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OSCILLATORY POTENTIALS OF THE SLOW-SEQUENCE MULTIFOCAL ERG IN PRIMATES EXTRACTED USING THE MATCHING PURSUIT METHOD

机译:匹配追踪法提取的慢速多焦点ERG在本底中的振荡势

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摘要

This study used the Matching Pursuit (MP) method, a time-frequency analysis, to identify and characterize oscillatory potentials (OPs) in the primate electroretinogram (ERG). When the slow-sequence mfERG from the macular region of the retina was matched with Gabor functions, OPs were identified in two distinct bands: a high-frequency band peaking around 150 Hz that contributes to early OPs, and a low-frequency band peaking around 80 Hz that contributes to both early and late OPs. Pharmacological blockade and experimental glaucoma studies showed that the high-frequency OPs depend upon sodium-dependent spiking activity of retinal ganglion cells, whereas the low-frequency OPs depend primarily upon non-spiking activity of amacrine cells, and more distal retinal activity.
机译:这项研究使用了匹配追踪(MP)方法(一种时频分析)来识别和表征灵长类视网膜电图(ERG)中的振荡电位(OPs)。当来自视网膜黄斑区的慢序列mfERG与Gabor功能相匹配时,在两个不同的频带中识别出OP:在150 Hz左右峰值的高频带有助于早期OP,在低频附近出现峰值的低频频带。 80 Hz有助于早期和晚期OP。药理学阻滞和实验性青光眼研究表明,高频OP依赖于视网膜神经节细胞的钠依赖性加标活性,而低频OP则主要依赖于无长突细胞的非加标活性以及更多的远端视网膜活性。

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