Al-Onaizi Mohammed A, Parfitt Gustavo M, Kolisnyk Benjamin, Law Clayton S H, Guzman Monica S, Barros Daniela Martí, Leung L Stan, Prado Marco A M, Prado Vania F
Robarts Research Institute.
Department of Anatomy and Cell Biology.
Cereb Cortex. 2017 Feb 1;27(2):1615-1628. doi: 10.1093/cercor/bhv349.
Cholinergic dysfunction has been associated with cognitive abnormalities in a variety of neurodegenerative and neuropsychiatric diseases. Here we tested how information processing is regulated by cholinergic tone in genetically modified mice targeting the vesicular acetylcholine transporter (VAChT), a protein required for acetylcholine release. We measured long-term potentiation of Schaffer collateral-CA1 synapses in vivo and assessed information processing by using a mouse touchscreen version of paired associates learning task (PAL). Acquisition of information in the mouse PAL task correlated to levels of hippocampal VAChT, suggesting a critical role for cholinergic tone. Accordingly, synaptic plasticity in the hippocampus in vivo was disturbed, but not completely abolished, by decreased hippocampal cholinergic signaling. Disrupted forebrain cholinergic signaling also affected working memory, a result reproduced by selectively decreasing VAChT in the hippocampus. In contrast, spatial memory was relatively preserved, whereas reversal spatial memory was sensitive to decreased hippocampal cholinergic signaling. This work provides a refined roadmap of how synaptically secreted acetylcholine influences distinct behaviors and suggests that distinct forms of cognitive processing may be regulated in different ways by cholinergic activity.
胆碱能功能障碍与多种神经退行性疾病和神经精神疾病中的认知异常有关。在此,我们测试了在靶向囊泡乙酰胆碱转运体(VAChT,一种乙酰胆碱释放所需的蛋白质)的转基因小鼠中,胆碱能张力如何调节信息处理。我们在体内测量了海马体中谢弗侧支- CA1突触的长时程增强,并通过使用配对联想学习任务(PAL)的小鼠触摸屏版本评估信息处理。小鼠PAL任务中的信息获取与海马体VAChT水平相关,表明胆碱能张力起着关键作用。相应地,海马体胆碱能信号减少会扰乱但不会完全消除体内海马体的突触可塑性。前脑胆碱能信号中断也会影响工作记忆,这一结果在选择性降低海马体中VAChT时得以重现。相比之下,空间记忆相对保留,而空间记忆反转对海马体胆碱能信号减少敏感。这项工作为突触分泌的乙酰胆碱如何影响不同行为提供了一份详细的路线图,并表明不同形式的认知处理可能受到胆碱能活动的不同调节。