Systemic Inflammatory Effects of Traumatic Brain Injury, Femur Fracture, and Shock: An Experimental Murine Polytrauma Model

Probst, C.; Mirzayan, M. J.; Mommsen, P.; Zeckey, C.; Tegeder, T.; Geerken, L.; Maegele, M.; Samii, A.; van Griensven, M.

doi:https://doi.org/10.1155/2012/136020

Mediators of Inflammation

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Posttraumatic Immune Response and Its Modulation

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Research Article | Open Access

Volume 2012 | Article ID 136020 | https://doi.org/10.1155/2012/136020

Systemic Inflammatory Effects of Traumatic Brain Injury, Femur Fracture, and Shock: An Experimental Murine Polytrauma Model

C. Probst,¹M. J. Mirzayan,²P. Mommsen,³C. Zeckey,³T. Tegeder,³L. Geerken,⁴M. Maegele,¹A. Samii,⁵and M. van Griensven⁶

Academic Editor: Frank Hildebrand

Received13 Oct 2011

Accepted06 Dec 2011

Published04 Mar 2012

Abstract

Objective. Despite broad research in neurotrauma and shock, little is known on systemic inflammatory effects of the clinically most relevant combined polytrauma. Experimental investigation in an animal model may provide relevant insight for therapeutic strategies. We describe the effects of a combined injury with respect to lymphocyte population and cytokine activation. Methods. 45 male C57BL/6J mice (mean weight 27 g) were anesthetized with ketamine/xylazine. Animals were subjected to a weight drop closed traumatic brain injury (WD-TBI), a femoral fracture and hemorrhagic shock (FX-SH). Animals were subdivided into WD-TBI, FX-SH and combined trauma (CO-TX) groups. Subjects were sacrificed at 96 h. Blood was analysed for cytokines and by flow cytometry for lymphocyte populations. Results. Mortality was 8%, 13% and 47% for FX-SH, WD-TBI and CO-TX groups (). TNFα (11/13/139 for FX-SH/WD-TBI/CO-TX; ), CCL2 (78/96/227; ) and IL-6 (16/48/281; ) showed significant increases in the CO-TX group. Lymphocyte populations results for FX-SH, WD-TBI and CO-TX were: CD-4 (31/21/22; n.s.), CD-8 (7/28/34, ), CD-4-CD-8 (11/12/18; n.s.), CD-56 (36/7/8; ). Conclusion. This study shows that a combination of closed TBI and femur-fracture/ shock results in an increase of the humoral inflammation. More attention to combined injury models in inflammation research is indicated.

1. Introduction

Trauma and especially multiple trauma including traumatic brain injury (TBI) are the most common killers in children and adults before age 50 around the world [1–3]. Mortality of multiple trauma including TBI following traffic accidents ranges between 18% and 25% [1, 4]. But not only the first hours and days are critical; for years, more and more multiple trauma patients have been surviving the initial accident and acute care period but only to develop systemic inflammatory response syndrome (SIRS), sepsis, or multiple organ dysfunction syndrome (MODS) in the course of the few weeks of critical care [2, 5, 6].

For 5000 multiple trauma patients in Germany, the German Trauma Registry showed an in-hospital mortality of 12% in 2010. In the same report, critical care complications such as SIRS, sepsis, and MODS are reported for 15% of patients. Other groups report similar rates of SIRS, sepsis, and MODS [2, 6, 7]. It is generally known that these complications again deteriorate the prognosis and outcome of the initially surviving trauma patient and increase late mortality to up to 50% if manifest MODS is developed [2, 7, 8].

To understand pathophysiological processes leading to multiple organ failure, SIRS, and sepsis and taking place during this devastating illness, profound pathophysiological knowledge on the effects of the initial trauma (“first hit”) is essential to minimize additional harm by the following surgical or critical care treatment (potential “second hit”) [9–11].

