In vivo Quantification of Neural Criticality and Complexity in Mouse Cortex and Striatum in a Model of Cocaine Abstinence.

Wesley C Smith
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Abstract

Self-organized criticality is a hallmark of complex dynamic systems at phase transitions. Systems that operate at or near criticality have large-scale fluctuations or "avalanches", the frequency and duration power of which are best fit with a power law revealing them to be scale-free and fractal, and such power laws are ubiquitous. It is an attractive concept in neuroscience since spiking avalanches are exhibited by neural tissue, and may underpin how minuscule events could scale up to circuits and provide adaptive psychobiological function. Much is yet to be understood about criticality in vivo in the healthy brain and in disorders such as addiction, as drugs may alter the critical state's "tuning" to generate drug seeking and dysphoria. Thus, here a novel toolset was developed to use neural avalanches and their self-similarity, rather than power law fit slope exponents as is canonically done, to quantify criticality in a previously collected high-density electrophysiological in vivo corticostriatal dataset from a mouse model of early cocaine abstinence. During behavioral quiescence, in the prefrontal cortex but not ventral striatum of cocaine-dosed mice, it was found that critical tuning is enhanced compared to drug-free controls. Additionally, an empirical biological demonstration of complexity's theoretical correlation to criticality was shown in drug-free mice, was exponentially enhanced in drug-treated cortex, but was absent in the drug-treated striatum. As shown, quantifying criticality grants experimental support for the "critical brain hypothesis" and allows for statistical interpretation of inter-subject variability and development of further testable hypotheses in systems neuroscience.

Significance statement: The "critical brain hypothesis" asserts neural networks are comparable to material in phase transitions at a critical point, their "avalanches" of system-wide spike bursts best seen in log-log plots of probability vs. avalanche size or duration, with slope following a scale-free or fractal power law. In discussing criticality, "critical tuning" is mentioned but quantification thereof left for later experimentation, despite being necessary for a scientific hypothesis. Presented are methods to quantify critical tuning through assessing similarity or fractalness among corticostriatal avalanches collected using high-density electrophysiology in cocaine-conditioned mice, along with an empirical in vivo confirmation of the mathematical concept that data complexity correlates with criticality. Interestingly, cocaine enhances critical tuning in cortex and aberrantly modifies complexity in a region-specific manner.

可卡因戒断模型小鼠皮层和纹状体神经临界性和复杂性的体内定量研究。
自组织临界性是复杂动态系统相变的标志。在临界或接近临界时运行的系统具有大规模波动或“雪崩”,其频率和持续时间的功率最适合幂律,表明它们是无标度和分形的,这种幂律无处不在。这是神经科学中一个有吸引力的概念,因为尖峰雪崩是由神经组织表现出来的,并且可能支持微小事件如何扩展到电路并提供适应性心理生物学功能。关于健康大脑和成瘾等疾病的体内临界状态,还有很多有待了解的地方,因为药物可能会改变临界状态的“调谐”,从而产生药物寻求和不安。因此,本文开发了一种新的工具集,用于使用神经雪崩及其自相似性,而不是像通常那样使用幂律拟合斜率指数,来量化先前从早期可卡因戒断小鼠模型中收集的高密度电生理体内皮质纹状体数据集的临界性。在行为静止期间,在服用可卡因的小鼠的前额叶皮层,而不是腹侧纹状体中,发现与未服用毒品的对照组相比,关键调谐增强。此外,在没有药物的小鼠中,复杂性与临界性的理论相关性的经验生物学证明,在药物治疗的小鼠皮层中呈指数级增强,但在药物治疗的纹状体中没有。如图所示,量化临界性为“关键脑假说”提供了实验支持,并允许对系统神经科学中学科间变异性的统计解释和进一步可测试假设的发展。意义声明:“关键大脑假说”断言神经网络与处于临界点相变的物质相当,它们的“雪崩”系统范围内的尖峰爆发最好在概率与雪崩大小或持续时间的对数对数图中看到,斜率遵循无标度或分形幂律。在讨论临界性时,提到了“临界调谐”,但将其量化留给以后的实验,尽管这是科学假设所必需的。提出了通过评估可卡因条件小鼠高密度电生理学收集的皮质纹状体雪崩的相似性或分形性来量化临界调谐的方法,以及数据复杂性与临界性相关的数学概念的经验体内证实。有趣的是,可卡因增强了大脑皮层的关键调节,并以特定区域的方式异常地改变了复杂性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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