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A multiscale approach to blast neurotrauma modeling: Part II: Methodology for inducing blast injury to in vitro models

Publication ,  Journal Article
Effgen, GB; Hue, CD; Vogel, E; Panzer, MB; Meaney, DF; Bass, CR; Morrison, B
Published in: Frontiers in Neurology
September 12, 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±6.9kPa-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. © 2012 Effgen, Hue, Vogel, Panzer, Meaney, Bass and Morrison.

Duke Scholars

Published In

Frontiers in Neurology

DOI

EISSN

1664-2295

Publication Date

September 12, 2012

Volume

FEB

Start / End Page

1 / 10

Related Subject Headings

  • 5202 Biological psychology
  • 3209 Neurosciences
  • 3202 Clinical sciences
  • 1701 Psychology
  • 1109 Neurosciences
  • 1103 Clinical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
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Effgen, G. B., Hue, C. D., Vogel, E., Panzer, M. B., Meaney, D. F., Bass, C. R., & Morrison, B. (2012). A multiscale approach to blast neurotrauma modeling: Part II: Methodology for inducing blast injury to in vitro models. Frontiers in Neurology, FEB, 1–10. https://doi.org/10.3389/fneur.2012.00023
Effgen, G. B., C. D. Hue, E. Vogel, M. B. Panzer, D. F. Meaney, C. R. Bass, and B. Morrison. “A multiscale approach to blast neurotrauma modeling: Part II: Methodology for inducing blast injury to in vitro models.” Frontiers in Neurology FEB (September 12, 2012): 1–10. https://doi.org/10.3389/fneur.2012.00023.
Effgen GB, Hue CD, Vogel E, Panzer MB, Meaney DF, Bass CR, et al. A multiscale approach to blast neurotrauma modeling: Part II: Methodology for inducing blast injury to in vitro models. Frontiers in Neurology. 2012 Sep 12;FEB:1–10.
Effgen, G. B., et al. “A multiscale approach to blast neurotrauma modeling: Part II: Methodology for inducing blast injury to in vitro models.” Frontiers in Neurology, vol. FEB, Sept. 2012, pp. 1–10. Scopus, doi:10.3389/fneur.2012.00023.
Effgen GB, Hue CD, Vogel E, Panzer MB, Meaney DF, Bass CR, Morrison B. A multiscale approach to blast neurotrauma modeling: Part II: Methodology for inducing blast injury to in vitro models. Frontiers in Neurology. 2012 Sep 12;FEB:1–10.

Published In

Frontiers in Neurology

DOI

EISSN

1664-2295

Publication Date

September 12, 2012

Volume

FEB

Start / End Page

1 / 10

Related Subject Headings

  • 5202 Biological psychology
  • 3209 Neurosciences
  • 3202 Clinical sciences
  • 1701 Psychology
  • 1109 Neurosciences
  • 1103 Clinical Sciences