Cellular bases for reward-related dopamine actions

被引:1
|
作者
Yagishita, Sho [1 ,2 ,3 ]
机构
[1] Univ Tokyo, Fac Med, Ctr Dis Biol & Integrat Med, Lab Struct Physiol, Bunkyo Ku, Tokyo, Japan
[2] Univ Tokyo, Int Res Ctr Neurointelligence WPI IRCN, UTIAS, Bunkyo Ku, Tokyo, Japan
[3] Univ Tokyo, Fac Med Expt Res, Ctr Dis Biol & Integrat Med, Fac Med,Lab Struct Physiol, Bldg N202, 7-3-1 Hongo, Bunkyo Ku, Tokyo 1130033, Japan
关键词
Dopamine; Dendritic spines; Structural plasticity; Reinforcement learning; Reward predication error; Eligibility trace; Dopamine D1 receptor; Dopamine D2 receptor; NUCLEUS-ACCUMBENS CORE; LONG-TERM POTENTIATION; STRUCTURAL PLASTICITY; INDIRECT PATHWAYS; STRIATAL NEURONS; ACTIVATION; RECEPTORS; PREDICTION; SYSTEM; NMDA;
D O I
10.1016/j.neures.2022.12.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dopamine neurons exhibit transient increases and decreases in their firing rate upon reward and punishment for learning. This bidirectional modulation of dopamine dynamics occurs on the order of hundreds of milliseconds, and it is sensitively detected to reinforce the preceding sensorimotor events. These observations indicate that the mechanisms of dopamine detection at the projection sites are of remarkable precision, both in time and con-centration. A major target of dopamine projection is the striatum, including the ventral region of the nucleus accumbens, which mainly comprises dopamine D1 and D2 receptor (D1R and D2R)-expressing spiny projection neurons. Although the involvement of D1R and D2R in dopamine-dependent learning has been suggested, the exact cellular bases for detecting transient dopamine signaling remain unclear. This review discusses recent cellular studies on the novel synaptic mechanisms for detecting dopamine transient signals associated with learning. Analyses of behavior based on these mechanisms have further revealed new behavioral aspects that are closely associated with these synaptic mechanisms. Thus, it is gradually possible to mechanistically explain behavioral learning via synaptic and cellular bases in rodents.
引用
收藏
页码:1 / 9
页数:9
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