Effgen Gwen B, Hue Christopher D, Vogel Edward, Panzer Matthew B, Meaney David F, Bass Cameron R, Morrison Barclay
Department of Biomedical Engineering, Columbia University New York, NY, USA.
Front Neurol. 2012 Feb 24;3:23. doi: 10.3389/fneur.2012.00023. eCollection 2012.
Due to the prominent role of improvised explosive devices (IEDs) in wounding patterns of U.S. war-fighters in Iraq and Afghanistan, blast injury has risen to a new level of importance and is recognized to be a major cause of injuries to the brain. However, an injury risk-function for microscopic, macroscopic, behavioral, and neurological deficits has yet to be defined. While operational blast injuries can be very complex and thus difficult to analyze, a simplified blast injury model would facilitate studies correlating biological outcomes with blast biomechanics to define tolerance criteria. Blast-induced traumatic brain injury (bTBI) results from the translation of a shock wave in-air, such as that produced by an IED, into a pressure wave within the skull-brain complex. Our blast injury methodology recapitulates this phenomenon in vitro, allowing for control of the injury biomechanics via a compressed-gas shock tube used in conjunction with a custom-designed, fluid-filled receiver that contains the living culture. The receiver converts the air shock wave into a fast-rising pressure transient with minimal reflections, mimicking the intracranial pressure history in blast. We have developed an organotypic hippocampal slice culture model that exhibits cell death when exposed to a 530 ± 17.7-kPa peak overpressure with a 1.026 ± 0.017-ms duration and 190 ± 10.7 kPa-ms impulse in-air. We have also injured a simplified in vitro model of the blood-brain barrier, which exhibits disrupted integrity immediately following exposure to 581 ± 10.0 kPa peak overpressure with a 1.067 ± 0.006-ms duration and 222 ± 6.9 kPa-ms impulse in-air. To better prevent and treat bTBI, both the initiating biomechanics and the ensuing pathobiology must be understood in greater detail. A well-characterized, in vitro model of bTBI, in conjunction with animal models, will be a powerful tool for developing strategies to mitigate the risks of bTBI.
由于简易爆炸装置(IED)在美国驻伊拉克和阿富汗作战人员的受伤模式中扮演着突出角色,爆炸伤已上升到一个新的重要程度,并被公认为是脑部受伤的主要原因。然而,针对微观、宏观、行为和神经功能缺损的损伤风险函数尚未确定。虽然作战爆炸伤可能非常复杂,因此难以分析,但简化的爆炸伤模型将有助于开展研究,将生物学结果与爆炸生物力学相关联,以确定耐受标准。爆炸所致创伤性脑损伤(bTBI)是由空气中的冲击波(如简易爆炸装置产生的冲击波)转化为颅-脑复合体中的压力波而引起的。我们的爆炸伤研究方法在体外再现了这一现象,通过与定制设计的、装有活培养物的充液接收器配合使用的压缩气体激波管来控制损伤生物力学。该接收器将空气冲击波转换为上升迅速且反射最小的压力瞬变,模拟爆炸时的颅内压力变化过程。我们开发了一种器官型海马切片培养模型,当暴露于空气中峰值超压为530±17.7kPa、持续时间为1.026±0.017ms且冲量为190±10.7kPa·ms时,该模型会出现细胞死亡。我们还损伤了一个简化的体外血脑屏障模型,该模型在暴露于空气中峰值超压为581±10.0kPa、持续时间为1.067±0.006ms且冲量为222±6.9kPa·ms后,其完整性立即遭到破坏。为了更好地预防和治疗bTBI,必须更详细地了解引发损伤的生物力学以及随后的病理生物学过程。一个特征明确的bTBI体外模型,与动物模型相结合,将成为制定减轻bTBI风险策略的有力工具。