Cardiff School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, UK.
Eur J Neurosci. 2019 Feb;49(3):384-398. doi: 10.1111/ejn.14119. Epub 2018 Sep 16.
3,4-dihydroxy-L-phenylalanine (L-DOPA) is the gold standard treatment for Parkinson's disease. It has earned that title through its highly effective treatment of some of the motor symptoms in the early stages of the disease but it is a far from perfect drug. The inevitable long-term treatment that comes with this chronic neurodegenerative condition raises the risk significantly of the development of motor fluctuations including disabling L-DOPA-induced dyskinesia. Being unsurpassed as a therapy means that understanding the mechanisms of dyskinesia priming and induction is vital to the search for therapies to treat these side effects and allow optimal use of L-DOPA. However, L-DOPA use may also have consequences (positive or negative) for the development of other interventions, such as cell transplantation, which are designed to treat or repair the ailing brain. This review looks at the issues around the use of L-DOPA with a focus on its potential impact on advanced reparative interventions.
3,4-二羟基-L-苯丙氨酸(L-DOPA)是治疗帕金森病的金标准。它之所以获得这个称号,是因为它在疾病早期非常有效地治疗了一些运动症状,但它并不是一种完美的药物。这种慢性神经退行性疾病不可避免的长期治疗显著增加了运动波动的风险,包括使人丧失能力的 L-DOPA 诱导的运动障碍。作为一种治疗方法,无可比拟意味着理解运动障碍引发和诱导的机制对于寻找治疗这些副作用的疗法以及允许 L-DOPA 的最佳使用至关重要。然而,L-DOPA 的使用也可能对其他干预措施(如细胞移植)的发展产生影响(正面或负面),这些干预措施旨在治疗或修复患病的大脑。这篇综述着眼于 L-DOPA 的使用问题,重点关注其对先进修复干预措施的潜在影响。