Véronneau-Veilleux Florence, Ursino Mauro, Robaey Philippe, Lévesque Daniel, Nekka Fahima
Faculté de Pharmacie, Université de Montréal, Montréal, Québec H3C 3J7, Canada.
Department of Electrical, Electronic and Information Engineering "Guglielmo Marconi," University of Bologna, 40136 Bologna, Italy.
Chaos. 2020 Sep;30(9):093146. doi: 10.1063/5.0014800.
The effect of levodopa in alleviating the symptoms of Parkinson's disease is altered in a highly nonlinear manner as the disease progresses. This can be attributed to different compensation mechanisms taking place in the basal ganglia where the dopaminergic neurons are progressively lost. This alteration in the effect of levodopa complicates the optimization of a drug regimen. The present work aims at investigating the nonlinear dynamics of Parkinson's disease and its therapy through mechanistic mathematical modeling. Using a holistic approach, a pharmacokinetic model of levodopa was combined to a dopamine dynamics and a neurocomputational model of basal ganglia. The influence of neuronal death on these different mechanisms was also integrated. Using this model, we were able to investigate the nonlinear relationships between the levodopa plasma concentration, the dopamine brain concentration, and a response to a motor task. Variations in dopamine concentrations in the brain for different levodopa doses were also studied. Finally, we investigated the narrowing of a levodopa therapeutic index with the progression of the disease as a result of these nonlinearities. In conclusion, various consequences of nonlinear dynamics in Parkinson's disease treatment were studied by developing an integrative model. This model paves the way toward individualization of a dosing regimen. Using sensor based information, the parameters of the model could be fitted to individual data to propose optimal individual regimens.
随着帕金森病的进展,左旋多巴缓解帕金森病症状的效果会以高度非线性的方式发生改变。这可归因于基底神经节中发生的不同代偿机制,在基底神经节中多巴胺能神经元会逐渐丧失。左旋多巴效果的这种改变使药物治疗方案的优化变得复杂。目前的工作旨在通过机理数学建模研究帕金森病及其治疗的非线性动力学。采用整体方法,将左旋多巴的药代动力学模型与多巴胺动力学以及基底神经节的神经计算模型相结合。还整合了神经元死亡对这些不同机制的影响。利用该模型,我们能够研究左旋多巴血浆浓度、多巴胺脑浓度与运动任务反应之间的非线性关系。还研究了不同左旋多巴剂量下脑内多巴胺浓度的变化。最后,我们研究了由于这些非线性因素导致的随着疾病进展左旋多巴治疗指数的变窄。总之,通过建立一个综合模型研究了帕金森病治疗中非线性动力学的各种后果。该模型为给药方案的个体化铺平了道路。利用基于传感器的信息,可将模型参数拟合到个体数据以提出最佳个体化方案。