• 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

在健康志愿者中,停止信号反应抑制不受色氨酸耗竭或5-羟色胺转运体多态性的调节:对冲动性的5-羟色胺理论的启示。

Stop signal response inhibition is not modulated by tryptophan depletion or the serotonin transporter polymorphism in healthy volunteers: implications for the 5-HT theory of impulsivity.

作者信息

Clark L, Roiser J P, Cools R, Rubinsztein D C, Sahakian B J, Robbins T W

机构信息

Department of Experimental Psychology, University of Cambridge, Downing Street, and Department of Medical Genetics, Addenbrooke's Hospital, Cambridge, UK.

出版信息

Psychopharmacology (Berl). 2005 Nov;182(4):570-8. doi: 10.1007/s00213-005-0104-6. Epub 2005 Oct 19.

DOI:10.1007/s00213-005-0104-6
PMID:16163530
Abstract

RATIONALE

Reduced serotonin neurotransmission is implicated in disorders of impulse control, but the involvement of serotonin in inhibitory processes in healthy human subjects remains unclear.

OBJECTIVES

To investigate the effects of an acute manipulation of serotonin and genotype at a functional polymorphism in a gene coding for the serotonin transporter (5-HTT) on an established measure of response inhibition.

METHODS

Serotonin function was reduced by the acute tryptophan depletion (ATD) procedure in a double-blind, crossover design in 42 healthy subjects. The Stop Signal Task (SST) was administered 5-7 h after drink administration. The influences of 5-HTT polymorphism, gender and trait impulsivity were investigated.

RESULTS

ATD was associated with significant depletion of plasma tryptophan levels but did not increase the stop signal reaction time in comparison to the balanced (placebo) amino acid mixture. Subjects possessing the short allele of the 5-HTT polymorphism were not more impulsive on the SST than subjects homozygous for the long allele under placebo conditions and were not disproportionately sensitive to the effects of ATD. There was no effect of gender or trait impulsivity on ATD-induced change.

CONCLUSIONS

We find no support for the involvement of brain serotonin neurotransmission in this form of inhibitory control in healthy human subjects.

摘要

理论依据

血清素神经传递减少与冲动控制障碍有关,但血清素在健康人类受试者抑制过程中的作用仍不清楚。

目的

研究血清素的急性调控以及血清素转运体(5-HTT)编码基因功能多态性的基因型对既定反应抑制测量指标的影响。

方法

在42名健康受试者中采用双盲交叉设计,通过急性色氨酸耗竭(ATD)程序降低血清素功能。饮用饮料5 - 7小时后进行停止信号任务(SST)。研究了5-HTT多态性、性别和特质冲动性的影响。

结果

与平衡(安慰剂)氨基酸混合物相比,ATD与血浆色氨酸水平的显著降低有关,但并未增加停止信号反应时间。在安慰剂条件下,具有5-HTT多态性短等位基因的受试者在SST上并不比长等位基因纯合子受试者更冲动,且对ATD的影响也没有过度敏感。性别或特质冲动性对ATD诱导的变化没有影响。

