jul 15;173(1):39-44. doi: 10.1016/j.pscychresns.2008.09.003. Epub 2009 May 12.
6
A polymorphism of the MAOA gene is associated with emotional brain markers and personality traits on an antisocial index.单胺氧化酶A(MAOA)基因的多态性与反社会指数上的情绪脑标记物及人格特质相关。
Neuropsychopharmacology. 2009 Jun;34(7):1797-809. doi: 10.1038/npp.2009.1. Epub 2009 Feb 4.
7
Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean.韩国人群中基于家庭和群体的单胺氧化酶A与自闭症谱系障碍的关联研究。
Neurosci Res. 2009 Mar;63(3):172-6. doi: 10.1016/j.neures.2008.11.007. Epub 2008 Nov 30.
8
Dynamic activation of the anterior cingulate cortex during anticipatory anxiety.预期性焦虑期间前扣带回皮层的动态激活
Neuroimage. 2009 Feb 1;44(3):975-81. doi: 10.1016/j.neuroimage.2008.10.022. Epub 2008 Nov 5.
9
HPA axis function in male caregivers: effect of the monoamine oxidase-A gene promoter (MAOA-uVNTR).男性照料者的下丘脑-垂体-肾上腺轴功能:单胺氧化酶A基因启动子(MAOA-uVNTR)的作用
Biol Psychol. 2008 Oct;79(2):250-5. doi: 10.1016/j.biopsycho.2008.06.004. Epub 2008 Jul 1.
10
The elevated T-maze as a measure of two types of defensive reactions: a factor analysis.作为两种防御反应测量手段的高架T型迷宫:一项因素分析
Brain Res Bull. 2008 Jul 1;76(4):376-9. doi: 10.1016/j.brainresbull.2008.03.016. Epub 2008 Apr 23.

单胺氧化酶 A 缺陷型小鼠的适应性防御行为。

Maladaptive defensive behaviours in monoamine oxidase A-deficient mice.

机构信息

Department of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90089, USA.

出版信息

Int J Neuropsychopharmacol. 2011 Oct;14(9):1195-207. doi: 10.1017/S1461145710001483. Epub 2010 Dec 15.

DOI:10.1017/S1461145710001483
PMID:21156093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3435117/
Abstract

Rich evidence indicates that monoamine oxidase (MAO) A, the major enzyme catalysing the degradation of monoamine neurotransmitters, plays a key role in emotional regulation. Although MAOA deficiency is associated with reactive aggression in humans and mice, the involvement of this enzyme in defensive behaviour remains controversial and poorly understood. To address this issue, we tested MAOA knockout (KO) mice in a spectrum of paradigms and settings associated with variable degrees of threat. The presentation of novel inanimate objects induced a significant reduction in exploratory approaches and increase in defensive behaviours, such as tail-rattling, biting and digging. These neophobic responses were context-dependent and particularly marked in the home cage. In the elevated plus- and T-mazes, MAOA KO mice and wild-type (WT) littermates displayed equivalent locomotor activity and time in closed and open arms; however, MAOA KO mice featured significant reductions in risk assessment, as well as unconditioned avoidance and escape. No differences between genotypes were observed in the defensive withdrawal and emergence test. Conversely, MAOA KO mice exhibited a dramatic reduction of defensive and fear-related behaviours in the presence of predator-related cues, such as predator urine or an anaesthetized rat, in comparison with those observed in their WT littermates. The behavioural abnormalities in MAOA KO mice were not paralleled by overt alterations in sensory and microvibrissal functions. Collectively, these results suggest that MAOA deficiency leads to a general inability to appropriately assess contextual risk and attune defensive and emotional responses to environmental cues.

摘要

大量证据表明,单胺氧化酶(MAO)A 是主要的单胺神经递质降解酶,在情绪调节中发挥关键作用。尽管 MAOA 缺乏与人类和小鼠的反应性攻击有关,但该酶在防御行为中的参与仍存在争议且了解甚少。为了解决这个问题,我们在与威胁程度不同的各种范式和环境中测试了 MAOA 敲除(KO)小鼠。新的无生命物体的呈现导致探索行为显著减少,防御行为增加,例如尾巴抖动、咬和挖。这些对新事物的恐惧反应是上下文相关的,在家庭笼中尤为明显。在高架十字迷宫和 T 迷宫中,MAOA KO 小鼠和野生型(WT)同窝仔鼠表现出相当的运动活性和在封闭臂和开放臂中的时间;然而,MAOA KO 小鼠的风险评估、无条件回避和逃避显著减少。在防御性回避和出现测试中,两种基因型之间没有差异。相反,与 WT 同窝仔鼠相比,MAOA KO 小鼠在存在与捕食者相关的线索(如捕食者尿液或麻醉大鼠)时,表现出防御和恐惧相关行为的急剧减少。MAOA KO 小鼠的行为异常与感觉和微触须功能的明显改变不平行。总的来说,这些结果表明 MAOA 缺乏导致对环境风险的整体评估能力降低,以及对环境线索的防御和情绪反应失调。