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多动小鼠中血清素/多巴胺的相互作用:血清素受体1B活性降低可逆转多巴胺转运体基因敲除的影响。

Serotonin/dopamine interactions in a hyperactive mouse: reduced serotonin receptor 1B activity reverses effects of dopamine transporter knockout.

作者信息

Hall Frank Scott, Sora Ichiro, Hen René, Uhl George R

机构信息

Department of Pharmacology, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, Ohio, United States of America; Molecular Neurobiology Branch, National Institute on Drug Abuse - Intramural Research Program, Baltimore, Maryland, United States of America.

Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

PLoS One. 2014 Dec 16;9(12):e115009. doi: 10.1371/journal.pone.0115009. eCollection 2014.

Abstract

Knockout (KO) mice that lack the dopamine transporter (SL6A3; DAT) display increased locomotion that can be attenuated, under some circumstances, by administration of drugs that normally produce psychostimulant-like effects, such as amphetamine and methylphenidate. These results have led to suggestions that DAT KO mice may model features of attention deficit hyperactivity disorder (ADHD) and that these drugs may act upon serotonin (5-HT) systems to produce these unusual locomotor decreasing effects. Evidence from patterns of brain expression and initial pharmacologic studies led us to use genetic and pharmacologic approaches to examine the influence of altered 5-HT1B receptor activity on hyperactivity in DAT KO mice. Heterozygous 5-HT1B KO and pharmacologic 5-HT1B antagonism both attenuated locomotor hyperactivity in DAT KO mice. Furthermore, DAT KO mice with reduced, but not eliminated, 5-HT1B receptor expression regained cocaine-stimulated locomotion, which was absent in DAT KO mice with normal levels of 5-HT1B receptor expression. Further experiments demonstrated that the degree of habituation to the testing apparatus determined whether cocaine had no effect on locomotion in DAT KO or reduced locomotion, helping to resolve differences among prior reports. These findings of complementation of the locomotor effects of DAT KO by reducing 5-HT1B receptor activity underscore roles for interactions between specific 5-HT receptors and dopamine (DA) systems in basal and cocaine-stimulated locomotion and support evaluation of 5-HT1B antagonists as potential, non-stimulant ADHD therapeutics.

摘要

缺乏多巴胺转运体(SLC6A3;DAT)的基因敲除(KO)小鼠表现出运动增加,在某些情况下,给予通常产生类似精神兴奋剂作用的药物(如苯丙胺和哌甲酯)可使其运动增加得到减弱。这些结果表明,DAT基因敲除小鼠可能模拟注意力缺陷多动障碍(ADHD)的特征,并且这些药物可能作用于5-羟色胺(5-HT)系统以产生这些不寻常的运动减少效应。来自脑表达模式和初步药理学研究的证据促使我们使用遗传学和药理学方法来研究5-HT1B受体活性改变对DAT基因敲除小鼠多动的影响。杂合5-HT1B基因敲除和药理学上的5-HT1B拮抗作用均减弱了DAT基因敲除小鼠的运动性多动。此外,5-HT1B受体表达降低但未消除的DAT基因敲除小鼠恢复了可卡因刺激的运动,而5-HT1B受体表达正常的DAT基因敲除小鼠则没有这种运动。进一步的实验表明,对测试装置的习惯化程度决定了可卡因对DAT基因敲除小鼠的运动是没有影响还是减少运动,这有助于解决先前报告之间的差异。通过降低5-HT1B受体活性来补充DAT基因敲除的运动效应的这些发现强调了特定5-HT受体与多巴胺(DA)系统之间的相互作用在基础运动和可卡因刺激的运动中的作用,并支持将5-HT1B拮抗剂作为潜在的非兴奋剂ADHD治疗药物进行评估。

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