BioMed Research International

BioMed Research International / 2017 / Article

Research Article | Open Access

Volume 2017 |Article ID 2075463 | 10 pages | https://doi.org/10.1155/2017/2075463

Protection against Blast-Induced Traumatic Brain Injury by Increase in Brain Volume

Academic Editor: Leyan Xu
Received12 Dec 2016
Revised13 Feb 2017
Accepted23 Mar 2017
Published10 Apr 2017

Abstract

Blast-induced traumatic brain injury (bTBI) is a leading cause of injuries in recent military conflicts and it is responsible for an increased number of civilian casualties by terrorist attacks. bTBI includes a variety of neuropathological changes depending on the intensity of blast overpressure (BOP) such as brain edema, neuronal degeneration, diffuse axonal damage, and vascular dysfunction with neurological manifestations of psychological and cognitive abnormalities. Internal jugular vein (IJV) compression is known to reduce intracranial compliance by causing an increase in brain volume and was shown to reduce brain damage during closed impact-induced TBI. We investigated whether IJV compression can attenuate signs of TBI in rats after exposure to BOP. Animals were exposed to three 110 ± 5 kPa BOPs separated by 30 min intervals. Exposure to BOP resulted in a significant decrease of neuronal nuclei (NeuN) together with upregulation of aquaporin-4 (AQP-4), 3-nitrotyrosine (3-NT), and endothelin 1 receptor A (ETRA) expression in frontal cortex and hippocampus one day following exposures. IJV compression attenuated this BOP-induced increase in 3-NT in cortex and ameliorated the upregulation of AQP-4 in hippocampus. These results suggest that elevated intracranial pressure and intracerebral volume have neuroprotective potential in blast-induced TBI.

1. Introduction

Traumatic brain injury (TBI) is of increasing concern in both military and civilian populations due to the long-term health problems and costs related to recovery from such injuries. In particular, blast-induced TBI (bTBI) has been classified as the “signature injury” of recent wars in Iraq and Afghanistan [13]. The neurological impairment in bTBI may result from different mechanisms including both a direct shock wave effect on brain and an indirect transfer of the shock wave through blood vessels and cerebrospinal fluid (CSF) to the brain [47]. Exposure to blast overpressure (BOP) initiates a cascade of cellular pathological processes in brain including damage to the microvasculature and blood-brain barrier (BBB) integrity, followed by increased BBB permeability [8, 9]. The breakdown of the BBB can result in brain edema and increase in intracranial pressure (ICP), accompanied by activation of secondary brain injury by impairing cerebral perfusion and oxygenation [10]. In particular, activation of oxidative mechanisms and neuroinflammation has been shown to contribute to the neurodegeneration and cell apoptosis in secondary brain injury following bTBI [11, 12].

Current treatment of acute TBI includes surgical intervention and supportive care therapies. Treatment of elevated ICP and optimizing cerebral perfusion are the cornerstones of current therapy [13]. Several attempts to minimize secondary brain injury after TBI by pharmacological intervention or hypothermia were ineffective in clinical trials [14]. So far, injury prevention remains the most efficient way for controlling TBI. Furthermore, it seems unlikely that any treatment aimed at injury reversal will be as effective as injury prevention. The preventive measures against bTBI include the use of personal protective equipment such as Kevlar vests or helmets. Even with an advanced helmet design, a significant part of the head remains exposed to the blast. The prevalent incidence of bTBI in recent military conflicts and the frequency of sports-related concussions indicate that the effectiveness of personal protective equipment against bTBI is insufficient [7, 15, 16].

Recently, it was suggested that increasing ICP and reducing slosh by compression of the internal jugular vein (IJV) markedly reduced markers of neurological injury in acceleration- deceleration TBI models [17, 18]. This finding suggests that the development of a neck collar as a potential protective tool against closed head TBI might be possible. The precise underlying mechanisms of bTBI, as well as the neuropathological, pathophysiological, and functional consequences of bTBI, remain unknown.

In the current study, we tested whether IJV compression could provide protection of brain tissue against blast-induced traumatic brain injury. It is still unknown if exposure to BOP or rapid acceleration due to impact is the leading transmission mode of injury [19]. A recent study in a mouse model by Gullotti et al. [20] reported that restricting the movement of the head significantly increased survivability and decreased cognitive deficits following blast exposure. Head immobilization was most effective against parallel exposure to the blast wave as opposed to a perpendicular orientation. In our study, we minimized linear/rotational head movement by head restriction and by exposing animal in the frontal (face-on) orientation to blast.

