裸子电感觉叶的慢通路:场电位和单一活动

Ana Carolina Pereira, Alejo Rodríguez-Cattáneo, Angel A. Caputi
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引用次数: 14

摘要

本文首次报道了脉冲弱电鱼裸鱼电感觉叶的自激活模式。沿着垂直轨迹(50 μm步长)和横跨电感觉叶的横向晶格阵列(分辨率50 μm × 100 μm)记录响应鱼自身电器官放电(EOD)的场电位。在同一实验中记录了82个神经元的单一活动。场电位分析表明,缓慢的电感觉路径显示出一种典型的eod后活动模式,其特征包括三个主要事件:(i)约7 ms时的小而早期分量,(ii)约13 ms时的中间峰,(iii) 20 ms后的晚宽分量峰。单位放电速率显示了3到30毫秒之间的广泛延迟和不同数量的尖峰(中位数为0.28个单位/EOD)。条件概率分析显示单模态和多模态排爆后直方图,单位活动直方图的峰值通常与场电位主要成分的时间相匹配。单峰响应被分类为锁相单峰(方差小于1 ms)、早期单峰(中间方差,通常以双峰形式发射,峰值范围为10 - 17 ms)和晚期单峰(大方差,通常发射间隔约10 ms的两个尖峰,峰值超过17 ms)。多模态单位的反应表明,在排爆后,它们的射击概率要么增加,要么降低。在最后一种(压抑的)单元亚型中,概率在EOD之后下降。早期抑制和早期锁相单元的存在表明,观察到的模式可能受到快速前馈抑制的影响。我们得出结论,脉冲裸子形中的ELL在一系列复杂的事件中被激活,这些事件反映了ELL网络的连通性。
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The slow pathway in the electrosensory lobe of Gymnotus omarorum: Field potentials and unitary activity

This is a first communication on the self-activation pattern of the electrosensory lobe in the pulse weakly electric fish Gymnotus omarorum. Field potentials in response to the fish’s own electric organ discharge (EOD) were recorded along vertical tracks (50 μm step) and on a transversal lattice array across the electrosensory lobe (resolution 50 μm × 100 μm). The unitary activity of 82 neurons was recorded in the same experiments. Field potential analysis indicates that the slow electrosensory path shows a characteristic post-EOD pattern of activity marked by three main events: (i) a small and early component at about 7 ms, (ii) an intermediate peak about 13 ms and (iii) a late broad component peaking after 20 ms. Unit firing rate showed a wide range of latencies between 3 and 30 ms and a variable number of spikes (median 0.28 units/EOD). Conditional probability analysis showed monomodal and multimodal post-EOD histograms, with the peaks of unit activity histograms often matching the timing of the main components of the field potentials. Monomodal responses were sub-classified as phase locked monomodal (variance smaller than 1 ms), early monomodal (intermediate variance, often firing in doublets, peaking range 10–17 ms) and late monomodal (large variance, often firing two spikes separated about 10 ms, peaking beyond 17 ms). The responses of multimodal units showed that their firing probability was either enhanced, or depressed just after the EOD. In this last (depressed) subtype of unit the probability stepped down just after the EOD. Early inhibition and the presence of early phase locked units suggest that the observed pattern may be influenced by a fast feed forward inhibition. We conclude that the ELL in pulse gymnotiformes is activated in a complex sequence of events that reflects the ELL network connectivity.

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来源期刊
Journal of Physiology-Paris
Journal of Physiology-Paris 医学-神经科学
CiteScore
2.02
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Each issue of the Journal of Physiology (Paris) is specially commissioned, and provides an overview of one important area of neuroscience, delivering review and research papers from leading researchers in that field. The content will interest both those specializing in the experimental study of the brain and those working in interdisciplinary fields linking theory and biological data, including cellular neuroscience, mathematical analysis of brain function, computational neuroscience, biophysics of brain imaging and cognitive psychology.
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