结论

我们没有发现证据支持脑血清素神经传递参与健康人类受试者这种形式的抑制控制。

相似文献

1
Stop signal response inhibition is not modulated by tryptophan depletion or the serotonin transporter polymorphism in healthy volunteers: implications for the 5-HT theory of impulsivity.在健康志愿者中,停止信号反应抑制不受色氨酸耗竭或5-羟色胺转运体多态性的调节:对冲动性的5-羟色胺理论的启示。
Psychopharmacology (Berl). 2005 Nov;182(4):570-8. doi: 10.1007/s00213-005-0104-6. Epub 2005 Oct 19.
2
Tryptophan depletion disrupts the motivational guidance of goal-directed behavior as a function of trait impulsivity.色氨酸耗竭会破坏作为特质冲动性函数的目标导向行为的动机引导。
Neuropsychopharmacology. 2005 Jul;30(7):1362-73. doi: 10.1038/sj.npp.1300704.
3
Interactive effects of sex and 5-HTTLPR on mood and impulsivity during tryptophan depletion in healthy people.性别与5-羟色胺转运体基因连锁多态性区域(5-HTTLPR)在健康人群色氨酸耗竭期间对情绪和冲动性的交互作用。
Biol Psychiatry. 2007 Sep 15;62(6):593-9. doi: 10.1016/j.biopsych.2007.02.012. Epub 2007 Jun 4.
4
The short (S) allele of the serotonin transporter polymorphism and acute tryptophan depletion both increase impulsivity in men.短(S)等位基因的血清素转运体多态性和急性色氨酸耗竭都会增加男性的冲动性。
Neurosci Lett. 2010 Apr 12;473(3):208-11. doi: 10.1016/j.neulet.2010.02.048. Epub 2010 Feb 25.
5
Serotonin transporter polymorphism mediates vulnerability to loss of incentive motivation following acute tryptophan depletion.血清素转运体基因多态性介导了急性色氨酸耗竭后动机激励缺失的易感性。
Neuropsychopharmacology. 2006 Oct;31(10):2264-72. doi: 10.1038/sj.npp.1301055. Epub 2006 Mar 15.
6
The effects of acute tryptophan depletion and serotonin transporter polymorphism on emotional processing in memory and attention.急性色氨酸耗竭和5-羟色胺转运体基因多态性对记忆与注意力中情绪加工的影响。
Int J Neuropsychopharmacol. 2007 Aug;10(4):449-61. doi: 10.1017/S146114570600705X. Epub 2006 Aug 8.
7
Effects of serotonin depletion on punishment processing in the orbitofrontal and anterior cingulate cortices of healthy women.血清素耗竭对健康女性眶额皮质和前扣带回皮质中惩罚处理的影响。
Eur Neuropsychopharmacol. 2015 Jun;25(6):846-56. doi: 10.1016/j.euroneuro.2015.02.007. Epub 2015 Feb 28.
8
The effect of acute tryptophan depletion on the BOLD response during performance monitoring and response inhibition in healthy male volunteers.急性色氨酸耗竭对健康男性志愿者在执行监测和反应抑制过程中脑血流动力学反应的影响。
Psychopharmacology (Berl). 2006 Aug;187(2):200-8. doi: 10.1007/s00213-006-0411-6. Epub 2006 May 19.
9
Differential effect of the 5-HTT gene-linked polymorphic region on emotional eating during stress exposure following tryptophan challenge.色氨酸挑战后应激暴露期间 5-HTT 基因连锁多态区对情绪性进食的差异影响。
J Nutr Biochem. 2012 Apr;23(4):410-6. doi: 10.1016/j.jnutbio.2011.01.005. Epub 2011 Jun 11.
10
The role of 5-HTTLPR in choosing the lesser of two evils, the better of two goods: examining the impact of 5-HTTLPR genotype and tryptophan depletion in object choice.5-羟色胺转运体基因连锁多态性区域(5-HTTLPR)在两害相权取其轻、两利相权取其重中的作用:研究5-HTTLPR基因型和色氨酸耗竭对客体选择的影响。
Psychopharmacology (Berl). 2008 Jan;196(1):29-38. doi: 10.1007/s00213-007-0920-y. Epub 2007 Oct 17.

引用本文的文献

1
Investigating Ecological Momentary Assessed Physical Activity and Core Executive Functions in 18- to 24-Year-Old Undergraduate Students.探究 18 至 24 岁大学生的生态瞬时评估体力活动与核心执行功能。
Int J Environ Res Public Health. 2023 Oct 19;20(20):6944. doi: 10.3390/ijerph20206944.
2
A Role for Serotonin in Modulating Opposing Drive and Brake Circuits of Impulsivity.血清素在调节冲动的对立驱动和制动回路中的作用。
Front Behav Neurosci. 2022 Feb 17;16:791749. doi: 10.3389/fnbeh.2022.791749. eCollection 2022.
3
Neuromodulation of prefrontal cortex cognitive function in primates: the powerful roles of monoamines and acetylcholine.