2. Materials and Methods

2.1. Animals and Exposure to BOP

Male Sprague-Dawley (SD) rats weighing 325–400 g (Taconic Farm, Hudson, NY) were used in the study. Immediately before exposure to BOP, animals were anesthetized with 5% isoflurane, secured in a holder placed inside a compressed air-driven shock tube, and subjected to BOP in frontal (face-on) orientation. The animals were restrained in the holder to ensure adequate immobilization during blast exposure. The animals were exposed to three  kPa exposures separated by 30 min and were allowed to recover from anesthesia after each exposure. The reference pressure outside the animal was measured by two piezoelectric sensors (PCB Piezotronics Inc., Buffalo, NY) placed on opposite sides at the level of rat’s head. One sensor was aligned parallel to the direction of propagation of BOP, measuring static pressure, while the other sensor was aligned perpendicular to the blast flow to measure reflected pressure. The sensors were connected to a signal conditioning unit which provided input to PowerLab and LabChart (AD Instruments, Colorado Springs, CO) for data acquisition (collection rate 100 kHz), display, and recording [21]. The values, expressed as average (standard error) for , of peak amplitude, duration, and impulse for positive excursion of static pressure (overpressure) were 110 (5.20) kPa, 7.82 (0.061) ms, and 356.93 (2.28) kPa·ms, respectively. The average () parameters of reflected pressure were peak pressure of 148.9 (0.73) kPa, overpressure duration of 7.93 (0.021) ms, and overpressure impulse of 615.338 (4.67) kPa·ms.

2.2. IJV Compression

The blood compartment is a single intracranial compartment that can be easily subjected to rapid changes in volume and pressure resulting in variation in the intracranial compliance. Mechanical obstruction of the veins in the neck inhibits the outflow of blood from the brain and increases ICP [17]. Mechanical obstruction by IJV compression was applied by tightening Velcro tape around the animal’s neck [17] without compromising the airway. The tape was placed on the rat’s neck for approximately one minute before BOP exposure. Immediately after exposure, the tape was removed from animals. The increase in ICP occurred within seconds following IJV compression. The parameters of compression were determined in a separate group of animals () which were not used for histopathology as an additional surgical procedure could interfere with neuropathological assessment. In that group an increase in ICP concurrent with IJV compression was confirmed by measuring ICP with a FISO pressure probe (FISO Technologies, Quebec City, Canada) which was placed in the lateral ventricle, as previously described [21]. The baseline ICP was  mmHg and was increased to  mmHg following IJV compression ().

2.3. Animal Grouping

Animals were randomly assigned to three groups ( in each group): one control group (Con) without exposure to BOP and two blast groups: one group without IJV compression (Blast) and a second group with IJV compression (I-Blast). All groups were treated identically including receiving anesthesia and being placed in the blast tube. One day following exposure, the rats were euthanized with Euthasol (Virbac AH, Inc., Fort Worth, TX) and brain tissues were removed and fixed with 10% formalin.

2.4. Histology and Immunohistochemistry

Brain tissues fixed in 10% formalin were embedded in paraffin. Coronal sections (5 μm) were prepared from the frontal cortex (1.8 mm anterior and 2.8 mm posterior to Bregma) to the hippocampus (2.3 mm posterior and 4.3 mm posterior to Bregma) and stained with hematoxylin-eosin (H&E). Sections were assessed for neuronal morphological changes with a Nikon light microscope equipped with a CCD Spot camera.

Neuronal marker, neuronal nuclei (NeuN), water channel membrane protein, aquaporin-4 (AQP-4), oxidative/nitrosative marker, 3-nitrotyrosine (3-NT), and vascular marker, endothelin 1 receptor A (ETRA), were analyzed to measure brain damage after exposure to BOP. Brain sections were incubated with mouse anti-NeuN (1 : 1000, Millipore), rabbit anti-AQP-4 (1 : 1000, Invitrogen), rabbit anti-nitrotyrosine (1 : 200, Millipore), and rabbit anti ETRA (1 : 500, Sigma) overnight at 4°C. After washes in PBS, the sections were incubated with the appropriate secondary antibodies labeled with Cy2 or Cy3 (1 : 500, Jackson ImmunoResearch) for 2 h at room temperature or overnight at 4°C. Slides were examined with a Nikon fluorescence microscope and images were captured with a CCD Spot camera.

2.5. Immunofluorescence Quantification

Images of six to eight sections were taken from each specified brain area per animal and were analyzed using Pro Image J Plus software. The average density of immunofluorescence of each animal was calculated based on the values of density in six to eight sections and was expressed as mean ± SEM. The statistical significance between groups was compared by ANOVA followed by Fisher LSD test for multiple comparisons.

