Getting Excited About Learning.
Getting Excited About Learning.
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对学习感到兴奋。
DOI:
10.1093/function/zqab059
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发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Matikainen-Ankney,Bridget
中科院分区:
文献类型:
--
作者:
Matikainen-Ankney,Bridget
Motor learning is thought to involve an increase in the synaptic strength of glutamatergic inputs to the dorsolateral striatum (DLS), enhancing striatal activity and invigorating specific actions. 1 However, the cell types that govern this change in synaptic strength remain unknown. The striatum comprises two principal cell types, known as direct and indirect pathway neurons (dSPNs and iSPNs), as well as multiple classes of interneurons. A “classic” model of basal ganglia function predicts that dSPNs and iSPNs oppose one another during action generation, with dSPNs invigorating actions and iSPNs opposing competing or interfering actions. 2 However, more recent models of basal ganglia function have noted that both dSPNs and iSPNs are activated during actions and action preparation, 3 leading to proposals that these cell types work together in a complementary or competitive manner to govern movement. 4 Here, with an impressive set of electrophysiological recordings in awake mice, Sippy et al. further our understanding of these models, and of how synaptic inputs onto specific striatal cell types change following motor learning.Previously in 2015, Sippy et al. 5 used whole cell in vivo recordings to monitor membrane voltages of individual DLS neurons in a sensorimotor-association task. The authors used a magnetic coil and a small metal bead to deflect a single whisker of the mice, which signaled the availability of water. They tested this in trained mice that had learned to associate the whisker deflection with the availability of water and started licking shortly after this deflection. They found that both dSPNs and iSPNs were depolarized in response to this whisker stimulation, with dSPNs exhibiting a more rapid depolarization than iSPNs. This approach provided direct electrophysiological evidence linking this learned motor action to excitatory synaptic input to the DLS and increased our understanding of how synaptic inputs drive