Klemm W R, Sherry C J
Int J Neurosci. 1981;14(1-2):15-33. doi: 10.3109/00207458108985812.
Summarized herein is the evidence that supports the hypothesis that neuronal action potentials (spike trains) are coded not only in terms of simple discharge rate but also can be serially coded by certain patterns of spike intervals. Based on the relative interval description method of Sherry and Marczynski (1972), our analyses of single-unit activity from cerebellar cortex neurons of rats seem to support three principal categories of conclusions; (1) Serial dependence of intervals does exist. This has been demonstrated with a variety of conventional statistical tests. These serial dependencies have also been shown to be independent of the (nonsequential) interval distribution variability. (2) Information theory is appropriate for evaluating spike trains. We have developed and tested methods for computing a fractional entropy for a given number of adjacent intervals, for assessing the relative fractional entropy of any one interval in a set of intervals, for computing for a group of neurons the mean and standard deviation of fractional entropy for specified clusters or intervals, and for transforming these values so that interval clusters of differing number can all be compared on the same numerical entropy scale (percentage maximum fractional entropy). In addition to the descriptive and quantitative value of such measures, we have also demonstrated their utility in testing hypotheses and in making empirical correlations. (3) The nervous system seems to process spike train intervals in "bytes", not "hits", of adjacent, serially ordered intervals. Among the several lines of evidence for this conclusion is the demonstration that drug-induced (ethanol) changes in fractional entropy of specific interval clusters seem to involve a "linked" combination of certain interval clusters, some which increase and others which decrease in incidence. Also, by using n-dimensional Chi-Square methodology, we have demonstrated that the relationships of adjacent intervals represent a Markovian process in which the duration of a given interval is partially determined by the duration of as many as four immediately preceding intervals. Finally, we showed that the relative fractional entropy (% maximum) of interval clusters of different numbers does not have a Gaussian distribution but rather is distributed in surprising ways by the specific number and relative durations of adjacent intervals. So just what is the serial ordering and information content of spike train intervals trying to tell us?. Perhaps it is trying to say that the nervous system processes information on a moment-by-moment basis in terms of "bytes" of short sequences of spikes with specific patterns of relative interspike durations. If so, we should be able to identify and characterize those "bytes". Much further testing must be done before we can claim that "neural codes" operate on the principles described herein. Nonetheless, we have made the issues explicit, and in our opinion have provided enough evidence to warrant further investigation.
神经元动作电位(脉冲序列)不仅根据简单放电率进行编码,还可以通过特定的脉冲间隔模式进行序列编码。基于Sherry和Marczynski(1972)的相对间隔描述方法,我们对大鼠小脑皮质神经元的单单位活动分析似乎支持三类主要结论:(1)间隔的序列依赖性确实存在。这已通过多种传统统计测试得到证明。这些序列依赖性也已被证明与(非顺序的)间隔分布变异性无关。(2)信息论适用于评估脉冲序列。我们已经开发并测试了用于计算给定数量相邻间隔的分数熵的方法,用于评估一组间隔中任何一个间隔的相对分数熵的方法,用于计算一组神经元的指定簇或间隔的分数熵的均值和标准差的方法,以及用于转换这些值以便不同数量的间隔簇都可以在相同的数值熵尺度(最大分数熵百分比)上进行比较的方法。除了这些测量的描述性和定量价值外,我们还证明了它们在检验假说和进行实证相关性方面的效用。(3)神经系统似乎以相邻、顺序排列的间隔的“字节”而非“命中数”来处理脉冲序列间隔。支持这一结论的几条证据之一是,药物诱导(乙醇)导致特定间隔簇的分数熵变化似乎涉及某些间隔簇的“连锁”组合,其中一些簇的发生率增加而另一些簇则减少。此外,通过使用n维卡方方法,我们证明了相邻间隔的关系代表一个马尔可夫过程,其中给定间隔的持续时间部分由多达四个紧接在前的间隔的持续时间决定。最后,我们表明不同数量的间隔簇的相对分数熵(最大百分比)不具有高斯分布,而是以相邻间隔的特定数量和相对持续时间以令人惊讶的方式分布。那么脉冲序列间隔的序列排序和信息内容究竟想告诉我们什么呢?也许它试图表明神经系统在逐个时刻根据具有特定相对脉冲间隔模式的短脉冲序列“字节”来处理信息。如果是这样,我们应该能够识别并表征那些“字节”。在我们能够声称“神经编码”按照本文所述的原则运行之前,还必须进行更多测试。尽管如此,我们已经明确了这些问题,并认为已经提供了足够的证据来 warrant进一步研究。(注:“warrant”此处结合语境大致可理解为“使有必要、值得”,但直接翻译可能较生硬且不易理解,所以译文保留了英文)