Department of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, USA.
Department of Medicine, University of Pennsylvania, Philadelphia, USA.
Sci Rep. 2020 Sep 25;10(1):15789. doi: 10.1038/s41598-020-72669-1.
The field of neuropharmacology has not yet achieved a full understanding of how the brain transitions between states of consciousness and drug-induced unconsciousness, or anesthesia. Many small molecules are used to alter human consciousness, but the repertoire of underlying molecular targets, and thereby the genes, are incompletely understood. Here we describe a robust larval zebrafish model of anesthetic action, from sedation to general anesthesia. We use loss of movement under three different conditions, spontaneous movement, electrical stimulation or a tap, as a surrogate for sedation and general anesthesia, respectively. Using these behavioral patterns, we find that larval zebrafish respond to inhalational and IV anesthetics at concentrations similar to mammals. Additionally, known sedative drugs cause loss of spontaneous larval movement but not to the tap response. This robust, highly tractable vertebrate model can be used in the detection of genes and neural substrates involved in the transition from consciousness to unconsciousness.
神经药理学领域尚未完全了解大脑如何在意识状态和药物诱导的无意识状态(即麻醉)之间转换。许多小分子被用于改变人类的意识,但潜在的分子靶点(以及由此产生的基因)还不完全清楚。在这里,我们描述了一个稳健的幼鱼斑马鱼麻醉作用模型,从镇静到全身麻醉。我们分别使用三种不同条件下的运动丧失(自发运动、电刺激或敲击)作为镇静和全身麻醉的替代物。使用这些行为模式,我们发现幼鱼斑马鱼对吸入和静脉麻醉剂的反应与哺乳动物相似。此外,已知的镇静药物会导致幼鱼的自发运动丧失,但不会导致敲击反应。这种稳健、高度可操作的脊椎动物模型可用于检测参与从意识向无意识转变的基因和神经基质。