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作为大脑的功能状态的学习:野生型和转基因动物的研究。

Learning as a Functional State of the Brain: Studies in Wild-Type and Transgenic Animals.

机构信息

Division of Neurosciences, Pablo de Olavide University, Ctra. de Utrera, Km. 1, Seville, 41013, Spain.

出版信息

Adv Exp Med Biol. 2017;1015:75-93. doi: 10.1007/978-3-319-62817-2_5.

Abstract

Contemporary neuroscientists are paying increasing attention to subcellular, molecular, and electrophysiological mechanisms underlying learning and memory processes. Recent studies have examined the development of transgenic mice affected at different stages of the learning process, or have emulated in animals various human pathological conditions involving cognition and motor learning. However, a parallel effort is needed to develop stimulating and recording techniques suitable for use in behaving mice in order to understand activity-dependent synaptic changes taking place during the very moment of the learning process. The in vivo models should incorporate information collected from different molecular and in vitro approaches. Long-term potentiation (LTP) has been proposed as the neural mechanism underlying synaptic plasticity, and NMDA receptors have been proposed as the molecular substrate of LTP. It now seems necessary to study the relationship of both LTP and NMDA receptors to functional changes in synaptic efficiency taking place during actual learning in selected cerebral cortical structures. Here, we review data collected in our laboratory during the past 10 years on the involvement of different hippocampal synapses in the acquisition of the classically conditioned eyelid responses in behaving mice. Overall the results indicate a specific contribution of each cortical synapse to the acquisition and storage of new motor and cognitive abilities. Available data show that LTP, evoked by high-frequency stimulation of Schaffer collaterals, disturbs both the acquisition of conditioned eyelid responses and the physiological changes that occur at hippocampal synapses during learning. Moreover, the administration of NMDA-receptor antagonists is able not only to prevent LTP induction in vivo, but also to hinder both the formation of conditioned eyelid responses and functional changes in the strength of the CA3-CA1 synapse. Nevertheless, many other neurotransmitter receptors, intracellular mediators, and transcription factors are also involved in learning and memory processes. In summary, it can be proposed that learning and memory in behaving mammals are the result of the activation of complex and distributed functional states involving many different cerebral cortical synapses, with the participation also of various neurotransmitter systems.

摘要

当代神经科学家越来越关注学习和记忆过程的亚细胞、分子和电生理机制。最近的研究检查了受学习过程不同阶段影响的转基因小鼠的发展,或者在动物身上模拟了各种涉及认知和运动学习的人类病理状况。然而,需要平行努力开发适合在行为小鼠中使用的刺激和记录技术,以便了解学习过程中发生的依赖活动的突触变化。体内模型应纳入从不同分子和体外方法收集的信息。长时程增强(LTP)被提议作为突触可塑性的神经机制,而 NMDA 受体被提议作为 LTP 的分子基础。现在似乎有必要研究 LTP 和 NMDA 受体与在选定的大脑皮质结构中实际学习期间发生的突触效率的功能变化之间的关系。在这里,我们回顾了我们实验室在过去 10 年中收集的有关不同海马突触参与行为小鼠经典条件反射眨眼反应获得的数据。总体而言,结果表明每个皮质突触都对新的运动和认知能力的获得和存储有特定的贡献。现有数据表明,高频刺激 Schaffer 侧支引起的 LTP 不仅干扰了条件反射眨眼反应的获得,也干扰了学习过程中海马突触发生的生理变化。此外,NMDA 受体拮抗剂的给药不仅能够防止体内 LTP 的诱导,而且能够阻止条件反射眨眼反应的形成和 CA3-CA1 突触强度的功能变化。然而,许多其他神经递质受体、细胞内介质和转录因子也参与学习和记忆过程。总之,可以提出,行为哺乳动物的学习和记忆是涉及许多不同大脑皮质突触的复杂和分布式功能状态的激活的结果,还涉及各种神经递质系统的参与。

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