Cognitive Aging Lab, Department of Psychology, Georgetown University Washington, DC, USA.
Department of Psychiatry, MedStar Georgetown University Hospital Washington, DC, USA.
Front Hum Neurosci. 2014 Aug 1;8:563. doi: 10.3389/fnhum.2014.00563. eCollection 2014.
Implicit sequence learning involves learning about dependencies in sequences of events without intent to learn or awareness of what has been learned. Sequence learning is related to striatal dopamine levels, striatal activation, and integrity of white matter connections. People with Parkinson's disease (PD) have degeneration of dopamine-producing neurons, leading to dopamine deficiency and therefore striatal deficits, and they have difficulties with sequencing, including complex language comprehension and postural stability. Most research on implicit sequence learning in PD has used motor-based tasks. However, because PD presents with motor deficits, it is difficult to assess whether learning itself is impaired in these tasks. The present study used an implicit sequence learning task with a reduced motor component, the Triplets Learning Task (TLT). People with PD and age- and education-matched healthy older adults completed three sessions (each consisting of 10 blocks of 50 trials) of the TLT. Results revealed that the PD group was able to learn the sequence, however, when learning was examined using a Half Blocks analysis (Nemeth et al., 2013), which compared learning in the 1st 25/50 trials of all blocks to that in the 2nd 25/50 trials, the PD group showed significantly less learning than Controls in the 2nd Half Blocks, but not in the 1st. Nemeth et al. (2013) hypothesized that the 1st Half Blocks involve recall and reactivation of the sequence learned, thus reflecting hippocampal-dependent learning, while the 2nd Half Blocks involve proceduralized behavior of learned sequences, reflecting striatal-based learning. The present results suggest that the PD group had intact hippocampal-dependent implicit sequence learning, but impaired striatal-dependent learning. Thus, sequencing deficits in PD are likely due to striatal impairments, but other brain systems, such as the hippocampus, may be able to partially compensate for striatal decline to improve performance.
内隐序列学习涉及到在事件序列中学习依赖关系,而没有学习或意识到已经学习了什么。序列学习与纹状体多巴胺水平、纹状体激活和白质连接的完整性有关。帕金森病(PD)患者的多巴胺产生神经元退化,导致多巴胺缺乏和纹状体缺陷,他们在序列方面存在困难,包括复杂语言理解和姿势稳定性。大多数 PD 患者的内隐序列学习研究都使用基于运动的任务。然而,由于 PD 存在运动缺陷,因此很难评估这些任务中的学习本身是否受到损害。本研究使用了一种运动成分较少的内隐序列学习任务,即三联体学习任务(TLT)。PD 患者和年龄及教育程度匹配的健康老年人完成了三次 TLT 会话(每次包括 10 个 50 次试验的块)。结果表明,PD 组能够学习序列,但当使用半块分析(Nemeth 等人,2013 年)检查学习时,即比较所有块的前 25/50 次试验的学习与后 25/50 次试验的学习,PD 组在后半块中的学习明显少于对照组,但在前半块中没有。Nemeth 等人(2013 年)假设前半块涉及已学习序列的回忆和再激活,因此反映了海马依赖的学习,而后半块涉及已学习序列的程序性行为,反映了基于纹状体的学习。本研究结果表明,PD 组具有完整的海马依赖内隐序列学习能力,但纹状体依赖学习受损。因此,PD 患者的序列缺陷可能是由于纹状体损伤引起的,但其他大脑系统,如海马体,可能能够部分补偿纹状体的下降,以提高表现。