Paula T Kuokkanen, Ira Kraemer, Christine Koeppl, Catherine E Carr, Richard Kempter
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We simultaneously recorded NM neurons' spikes and the EEG, and found that ≥ 5, 000 spontaneous single-cell spikes are necessary to isolate a significant spike-triggered average response at the EEG electrode. An average single-neuron contribution to the ABR was predicted by convolving the spike-triggered average with the cell's peri-stimulus time histogram. Amplitudes of predicted contributions of single NM cells typically reached 32.9 ± 1.1 nV (mean ± SE, range: 2.5 - 162.7 nV), or 0.07 ± 0.02% (median ± SE; range from 0.01% to 1%) of the ABR amplitude. The time of the predicted peak coincided best with the peak of the ABR wave II, independent of the click sound level. Our results suggest that individual neurons' contributions to an EEG can vary widely, and that wave II of the ABR is shaped by NM units.</p><p><strong>Significance statement: </strong>The auditory brainstem response (ABR) is a scalp potential used for the diagnosis of hearing loss, both clinically and in research. 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引用次数: 0
摘要
听性脑干反应(ABR)是一种声诱发脑电图电位,是诊断听力损失(尤其是新生儿听力损失)的重要工具。ABR 起源于听性脑干核的反应序列,点击诱发的 ABR 通常会在前 6 毫秒内出现三个正峰值("波")。然而,很难将 ABR 波归属于特定来源,也无法量化 ABR 波的贡献。在这里,我们利用仓鸮一阶耳蜗大细胞核(NM)的大尺寸和物理分离来估计单细胞对 ABR 的贡献。我们同时记录了 NM 神经元的尖峰和脑电图,发现要在脑电图电极上分离出显著的尖峰触发平均响应,需要 5,000 个自发单细胞尖峰。通过将尖峰触发的平均值与细胞的刺激周围时间直方图进行卷积,可以预测单神经元对 ABR 的平均贡献。单个 NM 细胞的预测贡献振幅通常达到 32.9 ± 1.1 nV(平均值 ± SE,范围:2.5 - 162.7 nV),或 ABR 振幅的 0.07 ± 0.02%(中位数 ± SE,范围:0.01 - 4.0%)。预测峰值的时间与 ABR 波 II 的峰值最为吻合,这种吻合与点击音量无关。我们的研究结果表明,ABR 波 II 是由一小部分 NM 单元形成的:听性脑干反应(ABR)是一种头皮电位,用于临床和研究中听力损失的诊断。我们研究了来自听性脑干神经元的单个动作电位对 ABR 的贡献,并提供了直接证据,证明在一阶听觉神经核中记录的动作电位及其脑电图贡献与 ABR 波 II 相吻合。研究还表明,单个细胞对整个群体的贡献存在很大差异。
Single neuron contributions to the auditory brainstem EEG.
The auditory brainstem response (ABR) is an acoustically evoked EEG potential that is an important diagnostic tool for hearing loss, especially in newborns. The ABR originates from the response sequence of auditory nerve and brainstem nuclei, and a click-evoked ABR typically shows three positive peaks ('waves') within the first six milliseconds. However, an assignment of the waves of the ABR to specific sources is difficult, and a quantification of contributions to the ABR waves is not available. Here, we exploit the large size and physical separation of the barn owl first-order cochlear nucleus magnocellularis (NM) to estimate single-cell contributions to the ABR. We simultaneously recorded NM neurons' spikes and the EEG, and found that ≥ 5, 000 spontaneous single-cell spikes are necessary to isolate a significant spike-triggered average response at the EEG electrode. An average single-neuron contribution to the ABR was predicted by convolving the spike-triggered average with the cell's peri-stimulus time histogram. Amplitudes of predicted contributions of single NM cells typically reached 32.9 ± 1.1 nV (mean ± SE, range: 2.5 - 162.7 nV), or 0.07 ± 0.02% (median ± SE; range from 0.01% to 1%) of the ABR amplitude. The time of the predicted peak coincided best with the peak of the ABR wave II, independent of the click sound level. Our results suggest that individual neurons' contributions to an EEG can vary widely, and that wave II of the ABR is shaped by NM units.
Significance statement: The auditory brainstem response (ABR) is a scalp potential used for the diagnosis of hearing loss, both clinically and in research. We investigated the contribution of single action potentials from auditory brainstem neurons to the ABR and provide direct evidence that action potentials recorded in a first order auditory nucleus, and their EEG contribution, coincide with wave II of the ABR. The study also shows that the contribution of single cells varies strongly across the population.