Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, Valderrebollo 5, 28031, Madrid, Spain.
Molecular Neurobiology Laboratory, Department of Biochemistry and Molecular Biology, Faculty of Biology, University of Barcelona, 08028, Barcelona, Spain.
Mol Neurobiol. 2016 Oct;53(8):5436-45. doi: 10.1007/s12035-015-9468-8. Epub 2015 Oct 9.
Dopamine receptors in striatum are important for healthy brain functioning and are the target of levodopa-based therapy in Parkinson's disease. Lateralization of dopaminergic neurotransmission in striata from different hemispheres occurs in patients, but also in healthy individuals. Our data show that the affinity of dopamine binding to dopamine D1 receptors is significantly higher in left than in right striatum. Analysis of data from radioligand binding to striatal samples from naïve, 6-hydroxydopamine lesioned, levodopa-treated and levodopa-induced dyskinetic rats shows differential receptor structure and gives hints on the causes of right/left lateralization of dopamine binding to striatal D1 receptors. Moreover, binding data showed loss of lateralization in levodopa (L-DOPA)-induced dyskinetic rats.
纹状体中的多巴胺受体对于大脑的健康功能非常重要,也是帕金森病中左旋多巴治疗的靶点。来自不同半球的纹状体中的多巴胺能神经传递的偏侧化不仅发生在患者中,也发生在健康个体中。我们的数据显示,多巴胺与多巴胺 D1 受体的结合亲和力在左侧纹状体中明显高于右侧纹状体。对来自未处理、6-羟多巴胺损伤、左旋多巴处理和左旋多巴诱导的运动障碍大鼠的纹状体样本进行放射性配体结合分析的数据进行分析,显示出受体结构的差异,并提示了多巴胺与纹状体 D1 受体结合的右/左侧化的原因。此外,结合数据显示在左旋多巴(L-DOPA)诱导的运动障碍大鼠中,偏侧化丧失。