脑干中精确的尖峰计时信息与交流的需要和对环境声音的感知是一致的。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
Chris Scholes, Stephen Coombes, Alan R Palmer, William S Rhode, Rob Mill, Christian J Sumner
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引用次数: 0

摘要

声音振幅的动态波动,被称为声包络,在自然声音中无处不在,并传递对识别语音和一般声音至关重要的信息。我们在知觉上对最常见的慢调制最为敏感。然而,先前对脑干包膜编码的研究发现,这些缓慢、低频的调制没有得到充分的体现。具体来说,在某些神经元类型中,峰值时间与包膜的同步得到了增强,形成了专门用于包膜处理的通道,但被调谐到有限范围的快速、高频包膜(200-500 Hz)。在这里,我们使用猫的历史数据集表明,之前的分析对神经编码做出了强有力的假设,低估了低频包络的编码。虽然有些神经元对包膜的编码优于其他神经元,但大多数神经元对包膜频率的编码范围很广,并且在其精确的峰值时间模式中最准确地表示较慢的包膜波动。从峰值定时确定包络频率与可靠性以及峰值动态与时变包络的相互作用方式有关。在一些表现最好的神经元中,暂时复杂的“模式锁定”尖峰模式有助于增强包膜编码。第二个长期存在的矛盾是,神经包络编码在高声级时会退化,而包络感知在大声级范围内是稳健的。我们发现包络形状的峰值时间编码对于小群神经元具有水平鲁棒性。这些发现反驳了脑干中包膜的特征特定编码,并支持分布式人群峰值时间编码,其中与包膜的同步是一个不完整的描述。这个代码是准确的缓慢波动和稳健跨声级。因此,脑干中精确的尖峰计时信息毕竟与交流的需要和对环境声音的感知是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Precise spike-timing information in the brainstem is well aligned with the needs of communication and the perception of environmental sounds.

The dynamic fluctuations in the amplitude of sound, known as sound envelopes, are ubiquitous in natural sounds and convey information critical for the recognition of speech, and of sounds generally. We are perceptually most sensitive to slow modulations which are most common. However, previous studies of envelope coding in the brainstem found an under-representation of these slow, low-frequency, modulations. Specifically, the synchronization of spike times to the envelope was enhanced in some neuron types, forming channels specialized for envelope processing but tuned to a restricted range of fast, high-frequency, envelopes (200-500 Hz). Here, we show using a historical dataset from cats that previous analyses, which made strong assumptions about the neural code, underestimated the encoding of low-frequency envelopes. While some neurons encode envelope better than others, most encode a wide range of envelope frequencies, and represent slower envelope fluctuations most accurately in their precise patterns of spike times. Identification of envelope frequency from spike-timing was linked to reliability, and to the way that dynamics of spiking interacted with the time-varying envelope. In some of the best-performing neurons, temporally complex "mode-locked" spike patterns served to enhance envelope coding. A second long-standing contradiction was that neural envelope coding is degraded at high sound levels, whilst the perception of envelope is robust at a wide range of sound levels. We find that spike-time encoding of envelope shape becomes level-robust for small populations of neurons. These findings argue against feature-specific coding of envelopes in the brainstem, and for a distributed population spike-time code for which synchrony to the envelope is an incomplete description. This code is accurate for slow fluctuations and robust across sound level. Thus, precise spike-timing information in the brainstem is after-all aligned with the needs of communication and the perception of environmental sounds.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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