3. Results

3.1. Histopathological Changes in Cortex and Hippocampus Exposed to BOP

H&E staining demonstrated some micropathological changes in frontal cortex and hippocampus one day after exposure to blast (Figures 1(a) and 1(b)). The pattern of brain damage corresponds with the detailed analysis of brain histopathology previously described in the same blast model [22].

3.2. Effect of Exposure to BOP on Neuronal Loss

In order to further examine the effect of BOP on neuropathological damage in cortex and hippocampus, immunoreactivity of mature neuronal marker, NeuN, was assessed after BOP exposure. NeuN-staining showed a significant decrease of immunoreactive neurons in cortex in both BOP groups by ~30% compared with controls (Figures 2(a) and 2(b)). In hippocampus, NeuN immunoreactivity in the CA1 region was reduced by 30% compared with nonexposed controls, with no significant differences between the two BOP exposed groups (Figures 2(c) and 2(d)). In the CA2 and CA3 regions of hippocampus, a significant decrease of NeuN immunoreactivity was observed only in one blast group (Blast) (Figures 2(c) and 2(d)). IJV compression attenuated the BOP-induced decrease of NeuN immunoreactivity in CA2/CA3 areas to a level not significantly different from controls (Figures 2(c) and 2(d)).

3.3. Effect of BOP on Brain Cytotoxic Edema

The upregulation of AQP-4, a water-channel protein, has been shown to facilitate cerebral cytotoxic edema formation in several TBI models [2224]. After exposure to BOP, AQP-4 expression was significantly increased in cortex of both BOP exposed groups compared with the control group (Figures 3(a) and 3(b)). In hippocampus, AQP-4 expression was increased after BOP across all areas, CA1 and CA2/CA3. IJV compression significantly eliminated or reduced this increase (Figures 3(c) and 3(d)).

3.4. Effect of BOP on Oxidative/Nitrosative Stress

Oxidative stress is known to play a role in the secondary injury mechanism following TBI [1012] and 3-NT is one of the markers of oxidative/nitrosative damage. Immunohistochemical quantification of 3-NT was performed to determine the extent of the oxidative mechanism activation after BOP in cortex and hippocampus. Over 50% increase in 3-NT immunoreactivity was observed in the cortex of the blast group (Blast). IJV compression (I-Blast) significantly attenuated this increase to a level that was not significantly different from the control group (Figures 4(a) and 4(b)). In hippocampus, BOP did not significantly activate 3-NT expression in CA1, CA2, and CA3 areas (Figures 4(c) and 4(d)).

3.5. Effect of BOP on ETRA

Cerebral vessels could be directly damaged by oxidants or by inflammation [25]. Endothelin 1 receptor A, ETRA, is localized in cerebral vessels and has been reported to be upregulated after TBI [2629]. The upregulation of ETRA is a component of cerebral microvessel alterations and vascular remodeling in TBI [27, 30]. In order to determine the vulnerability of cerebral vasculature to BOP, immunoreactivity of ETRA was assessed in brains of BOP exposed animals. The immunoreactivity of ETRA was significantly increased by over 50% in the cortex and hippocampus of the blast group. There was a nonsignificant difference between two blast exposed groups, Blast and I-Blast, in ETRA expression (Figures 5(a) and 5(b)).

4. Discussion

Several mechanisms of bTBI have been suggested; however, their relative contribution to brain damage remains unclear. These mechanisms include (1) direct interaction of the pressure wave with skull and subsequent transmission of energy through the brain, (2) transfer of kinetic energy from the blast wave through either the vascular system or cerebrospinal fluid, and (3) some indirect mechanism(s) caused by systemic factors and damage to other organs and tissues [31]. These proposed mechanisms are most likely not mutually exclusive and their contributions to brain damage can differ in various situations depending on intensity and spatial orientation to blast as well as on the presence of head and/or body protection.

The most effective protection would eliminate interaction between blast waves and brain with mechanical protective equipment, such as helmets and body shields. The emphasis on helmet technology has been only partially successful given the limitations of helmets to block acceleration-deceleration mechanisms which result in brain concussions [17]. In addition, helmets do not protect all skull areas and make them vulnerable to blast wave penetration. Recently, it was demonstrated that reduction in intracranial compliance by increased intracranial volume induced by IJV compression reduced brain injury caused by mechanical weight impact [18]. This effect is known as “slosh” and it is defined as the fluid dynamic forces that cause movement of the brain inside the cranium [32]. It has been suggested that mitigating “slosh” reduces differential motion and collision between brain and skull and ameliorates brain damage observed in a model of weight impact TBI [18]. The increases in the volume of fluid in the skull can be achieved by altering the volume of blood and CSF. Compression of brain venous outflow is the simplest way to increase brain fluid volume; as the inflow of arterial blood continues, the venous pressure increases along with an increase in ICP.

