Department of Clinical and Experimental Medicine, Pharmacology Section, Via Fossato di Mortara 17-19, 44100, Ferrara, Italy.
Curr Med Chem. 2012;19(3):304-16. doi: 10.2174/092986712803414268.
The existence of functional NT/dopamine interactions in the central nervous system has been extensively documented. Among others, a possible molecular mechanism underlying the NT-induced modulation of dopamine release is a direct antagonistic NTS(1)/D(2) receptor interaction. More recently, neurochemical experiments also supported the existence of a possible interaction between NT and N-methyl-d-aspartate (NMDA) receptors. In particular, it has been suggested that NT, by amplifying NMDA receptor signaling, could be involved in neurodegeneration. The present article attempts to provide a summary of current knowledge, mainly emerging from our studies, on the existence of receptor-receptor interactions between NT receptor subtype 1 (NTS1) and dopamine D(2) or NMDA receptors in the brain. Special emphasis is placed on the pre and post-synaptic neurochemical mechanisms possibly underlying the involvement of these interactions in the physiopathology of schizophrenia and acute neurodegenerative disorders.
中枢神经系统中功能性 NT/多巴胺相互作用的存在已得到广泛证实。其中,NT 诱导的多巴胺释放调制的一个可能的分子机制是直接拮抗的 NTS(1)/D(2)受体相互作用。最近,神经化学实验也支持 NT 与 N-甲基-D-天冬氨酸 (NMDA) 受体之间可能存在相互作用。特别是,有人提出,NT 通过放大 NMDA 受体信号,可能参与神经退行性变。本文试图提供对当前知识的总结,主要来自我们的研究,关于 NT 受体亚型 1 (NTS1) 和多巴胺 D(2)或 NMDA 受体之间受体-受体相互作用在精神分裂症和急性神经退行性疾病的病理生理学中的存在。特别强调了这些相互作用可能参与精神分裂症和急性神经退行性疾病的病理生理学的突触前和突触后神经化学机制。