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Aging impairs intermediate-term behavioral memory by disrupting the dorsal paired medial neuron memory trace

机译:衰老通过破坏背对内侧神经元记忆轨迹而损害中期行为记忆

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摘要

How the functional activity of the brain is altered during aging to cause age-related memory impairments is unknown. We used functional cellular imaging to monitor two different calcium-based memory traces that underlie olfactory classical conditioning in young and aged Drosophila. Functional imaging of neural activity in the processes of the dorsal paired medial (DPM) and mushroom body neurons revealed that the capacity to form an intermediate-term memory (ITM) trace in the DPM neurons after learning is lost with age, whereas the capacity to form a short-term memory trace in the α'/β' mushroom body neurons remains unaffected by age. Stimulation of the DPM neurons by activation of a temperature-sensitive cation channel between acquisition and retrieval enhanced ITM in aged but not young flies. These data indicate that the functional state of the DPM neurons is selectively altered with age to cause an age-related impairment of ITM, and demonstrate that altering the excitability of DPM neurons can restore age-related memory impairments.
机译:在衰老过程中如何改变大脑的功能活动以引起与年龄相关的记忆障碍。我们使用功能性细胞成像来监测两个不同的基于钙的记忆痕迹,这些痕迹是年轻和老年果蝇嗅觉经典条件的基础。背对内侧(DPM)和蘑菇体神经元过程中神经活动的功能成像显示,学习后DPM神经元中形成中期记忆(ITM)轨迹的能力随年龄而丧失,而在蘑菇体神经元中形成的短期记忆痕迹不受年龄的影响。通过激活获取和获取之间的温度敏感阳离子通道来刺激DPM神经元,可增强老年但非幼蝇的ITM。这些数据表明,DPM神经元的功能状态随年龄而选择性地改变,从而引起与年龄有关的ITM损伤,并表明改变DPM神经元的兴奋性可以恢复与年龄有关的记忆障碍。

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