It is not known if the same mechanism of protection against cortical weight impact TBI by IJV compression can be as efficient against bTBI. TBI, as a result of mechanical impact on brain, is in large extent caused by acceleration-deceleration mechanisms with brain movements against the cranial wall and concussions being the predominant form of injury. During exposure to BOP, the primary damaging mechanism involves transfer of the shock wave energy through the skull and its interaction with brain tissue, while the damage by acceleration-deceleration mechanisms depends on the orientation to blast [33, 34]. More recent studies [8, 3538] have supported the theory that the pathophysiological mechanism of blast TBI also involves damage to the BBB and tiny cerebral blood vessels, which is caused by blood surging quickly through large blood vessels from the torso to the brain [39]. The direct mechanism of the primary bTBI also includes skull flexure [40, 41]. Results from numerical hydrodynamic simulations suggest that nonlethal blasts can induce sufficient skull flexure to generate potentially damaging loads in the brain, even without a head impact [40]. Skull flexure is also thought to be a contributing factor to the pressure wave measured inside the brain following exposure to BOP in both rats and swine depending on orientation to BOP, location of pressure probes, and skull thickness [4244].

In the current study, we assessed histopathological signs of blast-induced brain damage and the possible mitigating effect of IVP by immunofluorescence staining of specific markers of neuronal loss, brain edema, stress of oxidation/nitration, and vascular dysfunction. Immunofluorescence of neuronal marker NeuN was significantly decreased and expression of AQP-4 and ETRA was upregulated in both cortex and hippocampus consistent with neuronal loss, edema formation, and vascular dysfunction following exposure to BOP. The only exception was that 3-NT was increased in cortex but not in hippocampus. Consistent with these results, similar pathological changes induced by single or repeated exposure to 120 kPa BOP were previously reported [22, 45, 46]. These changes were seen as early as 3 h after blast and persisted for at least two days after BOP exposure. Furthermore, a selective vascular pathology and damage of BBB integrity were characteristic signs of bTBI [23, 47]. It has been suggested that a cascade of reactions initiated in the early phase after exposure to BOP, such as activation of oxidative mechanisms of damage, evolve into dysfunction of the BBB and damage to the vascular endothelium followed by impaired blood flow, neuronal apoptosis, and inflammatory damage to the brain [48]. The BOP-induced cellular pathology may be selective in different brain regions with different time courses of manifestation after blast exposure. This possibility was supported by the recent study demonstrating more extensive damage to the BBB integrity in hippocampus than in other brain regions [49]. On the other hand, more neuronal degeneration was observed in prefrontal cortex than in hippocampus at seven days after exposure to BOP [50].

It should be noted that our protocol minimized any contribution of acceleration-deceleration mechanism of damage by head movement, since the animal’s head was fixed to a solid holder and animals were exposed in the frontal, head-on position to the direction of BOP. Based on our results in the Blast group, it appears that, even with elimination of the head movement and acceleration-deceleration mechanisms, other mechanisms such as skull flexure and blood surge may still generate pressure gradient and brain damage after BOP.

The aim of this study was to determine if IJV compression, a maneuver designed to reduce cerebral compliance and increase ICP, can protect against blast-induced TBI. We did not instrument our animals to collect hemodynamic data. However, a study by Chou et al. [51] demonstrated that manual IJV compression in rats decreased venous return and increased ICP, while mean arterial pressure (MAP) decreased. The drop in MAP and increase in ICP may potentially result in reduced cerebral perfusion pressure (CPP) that is defined as a difference between MAP and ICP. During 1 minute of manual jugular vein compression, the ICP increased from 6.9 to 9.2 mmHg and MAP decreased from 97 to 90 mmHg, resulting in a calculated CPP decrease from 90 mmHg to 81 mmHg during the test. This value remains above the critical CPP at which cerebral blood flow begins to fall (50 mmHg). Within 30 s after release of compression, both ICP and MAP returned to their control values. Based on their results, it appears that IJV compression for 1 min does not result in the CPP falling below the critical level.

The protective effect of IJV compression was evaluated in frontal cortex and hippocampus as areas predominantly involved in cognition, learning and memory, and emotional functions that are related to behavioral impairment after BOP [46, 5254]. Our data indicate that IJV compression reduced selective pathological changes after exposure to BOP. IJV compression appeared to be more effective in attenuating the NeuN decrease and the upregulation of AQP-4 in hippocampus as compared to the cortex, suggesting a selective effect of IJV compression. On the other hand, the extent of oxidative and nitrosative damage as determined by 3-NT immunoreactivity was higher in cortex and IJV significantly prevented the 3-NT increase. ETRA fluorescence was elevated in both the cortex and the hippocampus after BOP and remained elevated after IJV compression around 25% over control. Our results show that the decrease in brain compliance by increase in ICP can alleviate brain damage not only in the blunt trauma induced TBI but also in bTBI, in this case likely by mitigating the contribution of skull flexure to the interaction of brain with the cranium.

