Department of Basic Medical Science, School of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
Neurochem Int. 2013 Sep;63(3):195-200. doi: 10.1016/j.neuint.2013.06.006. Epub 2013 Jun 14.
Nogo receptors (NgRs) are a family of cell surface receptors that are broadly expressed in the mammalian brain. These receptors could serve as an inhibitory element in the regulation of activity-dependent axonal growth and spine and synaptic formation in the adult animal brain. Thus, through balancing the structural response to changing cellular and synaptic inputs, NgRs participate in constructing activity-dependent morphological plasticity. Psychostimulants have been well documented to induce morphological plasticity critical for addictive properties of stimulants, although underlying molecular mechanisms are poorly understood. In this study, we initiated a study to investigate the response of NgRs to a stimulant. We tested the effect of acute administration of amphetamine on protein expression of two principal NgR subtypes (NgR1 and NgR2) in the rat striatum, medial prefrontal cortex (mPFC) and hippocampus. We found that a single injection of amphetamine induced a rapid and time-dependent decrease in NgR1 and NgR2 expression in the striatum and mPFC. A relatively delayed and time-dependent decrease in expression of the two receptors was seen in the hippocampus. The drug-induced decrease in NgR1 and NgR2 expression in the three forebrain regions was dose-dependent. A behaviorally active dose of the drug was required to trigger a significant reduction in NgR1 and NgR2 expression. These data indicate that NgRs are subject to the regulation by the stimulant. Amphetamine exposure exerts the inhibitory modulation of basal NgR1 and NgR2 expression in the key structures of reward circuits in vivo.
神经生长抑制因子受体(NgRs)是一类广泛表达于哺乳动物大脑中的细胞表面受体。这些受体可能作为一种抑制性元件,参与调节成年动物大脑中活性依赖的轴突生长和棘突及突触的形成。因此,通过平衡对细胞和突触输入变化的结构反应,NgRs 参与构建活性依赖的形态可塑性。有充分的文献记录表明,精神兴奋剂可诱导对兴奋剂成瘾特性至关重要的形态可塑性,尽管其潜在的分子机制尚不清楚。在这项研究中,我们着手研究兴奋剂对 NgRs 的反应。我们测试了安非他命急性给药对大鼠纹状体、内侧前额叶皮层(mPFC)和海马中两种主要 NgR 亚型(NgR1 和 NgR2)蛋白表达的影响。我们发现,单次注射安非他命可诱导纹状体和 mPFC 中 NgR1 和 NgR2 表达的快速且时间依赖性下降。在海马体中,两种受体的表达呈相对延迟和时间依赖性下降。两种受体在三个前脑区域的药物诱导表达下降呈剂量依赖性。药物需要发挥行为活性作用才能触发 NgR1 和 NgR2 表达的显著减少。这些数据表明 NgRs 受到兴奋剂的调节。安非他命暴露对体内奖励回路关键结构中的基础 NgR1 和 NgR2 表达产生抑制性调节。