Brain Mechanisms for Behaviour Unit, Okinawa Institute of Science and Technology, Okinawa, Japan.
Parkinsonism Relat Disord. 2009 Dec;15 Suppl 3:S139-42. doi: 10.1016/S1353-8020(09)70801-6.
Any simplified description of a brain system that survives 20 years is bound to have some problems. Twenty years of research should have added details that were not known when the now classical description of the basal ganglia circuitry was new. Some examples of such new information about the parts of the original model include: All of these details make it difficult to cling to the model as it was presented, but which of the new information will support a new synthesis? Do we have a coherent replacement for those powerfully heuristic ideas put forward by Albin Young and Penny in 1989? Perhaps in the quantitative anatomical detail there is a plan that may support a new theory. If all of the cortex is not accessible to every striatal cell. If dopamine influences many spines rather than the one it contacts. If we stop looking for a mechanical control system for movement in the basal ganglia and begin to investigate the predictive properties of 'reinforcement learning'. Then maybe a new functional model will emerge that is less tied to anatomical and physiological simplification, but perhaps will still allow us to engineer therapeutic strategies to help patients with movement disorders.
任何对存活 20 年的大脑系统的简化描述都必然存在一些问题。在现在经典的基底神经节回路描述出现 20 年后,应该已经增加了一些当时未知的细节。关于原始模型的部分,这些新信息的一些例子包括:所有这些细节都使得难以坚持原始模型,但哪些新信息将支持新的综合呢?我们是否有一个连贯的替代方案来替代 Albin Young 和 Penny 在 1989 年提出的那些强有力的启发式想法?也许在定量解剖细节中,有一个计划可能支持一个新的理论。如果并非每一个纹状体细胞都能与所有的皮层连接。如果多巴胺影响许多而不仅仅是它接触的一个棘突。如果我们不再寻找基底神经节中运动的机械控制系统,而是开始研究“强化学习”的预测特性。那么,也许一个新的功能模型将出现,它与解剖和生理学简化的联系较少,但也许仍然允许我们设计治疗策略来帮助运动障碍患者。