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在 l-DOPA 诱导的运动模式选择中,神经元活动的压缩和截断的独特配置是基础。

Unique Configurations of Compression and Truncation of Neuronal Activity Underlie l-DOPA-Induced Selection of Motor Patterns in .

机构信息

Department of Neurobiology and Anatomy, W. M. Keck Center for the Neurobiology of Learning and Memory, McGovern Medical School at the University of Texas Health Science Center at Houston, Houston, TX 77030.

出版信息

eNeuro. 2017 Oct 24;4(5). doi: 10.1523/ENEURO.0206-17.2017. eCollection 2017 Sep-Oct.

Abstract

A key issue in neuroscience is understanding the ways in which neuromodulators such as dopamine modify neuronal activity to mediate selection of distinct motor patterns. We addressed this issue by applying either low or high concentrations of l-DOPA (40 or 250 μM) and then monitoring activity of up to 130 neurons simultaneously in the feeding circuitry of using a voltage-sensitive dye (RH-155). l-DOPA selected one of two distinct buccal motor patterns (BMPs): intermediate (low l-DOPA) or bite (high l-DOPA) patterns. The selection of intermediate BMPs was associated with shortening of the second phase of the BMP (retraction), whereas the selection of bite BMPs was associated with shortening of both phases of the BMP (protraction and retraction). Selection of intermediate BMPs was also associated with truncation of individual neuron spike activity (decreased burst duration but no change in spike frequency or burst latency) in neurons active during retraction. In contrast, selection of bite BMPs was associated with compression of spike activity (decreased burst latency and duration and increased spike frequency) in neurons projecting through specific nerves, as well as increased spike frequency of protraction neurons. Finally, large-scale voltage-sensitive dye recordings delineated the spatial distribution of neurons active during BMPs and the modification of that distribution by the two concentrations of l-DOPA.

摘要

神经科学中的一个关键问题是了解神经调质(如多巴胺)如何修饰神经元活动,从而介导不同运动模式的选择。我们通过应用低浓度或高浓度的 l-DOPA(40 或 250 μM),并使用电压敏感染料(RH-155)同时监测多达 130 个神经元的活动,来解决这个问题。l-DOPA 选择了两种不同的颊部运动模式(BMP)之一:中间(低 l-DOPA)或咬(高 l-DOPA)模式。中间 BMP 的选择与 BMP 第二阶段的缩短(回缩)有关,而咬 BMP 的选择与 BMP 两个阶段的缩短(伸出和回缩)有关。中间 BMP 的选择也与回缩期间活跃的单个神经元尖峰活动的截断(爆发持续时间缩短,但尖峰频率或爆发潜伏期没有变化)有关。相比之下,咬 BMP 的选择与通过特定神经投射的神经元的尖峰活动的压缩(爆发潜伏期和持续时间缩短,尖峰频率增加)有关,以及伸出神经元的尖峰频率增加有关。最后,大规模电压敏感染料记录描绘了 BMP 期间活跃的神经元的空间分布,以及两种浓度的 l-DOPA 对该分布的修饰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2816/5654236/eb6757ae8b5e/enu005172435r001.jpg

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