From the Department of Physiology and Biophysics (M.R.A., D.A., C.V.G., C.W.C.) Department of Pharmacology and Experimental Therapeutics, Photonics Center (C.V.G.), Boston University School of Medicine, Boston, Massachusetts Department of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts (J.F., M.A.) Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Boston, Massachusetts (C.W.C.).
Anesthesiology. 2018 Oct;129(4):733-743. doi: 10.1097/ALN.0000000000002342.
WHAT THIS ARTICLE TELLS US THAT IS NEW: BACKGROUND:: Previous work on the action of volatile anesthetics has focused at either the molecular level or bulk neuronal measurement such as electroencephalography or functional magnetic resonance imaging. There is a distinct gulf in resolution at the level of cellular signaling within neuronal systems. The authors hypothesize that anesthesia is caused by induced dyssynchrony in cellular signaling rather than suppression of individual neuron activity.
Employing confocal microscopy and Caenorhabditis elegans expressing the calcium-sensitive fluorophore GCaMP6s in specific command neurons, the authors measure neuronal activity noninvasively and in parallel within the behavioral circuit controlling forward and reverse crawling. The authors compare neuronal dynamics and coordination in a total of 31 animals under atmospheres of 0, 4, and 8% isoflurane.
When not anesthetized, the interneurons controlling forward or reverse crawling occupy two possible states, with the activity of the "reversal" neurons AVA, AVD, AVE, and RIM strongly intercorrelated, and the "forward" neuron AVB anticorrelated. With exposure to 4% isoflurane and onset of physical quiescence, neuron activity wanders rapidly and erratically through indeterminate states. Neuron dynamics shift toward higher frequencies, and neuron pair correlations within the system are reduced. At 8% isoflurane, physical quiescence continues as neuronal signals show diminished amplitude with little correlation between neurons. Neuronal activity was further studied using statistical tools from information theory to quantify the type of disruption caused by isoflurane. Neuronal signals become noisier and more disordered, as measured by an increase in the randomness of their activity (Shannon entropy). The coordination of the system, measured by whether information exhibited in one neuron is also exhibited in other neurons (multiinformation), decreases significantly at 4% isoflurane (P = 0.00015) and 8% isoflurane (P = 0.0028).
The onset of anesthesia corresponds with high-frequency randomization of individual neuron activity coupled with induced dyssynchrony and loss of coordination between neurons that disrupts functional signaling.
关于这个主题,我们已经知道什么:这篇文章告诉我们什么是新的:背景:先前关于挥发性麻醉剂作用的工作集中在分子水平或整体神经元测量,如脑电图或功能磁共振成像。在神经元系统的细胞信号水平上存在明显的分辨率差距。作者假设麻醉是由细胞信号诱导的失同步引起的,而不是单个神经元活动的抑制。
作者采用共聚焦显微镜和在特定命令神经元中表达钙敏感荧光蛋白 GCaMP6s 的秀丽隐杆线虫,非侵入性地测量控制前进和后退爬行的行为回路中的神经元活动。作者在总共 31 只动物的 0、4 和 8%异氟醚气氛下比较神经元动力学和协调。
在未麻醉状态下,控制前进或后退爬行的中间神经元占据两个可能的状态,“反转”神经元 AVA、AVD、AVE 和 RIM 的活动强烈相关,而“前进”神经元 AVB 呈反相关。暴露于 4%异氟醚并开始物理静止时,神经元活动迅速而不稳定地在不确定状态中波动。神经元动力学向更高频率转移,系统内神经元对的相关性降低。在 8%异氟醚下,随着神经元信号的幅度减小,神经元之间的相关性降低,物理静止继续,神经元信号显示出减小的幅度。作者进一步使用信息论的统计工具研究神经元活动,以量化异氟醚引起的破坏类型。神经元信号变得更加嘈杂和无序,如通过其活动的随机性(香农熵)增加来衡量。系统的协调,即一个神经元中显示的信息是否也显示在其他神经元中(多信息),在 4%异氟醚(P=0.00015)和 8%异氟醚(P=0.0028)时显著降低。
麻醉的开始与单个神经元活动的高频随机化以及神经元之间诱导的失步和协调丧失相关,这破坏了功能信号。