Plastic neck collars have already been developed to mildly compress the jugular vein bilaterally to increase intracranial blood volume [55]. The collar was worn by hockey players at each practice session and game over the entire hockey season to prevent brain concussions by mechanical impact. The collar device did not cause any structural brain damage or change in cerebral metabolism as evidenced by MR imaging and EEG recording. It was found that the group of players that wore the collars had reduced alterations in white matter compared with the noncollar group.

In conclusion, the present study indicates that IJV compression has a protective potential in bTBI by attenuating blast-induced neurodegeneration, edema, oxidative damage, and vascular dysfunction. Although further studies are needed to explore the mechanism(s) mediated by slosh mitigation and its potential clinical application, our findings suggest that IJV compression has significant promise as a protective measure against bTBI.

Ethical Approval

The study protocol was reviewed and approved by the Walter Reed Army Institute of Research/Naval Medical Research Center Institutional Animal Care and Use Committee in accordance with the principles set forth in the “Guide for the Care and Use of Laboratory Animals” by Institute of Laboratory Animal Resources, National Research Council, National Academy Press, 1996.

Disclosure

The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Department of Navy, Department of Defense, or the US Government. Richard McCarron is a military service member (or employee of the US Government). This work was prepared as part of his official duties. Title 17 U.S.C. §105 provides that “copyright protection under this title is not available for any work of the United States Government.” Title 17 U.S.C. §101 defines a US Government work as a work prepared by military service men or employee of the US Government as part of that person’s official duties.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was supported by Office of Naval Research (ONR) Work Unit (601152N.0000.000.A1308).

