Department of Biomedical Sciences, Section of Physiology, University of Cagliari, Cittadella Universitaria, SS554, Km 4.5, 09042, Monserrato, Italy.
Division of Neurobiology, Department of Experimental Medical Science, Wallenberg Neuroscience Center, Lund University, 221 84, Lund, Sweden.
J Neural Transm (Vienna). 2018 Aug;125(8):1195-1202. doi: 10.1007/s00702-018-1865-5. Epub 2018 Feb 26.
During the last decade, the serotonergic system has emerged as a key player in the appearance of L-DOPA-induced dyskinesia in animal models of Parkinson's disease. Clinical investigations, based on imaging and postmortem analyses, suggest that the serotonin neurons are also involved in the etiology of this complication of long-term L-DOPA treatment in parkinsonian patients. These findings have stimulated efforts to develop new therapies using drugs targeting the malfunctioning serotonin neurons. In this review, we summarize the experimental and clinical data obtained so far and discuss the prospects for further development of this therapeutic strategy.
在过去的十年中,5-羟色胺能系统已成为帕金森病动物模型中出现左旋多巴诱导运动障碍的关键因素。基于影像学和尸检分析的临床研究表明,5-羟色胺能神经元也参与了帕金森病患者长期接受左旋多巴治疗后出现这种并发症的病因。这些发现促使人们努力开发使用针对功能失调的 5-羟色胺能神经元的药物的新疗法。在这篇综述中,我们总结了迄今为止获得的实验和临床数据,并讨论了进一步发展这种治疗策略的前景。