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间接基底神经节通路介导的重复行为:腺苷受体激动剂的抑制作用。

Indirect basal ganglia pathway mediation of repetitive behavior: attenuation by adenosine receptor agonists.

机构信息

Departments of Psychiatry and Psychology, McKnight Brain Institute, University of Florida, Gainesville, FL, United States.

出版信息

Behav Brain Res. 2010 Jun 26;210(1):116-22. doi: 10.1016/j.bbr.2010.02.030. Epub 2010 Feb 21.

Abstract

Repetitive behaviors are diagnostic for autism and common in related neurodevelopmental disorders. Despite their clinical importance, underlying mechanisms associated with the expression of these behaviors remain poorly understood. Our lab has previously shown that the rates of spontaneous stereotypy in deer mice (Peromyscus maniculatus) were negatively correlated with enkephalin content, a marker of striatopallidal but not striatonigral neurons. To investigate further the role of the indirect basal ganglia pathway, we examined neuronal activation of the subthalamic nucleus (STN) using cytochrome oxidase (CO) histochemistry in high- and low-stereotypy mice. CO activity in STN was significantly lower in high-stereotypy mice and negatively correlated with the frequency of stereotypy. In addition, exposure to environmental enrichment, which attenuated stereotypy, normalized the activity of STN. Co-administration of the adenosine A(2A) receptor agonist CGS21680 and the A(1) receptor agonist CPA attenuated stereotypy dose-dependently. The significant reduction associated with the lowest dose of the drug combination tested was due to its effects on mice with lower baseline levels of stereotypy. Higher doses of the drug combination were required to show robust behavioral effects, and presumably requisite activation of the indirect pathway, in high-stereotypy mice. These findings support that decreased indirect pathway activity is linked to the expression of high levels of stereotypy in deer mice and that striatal A(1) and A(2A) receptors may provide promising therapeutic targets for the treatment of repetitive behaviors in neurodevelopmental disorders.

摘要

重复行为是自闭症的诊断特征,在相关的神经发育障碍中也很常见。尽管它们具有临床重要性,但与这些行为表达相关的潜在机制仍知之甚少。我们的实验室之前已经表明,鹿鼠(Peromyscus maniculatus)自发刻板行为的发生率与脑啡肽含量呈负相关,脑啡肽是纹状体苍白球而不是纹状体黑质神经元的标志物。为了进一步研究间接基底神经节通路的作用,我们使用细胞色素氧化酶(CO)组织化学方法在高刻板行为和低刻板行为的小鼠中检查了丘脑下核(STN)的神经元激活。高刻板行为小鼠的 STN 中的 CO 活性显着降低,与刻板行为的频率呈负相关。此外,环境丰富暴露可以减轻刻板行为,使 STN 的活性正常化。腺苷 A(2A)受体激动剂 CGS21680 和 A(1)受体激动剂 CPA 的共同给药可剂量依赖性地减弱刻板行为。与测试的最低药物组合剂量相关的显着降低归因于其对刻板行为基线水平较低的小鼠的影响。需要更高剂量的药物组合才能在高刻板行为的小鼠中显示出强大的行为效果,并且可能需要间接途径的必需激活。这些发现支持间接途径活性降低与鹿鼠高水平刻板行为的表达有关,并且纹状体 A(1)和 A(2A)受体可能为治疗神经发育障碍中的重复行为提供有前途的治疗靶点。

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