Blaise J Harry
Department of Engineering and Neuroscience Program, Trinity College.
J Vis Exp. 2013 Nov 29(81):50642. doi: 10.3791/50642.
Studies of long-term potentiation of synaptic efficacy, an activity-dependent synaptic phenomenon having properties that make it attractive as a potential cellular mechanism underlying learning and information storage, have long been used to elucidate the physiology of various neuronal circuits in the hippocampus, amygdala, and other limbic and cortical structures. With this in mind, transgenic mouse models of neurological diseases represent useful platforms to conduct long-term potentiation (LTP) studies to develop a greater understanding of the role of genes in normal and abnormal synaptic communication in neuronal networks involved in learning, emotion and information processing. This article describes methodologies for reliably inducing LTP in the freely behaving mouse. These methodologies can be used in studies of transgenic and knockout freely behaving mouse models of neurodegenerative diseases.
突触效能的长期增强是一种依赖活动的突触现象,其特性使其作为学习和信息存储潜在细胞机制颇具吸引力。长期以来,此类研究一直用于阐明海马体、杏仁核以及其他边缘和皮质结构中各种神经回路的生理学。鉴于此,神经疾病的转基因小鼠模型是开展长期增强(LTP)研究的有用平台,有助于更深入了解基因在参与学习、情感和信息处理的神经网络中正常和异常突触通讯中的作用。本文介绍了在自由活动小鼠中可靠诱导LTP的方法。这些方法可用于神经退行性疾病转基因和基因敲除自由活动小鼠模型的研究。