Department of Clinical and Experimental Medicine, Pharmacology Section, University of Ferrara, and IRET Foundation, Ozzano Emilia, Bologna, Italy.
Brain Res. 2012 Oct 2;1476:96-107. doi: 10.1016/j.brainres.2012.01.032. Epub 2012 Jan 24.
The present manuscript mainly summarizes the basic concepts and the molecular mechanisms underlying adenosine A(2A)-dopamine D(2) receptor-receptor interactions in the basal ganglia. Special emphasis is placed on neurochemical, behavioral and electrophysiological findings supporting the functional role that A(2A)/D(2) heteromeric receptor complexes located on striato-pallidal GABA neurons and corticostriatal glutamate terminals play in the regulation of the so called "basal ganglia indirect pathway". Furthermore, the role of A(2A)/mGluR(5) synergistic interactions in striatal neuron function and dysfunction is discussed. The functional consequences of the interactions between striatal adenosine A(2A), mGluR(5) and dopamine D(2) receptors on striatopallidal GABA release and motor behavior dysfunctions suggest the possibility of simultaneously targeting these receptors in Parkinson's disease treatment. This article is part of a Special Issue entitled Brain Integration. This article is part of a Special Issue entitled: Brain Integration.
本文主要总结了基底神经节中腺苷 A(2A)-多巴胺 D(2)受体-受体相互作用的基本概念和分子机制。特别强调了神经化学、行为和电生理学研究结果,这些结果支持位于纹状体-苍白球 GABA 神经元和皮质纹状体谷氨酸末端的 A(2A)/D(2)异源受体复合物在调节所谓的“基底神经节间接通路”中的功能作用。此外,还讨论了 A(2A)/mGluR(5)协同相互作用在纹状体神经元功能和功能障碍中的作用。纹状体腺苷 A(2A)、mGluR(5)和多巴胺 D(2)受体之间相互作用对纹状体-苍白球 GABA 释放和运动行为障碍的功能后果表明,在帕金森病治疗中同时靶向这些受体的可能性。本文是一个题为“大脑整合”的特刊的一部分。本文是一个题为“大脑整合”的特刊的一部分。