References

  1. B. D. Owens, J. F. Kragh Jr., J. C. Wenke, J. Macaitis, C. E. Wade, and J. B. Holcomb, “Combat wounds in operation iraqi freedom and operation enduring freedom,” Journal of Trauma, vol. 64, no. 2, pp. 295–299, 2008. View at: Publisher Site | Google Scholar
  2. S. B. Shively and D. P. Perl, “Traumatic brain injury, shell shock, and posttraumatic stress disorder in the military—past, present, and future,” Journal of Head Trauma Rehabilitation, vol. 27, no. 3, pp. 234–239, 2012. View at: Publisher Site | Google Scholar
  3. S. Okie, “Traumatic brain injury in the war zone,” The New England Journal of Medicine, vol. 352, no. 20, pp. 2043–2047, 2005. View at: Publisher Site | Google Scholar
  4. M. Chavko, T. Watanabe, S. Adeeb, J. Lankasky, S. T. Ahlers, and R. M. McCarron, “Relationship between orientation to a blast and pressure wave propagation inside the rat brain,” Journal of Neuroscience Methods, vol. 195, no. 1, pp. 61–66, 2011. View at: Publisher Site | Google Scholar
  5. I. Cernak, Z. Wang, J. Jiang, X. Bian, and J. Savic, “Ultrastructural and functional characteristics of blast injury-induced neurotrauma,” Journal of Trauma, vol. 50, no. 4, pp. 695–706, 2001. View at: Publisher Site | Google Scholar
  6. C. R. Bass, M. B. Panzer, K. A. Rafaels, G. Wood, J. Shridharani, and B. Capehart, “Brain injuries from blast,” Annals of Biomedical Engineering, vol. 40, no. 1, pp. 185–202, 2012. View at: Publisher Site | Google Scholar
  7. R. K. Gupta and P. A. Przekwas, “Mathematical models of blast-induced TBI: current status, challenges, and prospects,” Frontiers in Neurology, vol. 30, no. 4, pp. 59–80, 2013. View at: Google Scholar
  8. C. D. Hue, S. Cao, S. F. Haider et al., “Blood-brain barrier dysfunction after primary blast injury in vitro,” Journal of Neurotrauma, vol. 30, no. 19, pp. 1652–1663, 2013. View at: Publisher Site | Google Scholar
  9. R. D. Readnower, M. Chavko, S. Adeeb et al., “Increase in blood-brain barrier permeability, oxidative stress, and activated microglia in a rat model of blast-induced traumatic brain injury,” Journal of Neuroscience Research, vol. 88, no. 16, pp. 3530–3539, 2010. View at: Publisher Site | Google Scholar
  10. B. Uttara, A. V. Singh, P. Zamboni, and R. T. Mahajan, “Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options,” Current Neuropharmacology, vol. 7, no. 1, pp. 65–74, 2009. View at: Publisher Site | Google Scholar
  11. Y. Zhang, Y. Yang, H. Tang et al., “Hyperbaric oxygen therapy ameliorates local brain metabolism, brain edema and inflammatory response in a blast-induced traumatic brain injury model in rabbits,” Neurochemical Research, vol. 39, no. 5, pp. 950–960, 2014. View at: Publisher Site | Google Scholar
  12. B. P. Lucke-Wold, Z. J. Naser, A. F. Logsdon et al., “Amelioration of nicotinamide adenine dinucleotide phosphate-oxidase mediated stress reduces cell death after blast-induced traumatic brain injury,” Translational Research, vol. 166, no. 6, pp. 509.e1–528.e1, 2015. View at: Publisher Site | Google Scholar
  13. S. L. Bratton, R. M. Chestnut, J. Ghajar et al., “Guidelines for the management of severe traumatic brain injury. VIII. Intracranial pressure thresholds,” Journal of Neurotrauma, vol. 24, supplement 1, pp. S55–S58, 2007. View at: Publisher Site | Google Scholar
  14. K. W. McConeghy, J. Hatton, L. Hughes, and A. M. Cook, “A review of neuroprotection pharmacology and therapies in patients with acute traumatic brain injury,” CNS Drugs, vol. 26, no. 7, pp. 613–636, 2012. View at: Publisher Site | Google Scholar
  15. M. E. Carey, M. Herz, B. Corner et al., “Ballistic helmets and aspects of their design,” Neurosurgery, vol. 47, no. 3, pp. 678–689, 2000. View at: Google Scholar
  16. K. C. Curley, M. Leggieri, and M. S. Jaffee, “Opening editorial, international state of the science meeting on non-impact blast-induced mild traumatic brain injury,” NeuroImage, vol. 54, pp. S14–S20, 2011. View at: Publisher Site | Google Scholar
  17. R. C. Turner, Z. J. Naser, J. E. Bailes, D. W. Smith, J. A. Fisher, and C. L. Rosen, “Effect of slosh mitigation on histologic markers of traumatic brain injury: laboratory investigation,” Journal of Neurosurgery, vol. 117, no. 6, pp. 1110–1118, 2012. View at: Publisher Site | Google Scholar
  18. D. W. Smith, J. E. Bailes, J. A. Fisher, J. Robles, R. C. Turner, and J. D. Mills, “Internal jugular vein compression mitigates traumatic axonal injury in a rat model by reducing the intracranial slosh effect,” Neurosurgery, vol. 70, no. 3, pp. 740–746, 2012. View at: Publisher Site | Google Scholar
  19. J. C. Chapman and R. Diaz-Arrastia, “Military traumatic brain injury: a review,” Alzheimer's and Dementia, vol. 10, no. 3, pp. S97–S104, 2014. View at: Publisher Site | Google Scholar
