Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
Trends Neurosci. 2013 Sep;36(9):543-54. doi: 10.1016/j.tins.2013.06.003. Epub 2013 Jul 19.
For several decades, the dopamine precursor levodopa has been the primary therapy for Parkinson's disease (PD). However, not all of the motor and non-motor features of PD can be attributed solely to dopaminergic dysfunction. Recent clinical and preclinical advances provide a basis for the identification of additional innovative therapeutic options to improve the management of the disease. Novel pharmacological strategies must be optimized for PD by: (i) targeting disturbances of the serotonergic, noradrenergic, glutamatergic, GABAergic, and cholinergic systems in addition to the dopaminergic system, and (ii) characterizing alterations in the levels of neurotransmitter receptors and transporters that are associated with the various manifestations of the disease.
几十年来,多巴胺前体左旋多巴一直是治疗帕金森病(PD)的主要方法。然而,并非 PD 的所有运动和非运动特征都可以仅仅归因于多巴胺能功能障碍。最近的临床和临床前进展为确定其他创新治疗选择提供了基础,以改善疾病的管理。新型药理学策略必须通过以下方式针对 PD 进行优化:(i)除了多巴胺系统之外,还针对 5-羟色胺能、去甲肾上腺素能、谷氨酸能、γ-氨基丁酸能和胆碱能系统的紊乱进行靶向治疗,以及(ii)描述与疾病各种表现相关的神经递质受体和转运体水平的改变。