Lumley Lucille, Du Fu, Marrero-Rosado Brenda, Stone Michael, Keith Zora-Maya, Schultz Caroline, Whitten Kimberly, Walker Katie, Acon-Chen Cindy, Wright Linnzi, Shih Tsung-Ming
U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD, United States.
FD NeuroTechnologies, Inc., Columbia, MD, United States.
Toxicol Rep. 2021 Apr 19;8:896-907. doi: 10.1016/j.toxrep.2021.04.005. eCollection 2021.
Animal models are essential for evaluating the toxicity of chemical warfare nerve agents (CWNAs) to extrapolate to human risk and are necessary to evaluate the efficacy of medical countermeasures. The Göttingen minipig is increasingly used for toxicological studies because it has anatomical and physiological characteristics that are similar to those of humans. Our objective was to determine whether the minipig would be a useful large animal model to evaluate the toxic effects of soman (GD). We determined the intramuscular (IM) median lethal dose (LD) of GD in adult male Göttingen minipigs using an up-and-down dosing method. In addition to lethality estimates, we characterized the observable signs of toxicity, blood and tissue cholinesterase (ChE) activity and brain pathology following GD exposure. The 24 h LD of GD was estimated to be 4.7 μg/kg, with 95 % confidence limits of 3.6 and 6.3 μg/kg. As anticipated, GD inhibited ChE activity in blood and several tissues. Neurohistopathological analysis showed neurodegeneration and neuroinflammation in survivors exposed to 4.7 μg/kg of GD, including in the primary visual cortex and various thalamic nuclei. These findings suggest that the minipig will be a useful large animal model for assessing drugs to mitigate neuropathological effects of exposure to CWNAs.
动物模型对于评估化学战神经毒剂(CWNA)的毒性以推断人类风险至关重要,并且对于评估医学对策的疗效也是必要的。哥廷根小型猪越来越多地用于毒理学研究,因为它具有与人类相似的解剖学和生理学特征。我们的目的是确定小型猪是否会成为评估梭曼(GD)毒性作用的有用大型动物模型。我们使用上下剂量法确定了成年雄性哥廷根小型猪中GD的肌肉注射(IM)半数致死剂量(LD)。除了致死率估计外,我们还对GD暴露后的毒性可观察体征、血液和组织胆碱酯酶(ChE)活性以及脑病理学进行了表征。GD的24小时LD估计为4.7μg/kg,95%置信限为3.6和6.3μg/kg。正如预期的那样,GD抑制了血液和几种组织中的ChE活性。神经组织病理学分析显示,暴露于4.7μg/kg GD的幸存者出现神经退行性变和神经炎症,包括在初级视觉皮层和各种丘脑核中。这些发现表明,小型猪将成为评估减轻接触CWNA所致神经病理效应药物的有用大型动物模型。