  20. D. M. Gullotti, M. Beamer, M. B. Panzer et al., “Significant head accelerations can influence immediate neurological impairments in a murine model of blast-induced traumatic brain injury,” Journal of Biomechanical Engineering, vol. 136, no. 9, pp. 1004–1015, 2014. View at: Publisher Site | Google Scholar
  21. M. Chavko, W. K. Prusaczyk, and R. M. McCarron, “Protection against blast-induced mortality in rats by hemin,” The Journal of Trauma, vol. 65, no. 5, pp. 1140–1145, 2008. View at: Publisher Site | Google Scholar
  22. J. J. Dalle Lucca, M. Chavko, M. A. Dubick et al., “Blast-induced moderate neurotrauma (BINT) elicits early complement activation and tumor necrosis factor alpha (TNFα) release in a rat brain,” Journal of the Neurological Sciences, vol. 318, no. 1-2, pp. 146–154, 2012. View at: Publisher Site | Google Scholar
  23. P. M. Abdul-Muneer, H. Schuetz, F. Wang et al., “Induction of oxidative and nitrosative damage leads to cerebrovascular inflammation in an animal model of mild traumatic brain injury induced by primary blast,” Free Radical Biology and Medicine, vol. 60, pp. 282–291, 2013. View at: Publisher Site | Google Scholar
  24. S. Saadoun and M. C. Papadopoulos, “Aquaporin-4 in brain and spinal cord oedema,” Neuroscience, vol. 168, no. 4, pp. 1036–1046, 2010. View at: Publisher Site | Google Scholar
  25. M. M. Bachschmid, S. Schildknecht, R. Matsui et al., “Vascular aging: chronic oxidative stress and impairment of redox signaling—consequences for vascular homeostasis and disease,” Annals of Medicine, vol. 45, no. 1, pp. 17–36, 2013. View at: Publisher Site | Google Scholar
  26. W. M. Armstead and C. W. Kreipke, “Endothelin-1 is upregulated after traumatic brain injury: a cross-species, cross-model analysis,” Neurological Research, vol. 33, no. 2, pp. 133–136, 2011. View at: Publisher Site | Google Scholar
  27. T. Petrov and J. A. Rafols, “Acute alterations of endothelin-1 and iNOS expression and control of the brain microcirculation after head trauma,” Neurological Research, vol. 23, no. 2-3, pp. 139–143, 2001. View at: Publisher Site | Google Scholar
  28. J. Steiner, D. Rafols, H. K. Park, M. S. Katar, J. A. Rafols, and T. Petrov, “Attenuation of iNOS mRNA exacerbates hypoperfusion and upregulates endothelin-1 expression in hippocampus and cortex after brain trauma,” Nitric Oxide, vol. 10, no. 3, pp. 162–169, 2004. View at: Publisher Site | Google Scholar
  29. S. Kallakuri, C. W. Kreipke, P. C. Schafer, S. M. Schafer, and J. A. Rafols, “Brain cellular localization of endothelin receptors A and B in a rodent model of diffuse traumatic brain injury,” Neuroscience, vol. 168, no. 3, pp. 820–830, 2010. View at: Publisher Site | Google Scholar
  30. J. A. Rafols, C. W. Kreipke, and T. Petrov, “Alterations in cerebral cortex microvessels and the microcirculation in a rat model of traumatic brain injury: a correlative EM and laser Doppler flowmetry study,” Neurological Research, vol. 29, no. 4, pp. 339–347, 2007. View at: Publisher Site | Google Scholar
  31. I. Cernak and L. J. Noble-Haeusslein, “Traumatic brain injury: an overview of pathobiology with emphasis on military populations,” Journal of Cerebral Blood Flow and Metabolism, vol. 30, no. 2, pp. 255–266, 2010. View at: Publisher Site | Google Scholar
  32. R. A. Ibrahim, V. N. Pilipchuk, and T. Ikeda, “Recent advances in liquid sloshing dynamics,” Applied Mechanics Reviews, vol. 54, no. 2, pp. 133–199, 2001. View at: Publisher Site | Google Scholar
  33. P. A. Taylor and C. C. Ford, “Simulation of blast-induced early-time intracranial wave physics leading to traumatic brain injury,” Journal of Biomechanical Engineering, vol. 131, no. 6, 2009. View at: Publisher Site | Google Scholar
  34. M. K. Nyein, A. M. Jason, L. Yu et al., “In silico investigation of intracranial blast mitigation with relevance to military traumatic brain injury,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 48, pp. 20703–20708, 2010. View at: Publisher Site | Google Scholar
  35. S. Assari, K. Laksari, M. Barbe, and K. Darvish, “Cerebral blood pressure rise during blast exposure in a rat model of blast-induced traumatic brain injury,” in Proceedings of the 9th Annual Injury Biomechanics Symposium, Columbus, Ohio, USA, May 2013. View at: Google Scholar
  36. Y. Chen, W. Huang, and S. Constantini, “Blast shock wave mitigation using the hydraulic energy redirection and release technology,” PLoS ONE, vol. 7, no. 6, Article ID e39353, 2012. View at: Publisher Site | Google Scholar
  37. M. A. G. Sosa, R. De Gasperi, A. J. Paulino et al., “Blast overpressure induces shear-related injuries in the brain of rats exposed to a mild traumatic brain injury,” Acta Neuropathologica Communications, vol. 1, article 51, pp. 1–15, 2013. View at: Publisher Site | Google Scholar