本文引用的文献

1
Tryptophan depletion reduces right inferior prefrontal activation during response inhibition in fast, event-related fMRI.在快速事件相关功能磁共振成像(fMRI)的反应抑制过程中,色氨酸耗竭会降低右下前额叶的激活。
Psychopharmacology (Berl). 2005 Jun;179(4):791-803. doi: 10.1007/s00213-004-2116-z. Epub 2005 Jan 26.
2
Tryptophan depletion disrupts the motivational guidance of goal-directed behavior as a function of trait impulsivity.色氨酸耗竭会破坏作为特质冲动性函数的目标导向行为的动机引导。
Neuropsychopharmacology. 2005 Jul;30(7):1362-73. doi: 10.1038/sj.npp.1300704.
3
A functional genetic variation of the serotonin (5-HT) transporter affects 5-HT1A receptor binding in humans.
灵长类动物前额叶皮质认知功能的神经调节:单胺类和乙酰胆碱的重要作用。
Neuropsychopharmacology. 2022 Jan;47(1):309-328. doi: 10.1038/s41386-021-01100-8. Epub 2021 Jul 26.
4
The Role of Tryptophan and Tyrosine in Executive Function and Reward Processing.色氨酸和酪氨酸在执行功能及奖赏处理中的作用
Int J Tryptophan Res. 2020 Oct 22;13:1178646920964825. doi: 10.1177/1178646920964825. eCollection 2020.
5
Rejecting impulsivity as a psychological construct: A theoretical, empirical, and sociocultural argument.拒绝冲动作为一种心理结构:理论、实证和社会文化的论证。
Psychol Rev. 2021 Mar;128(2):336-361. doi: 10.1037/rev0000263. Epub 2020 Sep 24.
6
Which came first: Cannabis use or deficits in impulse control?是先有大麻使用还是冲动控制缺陷?
Prog Neuropsychopharmacol Biol Psychiatry. 2021 Mar 2;106:110066. doi: 10.1016/j.pnpbp.2020.110066. Epub 2020 Aug 11.
7
Impact of Polymorphisms in the Serotonin Transporter Gene on Oscillatory Dynamics during Inhibition of Planned Movement in Children.血清素转运体基因多态性对儿童计划运动抑制过程中振荡动力学的影响。
Brain Sci. 2019 Nov 6;9(11):311. doi: 10.3390/brainsci9110311.
8
Dissociable effects of acute SSRI (escitalopram) on executive, learning and emotional functions in healthy humans.急性 SSRI(依他普仑)对健康人类执行功能、学习功能和情绪功能的可分离影响。
Neuropsychopharmacology. 2018 Dec;43(13):2645-2651. doi: 10.1038/s41386-018-0229-z. Epub 2018 Sep 26.
9
Mapping Compulsivity in the DSM-5 Obsessive Compulsive and Related Disorders: Cognitive Domains, Neural Circuitry, and Treatment.DSM-5 强迫及相关障碍中的强迫映射:认知领域、神经回路和治疗。
Int J Neuropsychopharmacol. 2018 Jan 1;21(1):42-58. doi: 10.1093/ijnp/pyx088.
10
Prefrontal cortex executive processes affected by stress in health and disease.前额皮质执行功能在健康和疾病中的应激影响。
Prog Neuropsychopharmacol Biol Psychiatry. 2018 Jul 13;85:161-179. doi: 10.1016/j.pnpbp.2017.07.004. Epub 2017 Jul 6.
血清素(5-羟色胺,5-HT)转运体的功能性基因变异会影响人类体内5-HT1A受体的结合。
J Neurosci. 2005 Mar 9;25(10):2586-90. doi: 10.1523/JNEUROSCI.3769-04.2005.
4
The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder.样本量和同质抽样的作用:5-羟色胺转运体基因连锁多态性与重度抑郁症之间的关联
Biol Psychiatry. 2005 Feb 1;57(3):247-51. doi: 10.1016/j.biopsych.2004.11.027.
5
Serotonergic modulation of prefrontal cortex during negative feedback in probabilistic reversal learning.概率性逆转学习中负反馈期间前额叶皮层的5-羟色胺能调节
Neuropsychopharmacology. 2005 Jun;30(6):1138-47. doi: 10.1038/sj.npp.1300663.
6
Cognitive inflexibility after prefrontal serotonin depletion.前额叶5-羟色胺耗竭后的认知灵活性障碍
Science. 2004 May 7;304(5672):878-80. doi: 10.1126/science.1094987.
7
Fractionating impulsivity: contrasting effects of central 5-HT depletion on different measures of impulsive behavior.冲动性的细分:中枢5-羟色胺耗竭对不同冲动行为测量指标的对比影响。
Neuropsychopharmacology. 2004 Jul;29(7):1331-43. doi: 10.1038/sj.npp.1300434.
8
Cognitive changes after acute tryptophan depletion: what can they tell us?急性色氨酸耗竭后的认知变化:它们能告诉我们什么?
Psychol Med. 2004 Jan;34(1):3-8. doi: 10.1017/s0033291703008924.
9
Methylphenidate improves response inhibition in adults with attention-deficit/hyperactivity disorder.哌甲酯可改善患有注意力缺陷多动障碍的成年人的反应抑制能力。
Biol Psychiatry. 2003 Dec 15;54(12):1465-8. doi: 10.1016/s0006-3223(03)00609-7.
10
Inhibitory control in rats performing a stop-signal reaction-time task: effects of lesions of the medial striatum and d-amphetamine.大鼠执行停止信号反应时任务中的抑制控制:内侧纹状体损伤和右旋苯丙胺的影响
Behav Neurosci. 2003 Dec;117(6):1302-17. doi: 10.1037/0735-7044.117.6.1302.