Department of Psychology, Neuroscience & Behaviour, McMaster University Hamilton, ON, Canada.
Front Neural Circuits. 2012 Aug 20;6:56. doi: 10.3389/fncir.2012.00056. eCollection 2012.
Neural responses in the mammalian auditory midbrain (inferior colliculus; IC) arise from complex interactions of synaptic excitation, inhibition, and intrinsic properties of the cell. Temporally selective duration-tuned neurons (DTNs) in the IC are hypothesized to arise through the convergence of excitatory and inhibitory synaptic inputs offset in time. Synaptic inhibition can be inferred from extracellular recordings by presenting pairs of pulses (paired tone stimulation) and comparing the evoked responses of the cell to each pulse. We obtained single unit recordings from the IC of the awake big brown bat (Eptesicus fuscus) and used paired tone stimulation to measure the recovery cycle times of DTNs and non-temporally selective auditory neurons. By systematically varying the interpulse interval (IPI) of the paired tone stimulus, we determined the minimum IPI required for a neuron's spike count or its spike latency (first- or last-spike latency) in response to the second tone to recover to within ≥50% of the cell's baseline count or to within 1 SD of it's baseline latency in response to the first tone. Recovery times of shortpass DTNs were significantly shorter than those of bandpass DTNs, and recovery times of bandpass DTNs were longer than allpass neurons not selective for stimulus duration. Recovery times measured with spike counts were positively correlated with those measured with spike latencies. Recovery times were also correlated with first-spike latency (FSL). These findings, combined with previous studies on duration tuning in the IC, suggest that persistent inhibition is a defining characteristic of DTNs. Herein, we discuss measuring recovery times of neurons with spike counts and latencies. We also highlight how persistent inhibition could determine neural recovery times and serve as a potential mechanism underlying the precedence effect in humans. Finally, we explore implications of recovery times for DTNs in the context of bat hearing and echolocation.
哺乳动物听觉中脑(下丘;IC)中的神经反应源自突触兴奋、抑制和细胞固有特性的复杂相互作用。IC 中具有时间选择性的持续时间调谐神经元(DTN)被假设通过时间偏移的兴奋性和抑制性突触输入的会聚而产生。通过呈现一对脉冲(成对音调刺激)并比较细胞对每个脉冲的诱发反应,可以从细胞外记录中推断出突触抑制作用。我们从清醒的大棕蝠(Eptesicus fuscus)的 IC 中获得了单细胞记录,并使用成对音调刺激来测量 DTN 和非时间选择性听觉神经元的恢复循环时间。通过系统地改变成对音调刺激的脉冲间隔(IPI),我们确定了神经元的尖峰计数或其尖峰潜伏期(第一或最后尖峰潜伏期)对第二个音调的响应恢复到细胞基线计数的≥50%或对第一个音调的响应恢复到其基线潜伏期的 1 SD 所需的最小 IPI。短通 DTN 的恢复时间明显短于带通 DTN 的恢复时间,而带通 DTN 的恢复时间长于对刺激持续时间没有选择性的全通神经元。用尖峰计数测量的恢复时间与用尖峰潜伏期测量的恢复时间呈正相关。恢复时间也与第一尖峰潜伏期(FSL)相关。这些发现与 IC 中持续时间调谐的先前研究相结合,表明持续抑制是 DTN 的一个定义特征。在此,我们讨论了使用尖峰计数和潜伏期测量神经元恢复时间的问题。我们还强调了持续抑制如何决定神经恢复时间,并作为人类前导效应的潜在机制。最后,我们探讨了恢复时间对蝙蝠听觉和回声定位中 DTN 的影响。