Korn Henri, Faure Philippe
CNRS 2182, Institut Pasteur, 25, rue du Docteur-Roux, 75724 Paris, France.
C R Biol. 2003 Sep;326(9):787-840. doi: 10.1016/j.crvi.2003.09.011.
The search for chaotic patterns has occupied numerous investigators in neuroscience, as in many other fields of science. Their results and main conclusions are reviewed in the light of the most recent criteria that need to be satisfied since the first descriptions of the surrogate strategy. The methods used in each of these studies have almost invariably combined the analysis of experimental data with simulations using formal models, often based on modified Huxley and Hodgkin equations and/or of the Hindmarsh and Rose models of bursting neurons. Due to technical limitations, the results of these simulations have prevailed over experimental ones in studies on the nonlinear properties of large cortical networks and higher brain functions. Yet, and although a convincing proof of chaos (as defined mathematically) has only been obtained at the level of axons, of single and coupled cells, convergent results can be interpreted as compatible with the notion that signals in the brain are distributed according to chaotic patterns at all levels of its various forms of hierarchy. This chronological account of the main landmarks of nonlinear neurosciences follows an earlier publication [Faure, Korn, C. R. Acad. Sci. Paris, Ser. III 324 (2001) 773-793] that was focused on the basic concepts of nonlinear dynamics and methods of investigations which allow chaotic processes to be distinguished from stochastic ones and on the rationale for envisioning their control using external perturbations. Here we present the data and main arguments that support the existence of chaos at all levels from the simplest to the most complex forms of organization of the nervous system. We first provide a short mathematical description of the models of excitable cells and of the different modes of firing of bursting neurons (Section 1). The deterministic behavior reported in giant axons (principally squid), in pacemaker cells, in isolated or in paired neurons of Invertebrates acting as coupled oscillators is then described (Section 2). We also consider chaotic processes exhibited by coupled Vertebrate neurons and of several components of Central Pattern Generators (Section 3). It is then shown that as indicated by studies of synaptic noise, deterministic patterns of firing in presynaptic interneurons are reliably transmitted, to their postsynaptic targets, via probabilistic synapses (Section 4). This raises the more general issue of chaos as a possible neuronal code and of the emerging concept of stochastic resonance Considerations on cortical dynamics and of EEGs are divided in two parts. The first concerns the early attempts by several pioneer authors to demonstrate chaos in experimental material such as the olfactory system or in human recordings during various forms of epilepsies, and the belief in 'dynamical diseases' (Section 5). The second part explores the more recent period during which surrogate-testing, definition of unstable periodic orbits and period-doubling bifurcations have been used to establish more firmly the nonlinear features of retinal and cortical activities and to define predictors of epileptic seizures (Section 6). Finally studies of multidimensional systems have founded radical hypothesis on the role of neuronal attractors in information processing, perception and memory and two elaborate models of the internal states of the brain (i.e. 'winnerless competition' and 'chaotic itinerancy'). Their modifications during cognitive functions are given special attention due to their functional and adaptive capabilities (Section 7) and despite the difficulties that still exist in the practical use of topological profiles in a state space to identify the physical underlying correlates. The reality of 'neurochaos' and its relations with information theory are discussed in the conclusion (Section 8) where are also emphasized the similarities between the theory of chaos and that of dynamical systems. Both theories strongly challenge computationalism and suggest that new models are needed to describe how the external world is represented in the brain.
与许多其他科学领域一样,对混沌模式的探索吸引了神经科学领域的众多研究者。根据自首次描述替代策略以来需要满足的最新标准,对他们的研究结果和主要结论进行了综述。这些研究中使用的方法几乎总是将实验数据分析与使用形式模型的模拟相结合,这些模型通常基于修改后的赫胥黎和霍奇金方程以及/或者爆发神经元的欣德马什和罗斯模型。由于技术限制,在关于大型皮层网络的非线性特性和高级脑功能的研究中,这些模拟结果比实验结果更具说服力。然而,尽管仅在轴突、单个和耦合细胞水平上获得了令人信服的混沌(如数学定义)证据,但收敛结果可以解释为与以下观点一致:大脑中的信号在其各种层次结构的所有层面上都是按照混沌模式分布的。对非线性神经科学主要里程碑的这一按时间顺序的叙述,遵循了一篇早期出版物[福尔,科恩,《法国科学院院报》,第三系列324 (2001) 773 - 793],该出版物侧重于非线性动力学的基本概念以及使混沌过程能够与随机过程区分开来的研究方法,以及设想使用外部扰动对其进行控制的基本原理。在这里,我们展示支持从最简单到最复杂形式的神经系统组织层面存在混沌的数据和主要论据。我们首先对可兴奋细胞模型以及爆发神经元的不同放电模式进行简短的数学描述(第1节)。然后描述在巨大轴突(主要是鱿鱼的)、起搏器细胞、作为耦合振荡器的无脊椎动物的孤立或成对神经元中报告的确定性行为(第2节)。我们还考虑耦合的脊椎动物神经元以及中枢模式发生器的几个组成部分所表现出的混沌过程(第3节)。然后表明,正如突触噪声研究所示,突触前中间神经元中确定性的放电模式通过概率性突触可靠地传递给它们的突触后靶标(第4节)。这就提出了一个更普遍的问题,即混沌作为一种可能的神经元编码以及随机共振这一新兴概念。关于皮层动力学和脑电图的讨论分为两部分。第一部分涉及几位先驱作者早期试图在诸如嗅觉系统等实验材料中或在各种形式癫痫发作期间的人类记录中证明混沌,以及对“动态疾病”的信念(第5节)。第二部分探讨了更近的时期,在此期间替代测试、不稳定周期轨道的定义和倍周期分岔已被用于更牢固地确立视网膜和皮层活动的非线性特征,并定义癫痫发作的预测指标(第6节)。最后,对多维系统的研究基于神经元吸引子在信息处理、感知和记忆中的作用以及大脑内部状态的两个精细模型(即“无胜者竞争”和“混沌游走”)提出了激进的假设。由于它们的功能和适应能力,特别关注它们在认知功能过程中的变化(第7节),尽管在实际使用状态空间中的拓扑轮廓来识别潜在的物理相关物方面仍然存在困难。结论部分(第8节)讨论了“神经混沌”的现实及其与信息理论的关系,其中还强调了混沌理论与动力系统理论之间的相似性。这两种理论都对计算主义提出了强烈挑战,并表明需要新的模型来描述外部世界在大脑中是如何被表征的。