  38. S. Yeoh, E. D. Bell, and K. L. Monson, “Distribution of blood-brain barrier disruption in primary blast injury,” Annals of Biomedical Engineering, vol. 41, no. 10, pp. 2206–2214, 2013. View at: Publisher Site | Google Scholar
  39. Y. Chen and W. Huang, “Non-impact, blast-induced mild TBI and PTSD: concepts and caveats,” Brain Injury, vol. 25, no. 7-8, pp. 641–650, 2011. View at: Publisher Site | Google Scholar
  40. W. C. Moss, M. J. King, and E. G. Blackman, “Skull flexure from blast waves: a mechanism for brain injury with implications for helmet design,” Physical Review Letters, vol. 103, no. 10, Article ID 108702, 2009. View at: Publisher Site | Google Scholar
  41. A. Dal Cengio Leonardi, N. J. Keane, K. Hay, A. G. Ryan, C. A. Bir, and P. J. Vandevord, “Methodology and evaluation of intracranial pressure response in rats exposed to complex shock waves,” Annals of Biomedical Engineering, vol. 41, no. 12, pp. 2488–2500, 2013. View at: Publisher Site | Google Scholar
  42. R. A. Bauman, G. Ling, L. Tong et al., “An introductory characterization of a combat-casualty-care relevant swine model of closed head injury resulting from exposure to explosive blast,” Journal of Neurotrauma, vol. 26, no. 6, pp. 841–860, 2009. View at: Publisher Site | Google Scholar
  43. K. Feng, L. Zhang, X. Jin et al., “Biomechanical responses of the brain in swine subject to free-field blasts,” Frontiers in Neurology, vol. 7, pp. 179–191, 2016. View at: Publisher Site | Google Scholar
  44. R. Bolander, B. Mathie, C. Bir, D. Ritzel, and P. Vandevord, “Skull flexure as a contributing factor in the mechanism of injury in the rat when exposed to a shock wave,” Annals of Biomedical Engineering, vol. 39, no. 10, pp. 2550–2559, 2011. View at: Publisher Site | Google Scholar
  45. H. J. Cho, V. S. S. S. Sajja, P. J. VandeVord, and Y. W. Lee, “Blast induces oxidative stress, inflammation, neuronal loss and subsequent short-term memory impairment in rats,” Neuroscience, vol. 253, no. 3, pp. 9–20, 2013. View at: Publisher Site | Google Scholar
  46. A. Kamnaksh, S.-K. Kwon, E. Kovesdi et al., “Neurobehavioral, cellular, and molecular consequences of single and multiple mild blast exposure,” Electrophoresis, vol. 33, no. 24, pp. 3680–3692, 2012. View at: Publisher Site | Google Scholar
  47. M. A. Gama Sosa, R. De Gasperi, P. L. Janssen et al., “Selective vulnerability of the cerebral vasculature to blast injury in a rat model of mild traumatic brain injury,” Acta Neuropathologica Communications, vol. 2, article 67, 2014. View at: Publisher Site | Google Scholar
  48. M. Vuceljić, G. Zunić, P. Romić, and M. Jevtić, “Relation between both oxidative and metabolic-osmotic cell damages and initial injury severity in bombing casualties,” Vojnosanitetski Pregled, vol. 63, no. 6, pp. 545–551, 2006. View at: Publisher Site | Google Scholar
  49. S. Kabu, H. Jaffer, M. Petro et al., “Blast-associated shock waves result in increased brain vascular leakage and elevated ROS levels in a rat model of traumatic brain injury,” PLoS ONE, vol. 10, no. 5, Article ID e0127971, 2015. View at: Publisher Site | Google Scholar
  50. V. S. S. S. Sajja, W. B. Hubbard, C. S. Hall, F. Ghoddoussi, M. P. Galloway, and P. J. VandeVord, “Enduring deficits in memory and neuronal pathology after blast-induced traumatic brain injury,” Scientific Reports, vol. 5, Article ID 15075, 2015. View at: Publisher Site | Google Scholar
  51. C.-H. Chou, M.-L. Doong, J.-L. Fuh, J.-C. Wu, and S.-J. Wang, “Queckenstedt's test affects more than jugular venous congestion in rat,” PLoS ONE, vol. 8, no. 3, Article ID e59409, 6 pages, 2013. View at: Publisher Site | Google Scholar
  52. G. A. Elder and A. Cristian, “Blast-related mild traumatic brain injury: mechanisms of injury and impact on clinical care,” Mount Sinai Journal of Medicine, vol. 76, no. 2, pp. 111–118, 2009. View at: Publisher Site | Google Scholar
  53. J. D. Kocsis and A. Tessler, “Pathology of blast-related brain injury,” Journal of Rehabilitation Research and Development, vol. 46, no. 6, pp. 667–672, 2009. View at: Publisher Site | Google Scholar
  54. S.-K. C. Kwon, E. Kovesdi, A. B. Gyorgy et al., “Stress and traumatic brain injury: a behavioral, proteomics, and histological study,” Frontiers in Neurology, vol. 2, no. 12, pp. 1–14, 2011. View at: Publisher Site | Google Scholar
  55. G. D. Myer, W. Yuan, K. D. Barber Foss et al., “The effects of external jugular compression applied during head impact exposure on longitudinal changes in brain neuroanatomical and neurophysiological biomarkers: a preliminary investigation,” Frontiers in Neurology, vol. 7, article 74, 2016. View at: Publisher Site | Google Scholar

Copyright © 2017 Ming Gu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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