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食虫蝙蝠大足鼠耳蝠听觉系统中目标距离编码的可能神经机制。

Possible neural mechanisms of target distance coding in auditory system of the echolocating bat Myotis lucifugus.

作者信息

Sullivan W E

出版信息

J Neurophysiol. 1982 Oct;48(4):1033-47. doi: 10.1152/jn.1982.48.4.1033.

Abstract
  1. In order to investigate the possible neural mechanisms underlying delay-dependent facilitation in the bat's auditory cortex (18), the responses to single FM pulses of varying amplitude were examined. Analysis of amplitude-spike count functions revealed three distinct types: monotonic, simple nonmonotonic, and complex nonmonotonic. The complex nonmonotonic function had two separate amplitude peaks, with a clear notch or worst amplitude between them. Other units had spike count functions that were mainly monotonic or nonmonotonic, but showed some evidence for a second response region. 2. Examination of response latency revealed another novel response property, which has been termed the paradoxical latency shift. Units with this response property responded at a shorter latency to sounds of low amplitude than to sounds of high amplitude. The paradoxical latency shift also appears to be related to the twin-peaked complex nonmonotonic response function. Units with the most prominent twin-peaked response functions also had the clearest latency shifts. In these units, the high-amplitude peak corresponded to the long-latency response and the low-amplitude peak to the short-latency-response. 3. These curious spike count and latency observations can be explained if they are considered in relation to the temporal and amplitude pattern of the acoustic input during echolocation. In echolocation, a loud orientation pulse is followed by a weaker echo. In delay-dependent facilitation, this pulse-echo sequence is followed by a neural response if the pulse-echo delay is appropriate. The simplest model for delay-dependent facilitation assumes that a synchronization of excitatory inputs from the pulse and echo is needed for facilitation. Since the weaker echo occurs after the pulse, it is closer in time to the postulated synchronization point. Therefore, in order for this model to work, the echo input must reach the summation place with less of a time lag than the pulse input. This is exactly what is seen with the paradoxical latency shift; the loud "pulse" response is delayed relative to the weak "echo" response.
摘要
  1. 为了研究蝙蝠听觉皮层中与延迟相关的易化作用潜在的神经机制(18),我们检测了对不同幅度单频调频脉冲的反应。对幅度 - 放电计数函数的分析揭示了三种不同类型:单调型、简单非单调型和复杂非单调型。复杂非单调函数有两个独立的幅度峰值,它们之间有明显的波谷或最差幅度。其他神经元的放电计数函数主要是单调或非单调的,但也有一些证据表明存在第二个反应区域。2. 对反应潜伏期的检测揭示了另一种新的反应特性,即矛盾潜伏期偏移。具有这种反应特性的神经元对低幅度声音的反应潜伏期比对高幅度声音的反应潜伏期短。矛盾潜伏期偏移似乎也与双峰复杂非单调反应函数有关。具有最显著双峰反应函数的神经元也有最明显的潜伏期偏移。在这些神经元中,高幅度峰值对应长潜伏期反应,低幅度峰值对应短潜伏期反应。3. 如果将这些奇怪的放电计数和潜伏期观察结果与回声定位期间声学输入的时间和幅度模式联系起来考虑,可以得到解释。在回声定位中,一个响亮的定向脉冲之后跟着一个较弱的回声。在与延迟相关的易化作用中,如果脉冲 - 回声延迟合适,这个脉冲 - 回声序列之后会跟着一个神经反应。与延迟相关的易化作用的最简单模型假设,为了实现易化,需要来自脉冲和回声的兴奋性输入同步。由于较弱的回声在脉冲之后出现,它在时间上更接近假定的同步点。因此,为了使这个模型起作用,回声输入到达总和位置的时间延迟必须比脉冲输入小。这正是矛盾潜伏期偏移中所看到的情况;响亮的“脉冲”反应相对于微弱的“回声”反应延迟了。

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