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腹侧被盖区多巴胺能神经元上谷氨酸能突触对急性注射苯丙胺的快速突触可塑性。

Rapid synaptic plasticity of glutamatergic synapses on dopamine neurons in the ventral tegmental area in response to acute amphetamine injection.

作者信息

Faleiro Lavina J, Jones Susan, Kauer Julie A

机构信息

Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University, Providence, RI 02912, USA.

出版信息

Neuropsychopharmacology. 2004 Dec;29(12):2115-25. doi: 10.1038/sj.npp.1300495.

Abstract

Drugs of abuse activate the reward circuitry of the mesocorticolimbic system, and it has been hypothesized that drug exposure triggers synaptic plasticity of glutamatergic synapses onto dopamine (DA) neurons of the ventral tegmental area. Here, we show that just a 2 h in vivo exposure to amphetamine is sufficient to potentiate these synapses, measured as an increase in the synaptic AMPAR/NMDAR ratio. We tested the prediction that an increase in GluR1-containing AMPA receptors would result in an increase in GluR1 homomeric receptors at synapses, but were unable to observe any evidence of the predicted rectification in DA neurons from animals treated with amphetamine. We also examined the possibility of increased AMPA receptor insertion in the membrane, but did not detect a significant increase in biotinylated surface GluR1. We conclude that amphetamine induces rapid changes in synaptic AMPAR/NMDAR ratios, suggesting that potentiation of glutamatergic synapses is a relatively early event in the series of neuroadaptations in response to drugs of abuse.

摘要

滥用药物会激活中脑皮质边缘系统的奖赏回路,并且据推测,药物暴露会触发腹侧被盖区多巴胺(DA)能神经元上谷氨酸能突触的突触可塑性。在此,我们表明,仅2小时的体内苯丙胺暴露就足以增强这些突触,这可通过突触AMPA受体/ NMDA受体比率的增加来衡量。我们测试了这样的预测,即含GluR1的AMPA受体增加会导致突触处GluR1同聚体受体增加,但未能在接受苯丙胺治疗的动物的DA神经元中观察到任何预测矫正的证据。我们还研究了AMPA受体插入细胞膜增加的可能性,但未检测到生物素化表面GluR1的显著增加。我们得出结论,苯丙胺会诱导突触AMPA受体/ NMDA受体比率的快速变化,这表明谷氨酸能突触的增强是对滥用药物的一系列神经适应性反应中相对较早的事件。

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