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多巴胺作用于树突棘结构可塑性的关键时间窗口。

A critical time window for dopamine actions on the structural plasticity of dendritic spines.

机构信息

Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan. Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan. Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan. Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

出版信息

Science. 2014 Sep 26;345(6204):1616-20. doi: 10.1126/science.1255514.

Abstract

Animal behaviors are reinforced by subsequent rewards following within a narrow time window. Such reward signals are primarily coded by dopamine, which modulates the synaptic connections of medium spiny neurons in the striatum. The mechanisms of the narrow timing detection, however, remain unknown. Here, we optically stimulated dopaminergic and glutamatergic inputs separately and found that dopamine promoted spine enlargement only during a narrow time window (0.3 to 2 seconds) after the glutamatergic inputs. The temporal contingency was detected by rapid regulation of adenosine 3',5'-cyclic monophosphate in thin distal dendrites, in which protein-kinase A was activated only within the time window because of a high phosphodiesterase activity. Thus, we describe a molecular basis of reinforcement plasticity at the level of single dendritic spines.

摘要

动物行为会在狭窄的时间窗口内受到后续奖励的强化。这种奖励信号主要由多巴胺编码,多巴胺调节纹状体中中间神经元的突触连接。然而,狭窄时间检测的机制仍然未知。在这里,我们分别用光刺激多巴胺能和谷氨酸能输入,发现多巴胺仅在谷氨酸能输入后 0.3 到 2 秒的狭窄时间窗口内促进脊柱扩张。时间关联是通过薄的远端树突中快速调节环磷酸腺苷来检测的,其中蛋白激酶 A 仅在时间窗口内被激活,因为磷酸二酯酶活性很高。因此,我们描述了在单个树突棘水平上强化可塑性的分子基础。

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