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

机译:多巴胺作用对树突棘结构可塑性的关键时间窗

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摘要

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.
机译:在狭窄的时间范围内,随后的奖励会增强动物的行为。这种奖励信号主要由多巴胺编码,多巴胺可调节纹状体中棘状神经元的突触连接。但是,窄定时检测的机制仍然未知。在这里,我们分别对多巴胺能和谷氨酸能的输入进行光学刺激,发现多巴胺仅在谷氨酸能输入后的狭窄时间窗口(0.3至2秒)内促进脊柱增大。通过快速调节远端远端树突状腺苷3',5'-环一磷酸来检测时间偶然性,其中由于高的磷酸二酯酶活性,蛋白激酶A仅在时间窗口内被激活。因此,我们描述了单个树突棘水平的增强可塑性的分子基础。

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