Niccolini F, Loane C, Politis M
Department of Medicine, Hammersmith Hospital, Imperial College London, London, UK; Neurodegeneration Imaging Group, Department of Clinical Neuroscience, King's College London, London, UK.
Eur J Neurol. 2014 May;21(5):694-9, e39-43. doi: 10.1111/ene.12362. Epub 2014 Jan 28.
Levodopa-induced dyskinesias (LIDs) and graft-induced dyskinesias (GIDs) are serious and common complications of Parkinson's disease (PD) management following chronic treatment with levodopa or intrastriatal transplantation with dopamine-rich foetal ventral mesencephalic tissue, respectively. Positron emission tomography (PET) molecular imaging provides a powerful in vivo tool that has been employed over the past 20 years for the elucidation of mechanisms underlying the development of LIDs and GIDs in PD patients. PET used together with radioligands tagging molecular targets has allowed the functional investigation of several systems in the brain including the dopaminergic, serotonergic, glutamatergic, opioid, endocannabinoid, noradrenergic and cholinergic systems. In this article the role of PET imaging in unveiling pathophysiological mechanisms underlying the development of LIDs and GIDs in PD patients is reviewed.
左旋多巴诱发的异动症(LIDs)和移植诱发的异动症(GIDs)分别是帕金森病(PD)患者长期接受左旋多巴治疗或纹状体内移植富含多巴胺的胎儿腹侧中脑组织后出现的严重且常见的并发症。正电子发射断层扫描(PET)分子成像提供了一种强大的体内工具,在过去20年中一直用于阐明PD患者中LIDs和GIDs发生的潜在机制。PET与标记分子靶点的放射性配体一起使用,使得对大脑中包括多巴胺能、5-羟色胺能、谷氨酸能、阿片样物质、内源性大麻素、去甲肾上腺素能和胆碱能系统在内的多个系统进行功能研究成为可能。本文综述了PET成像在揭示PD患者中LIDs和GIDs发生的病理生理机制方面的作用。