Start/stop signals emerge in nigrostriatal circuits during sequence learning

被引:411
作者
Jin, Xin [1 ]
Costa, Rui M. [1 ,2 ]
机构
[1] NIAAA, Lab Integrat Neurosci, NIH, Bethesda, MD 20892 USA
[2] Inst Gulbenkian Ciencias, Champalimaud Neurosci Programme, P-2780156 Oeiras, Portugal
基金
欧洲研究理事会;
关键词
DOPAMINE NEURONS ENCODE; HUNTINGTONS-DISEASE; BASAL GANGLIA; STRIATUM; REPRESENTATION; PATTERN; TIME; POPULATIONS; INITIATION; MOVEMENTS;
D O I
10.1038/nature09263
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Learning new action sequences subserves a plethora of different abilities such as escaping a predator, playing the piano, or producing fluent speech. Proper initiation and termination of each action sequence is critical for the organization of behaviour, and is compromised in nigrostriatal disorders like Parkinson's and Huntington's diseases. Using a self-paced operant task in which mice learn to perform a particular sequence of actions to obtain an outcome, we found neural activity in nigrostriatal circuits specifically signalling the initiation or the termination of each action sequence. This start/stop activity emerged during sequence learning, was specific for particular actions, and did not reflect interval timing, movement speed or action value. Furthermore, genetically altering the function of striatal circuits disrupted the development of start/stop activity and selectively impaired sequence learning. These results have important implications for understanding the functional organization of actions and the sequence initiation and termination impairments observed in basal ganglia disorders.
引用
收藏
页码:457 / 462
页数:6
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