Genetic Differences Modify Anesthetic Preconditioning of Traumatic Brain Injury in Drosophila.

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY
Dena Johnson-Schlitz, Amanda R Seidl, Zachariah P G Olufs, Wen Huang, David A Wassarman, Misha Perouansky
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Abstract

Pre-clinical vertebrate models of traumatic brain injury (TBI) routinely use anesthetics for animal welfare; however, humans experience TBI without anesthetics. Therefore, translation of findings from vertebrate models to humans hinges on understanding how anesthetics influence cellular and molecular events that lead to secondary injuries following TBI. To investigate the effects of anesthetics on TBI outcomes, we used an invertebrate Drosophila melanogaster model to compare outcomes between animals exposed or not exposed to anesthetics prior to the same primary injury. Using a common laboratory fly line, w1118, we found that exposure to the volatile anesthetics isoflurane or sevoflurane, but not ether, prior to TBI produced a dose-dependent reduction in mortality within 24 h following TBI. Thus, isoflurane and sevoflurane precondition w1118 flies to deleterious effects of TBI. To examine the effects of genetic differences on anesthetic preconditioning of TBI, we repeated the experiment with the Drosophila Genetic Reference Panel (DGRP) collection of genetically diverse, inbred fly lines. Pre-exposure to either isoflurane or sevoflurane revealed a wide range of preconditioning levels among 171 and 144 DGRP lines, respectively, suggesting a genetic component for variation in anesthetic preconditioning of mortality following TBI. Finally, genome-wide association study analyses identified single-nucleotide polymorphisms in genes associated with isoflurane or sevoflurane preconditioning of TBI. Several of the genes, including the fly ortholog of mammalian Calcium Voltage-Gated Subunit Alpha1 D (CACNA1D), are highly expressed in neurons and are functionally linked to both anesthetics and TBI. These data indicate that anesthetic dose and genetic background should be considered when investigating effects of anesthetics in vertebrate TBI models, and they support use of the fly model for elucidating the mechanisms underlying anesthetic preconditioning of TBI.

遗传差异可改变果蝇创伤性脑损伤的麻醉预处理。
创伤性脑损伤(TBI)的脊椎动物临床前模型通常使用麻醉剂,以保障动物福利;然而,人类在经历 TBI 时却不使用麻醉剂。因此,将脊椎动物模型的研究结果转化为人类的研究结果取决于了解麻醉剂如何影响细胞和分子事件,从而导致创伤性脑损伤后的继发性损伤。为了研究麻醉剂对创伤性脑损伤结果的影响,我们使用了无脊椎动物黑腹果蝇模型来比较在相同的原发性损伤之前暴露或未暴露于麻醉剂的动物之间的结果。通过使用一种常见的实验蝇品系 w1118,我们发现在创伤性脑损伤前接触异氟醚或七氟醚等挥发性麻醉剂(而非乙醚)会使创伤性脑损伤后 24 小时内的死亡率呈剂量依赖性下降。因此,异氟烷和七氟烷可使w1118苍蝇在创伤性脑损伤后出现有害影响。为了研究基因差异对创伤性脑损伤麻醉预处理的影响,我们用果蝇基因参考组(DGRP)收集的基因多样的近交系果蝇重复了该实验。在预暴露于异氟醚或七氟烷的情况下,171 个 DGRP 品系和 144 个 DGRP 品系的预处理水平差异很大,这表明创伤性脑损伤后死亡率的麻醉预处理存在遗传因素。最后,全基因组关联研究分析发现了与异氟烷或七氟烷对创伤性脑损伤的预处理相关的单核苷酸多态性基因。其中几个基因,包括哺乳动物钙电压门控亚基 Alpha1 D(CACNA1D)的苍蝇同源基因,在神经元中高度表达,在功能上与麻醉剂和创伤性脑损伤有关。这些数据表明,在研究麻醉剂对脊椎动物创伤性脑损伤模型的影响时,应考虑麻醉剂的剂量和遗传背景,并支持使用苍蝇模型来阐明创伤性脑损伤的麻醉预处理机制。
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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来源期刊
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
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