Freidin Dor, Har-Even Meirav, Rubovitch Vardit, Murray Kathleen E, Maggio Nicola, Shavit-Stein Efrat, Keidan Lee, Citron Bruce A, Pick Chaim G
Department of Anatomy and Anthropology, Sackler School of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.
Laboratory of Molecular Biology, VA New Jersey Health Care System, Research & Development, East Orange, NJ 07018, USA.
Biomedicines. 2023 May 19;11(5):1481. doi: 10.3390/biomedicines11051481.
Traumatic brain injury (TBI) is considered the most common neurological disorder among people under the age of 50. In modern combat zones, a combination of TBI and organophosphates (OP) can cause both fatal and long-term effects on the brain. We utilized a mouse closed-head TBI model induced by a weight drop device, along with OP exposure to paraoxon. Spatial and visual memory as well as neuron loss and reactive astrocytosis were measured 30 days after exposure to mild TBI (mTBI) and/or paraoxon. Molecular and cellular changes were assessed in the temporal cortex and hippocampus. Cognitive and behavioral deficits were most pronounced in animals that received a combination of paraoxon exposure and mTBI, suggesting an additive effect of the insults. Neuron survival was reduced in proximity to the injury site after exposure to paraoxon with or without mTBI, whereas in the dentate gyrus hilus, cell survival was only reduced in mice exposed to paraoxon prior to sustaining a mTBI. Neuroinflammation was increased in the dentate gyrus in all groups exposed to mTBI and/or to paraoxon. Astrocyte morphology was significantly changed in mice exposed to paraoxon prior to sustaining an mTBI. These results provide further support for assumptions concerning the effects of OP exposure following the Gulf War. This study reveals additional insights into the potentially additive effects of OP exposure and mTBI, which may result in more severe brain damage on the modern battlefield.
创伤性脑损伤(TBI)被认为是50岁以下人群中最常见的神经系统疾病。在现代作战区域,TBI与有机磷酸酯(OP)共同作用可对大脑造成致命和长期影响。我们使用重物下落装置诱导的小鼠闭合性颅脑损伤模型,并让其接触对氧磷。在轻度创伤性脑损伤(mTBI)和/或对氧磷暴露30天后,测量空间和视觉记忆以及神经元损失和反应性星形胶质细胞增生情况。对颞叶皮质和海马体进行分子和细胞变化评估。认知和行为缺陷在同时接受对氧磷暴露和mTBI的动物中最为明显,表明这些损伤具有累加效应。无论是否存在mTBI,暴露于对氧磷后,损伤部位附近的神经元存活率都会降低,而在齿状回门区,只有在遭受mTBI之前暴露于对氧磷的小鼠中细胞存活率才会降低。在所有暴露于mTBI和/或对氧磷的组中,齿状回的神经炎症均增加。在遭受mTBI之前暴露于对氧磷的小鼠中,星形胶质细胞形态发生了显著变化。这些结果为有关海湾战争后OP暴露影响的假设提供了进一步支持。这项研究揭示了关于OP暴露和mTBI潜在累加效应的更多见解,这可能会在现代战场上导致更严重的脑损伤。