Therefore, numerous neurotrauma as well as shock research studies with many different animal and clinical models showed inflammatory changes after trauma [12–14]. Only recently, Semple et al. reported on the important role of CCL2 in C57Bl/J6 mice, peaking at 4 to 12 h following closed head injury and leading to improved functional outcome and lesion size reduction as well as less secondary brain damage [15]. Another group showed that the substance Minozac may attenuate the effect of proinflammatory cytokines after closed TBI in mice. In the same study, the authors discussed if Minozac may also increase long-term neurofunction after TBI [16]. On the other hand, femur fracture and shock in mice are known to trigger an inflammatory response for years, and recently several groups discussed therapeutic strategies to modulate this inflammatory response [12, 14].

However, little attention has been paid to the immune reaction following combined trauma and the interaction of the brain and the other organs of the body. This is even more important, since the injury pattern of closed TBI, lower extremity fracture, and shock is very common in multiply injured patients treated in trauma centers around the world. Therefore, we investigated the humoral and cellular inflammatory changes of the combined TBI, shock, and femur fracture in a polytrauma model of the mouse.

2. Material and Methods

2.1. Animal Care

The study was approved by the Animal Research Committee of the Hannover Medical School (Medizinische Hochschule Hannover, MHH) and the county government of Lower Saxony (Bezirksregierung Niedersachsen), no. 03/672.

45 male C57BL/J6 mice aged 8–10 weeks with a mean weight of 27.4 g (±3.7 g) were used for the study. The animals were bred and raised in the central animal facility of our institution. All animals were handled at room temperature for 7 days before treatment. Throughout the study period, pelleted mouse feed (Altromin 1324) and water were available ad libitum. The lighting was maintained on a 12-hour cycle. Room temperature was maintained at a constant 20° ± 2°C.

2.2. Anesthesia

Analgetic therapy during the whole time of the study was provided by Metamizol 25 mg/1000 mL (Novaminsulfon ratiopharm, Ratiopharm GmbH, Ulm) in the drinking water of the animals ad libitum.

All surgical and trauma procedures were performed at a level of deep surgical anesthesia during maintained spontaneous breathing. For anesthesia, subcutaneous injection of Ketamine (Ketanest, Parke-Davis GmbH, Karlsruhe, Germany) with a dose of 100 mg/kg body weight and 2% Xylazine (Rompun, Bayer Vital GmbH, Leverkusen, Germany) with a dose of 16 mg/kg body weight were used. The eyes of the animals were covered by Dexpanthenol (Bepanthen, Hoffmann-La Roche AG, Grenzach-Wyhlen, Switzerland). The trauma and perioperative care was performed under an infrared heating lamp. Thereby body temperature of 36°C could be maintained.

2.3. Weight Drop Traumatic Brain Injury (WD-TBI)

30 of the animals underwent a standard WD-TBI following a model published previously by Shapira et al. [17] with modification according to Chen et al. [18]. Under a surgical level of anesthesia, the animal was positioned in a stereotaxic frame, the head was shaved, and the exposed scalp disinfected by Softasept N (Braun, Melsungen, Germany). A midline incision was performed, and the skull was exposed. Next, the 3 mm diameter probe was positioned on the planned impact point at the left of the sagittal suture and caudad to the coronal suture. The trauma was now performed with a mean velocity of 3 m/s by a software-guided process (“Labview,” National Instruments, Austin, TX, USA).

Animals were taken out from the stereotaxic frame while still anesthetized. The wound was irrigated and closed by 4.0 prolene sutures. (Ethicon, Norderstedt, Germany). Afterwards, the animals remained under continuous observation and warming until full recovery was reached.

2.4. Femur Fracture

Femur fracture was applied by a blunt guillotine device according to Van Griensven et al. [19], We used a weight of 400 g falling out of a height of 160 mm on the fixed femur. Success of the fracture mechanism was controlled clinically (crepitation and instability), while the animal was still in anesthesia. If both of the clinical signs were absent, the trauma was repeated. The repeated procedure was required in one animal only. The guillotine procedure resulted in an A-type femur fracture combined with a moderate soft tissue injury. After completion of the injury, we performed a closed reduction and splinting of the fracture by a piece of wood in proper length that was tied to the fractured extremity proximally and distally of the fracture.

2.5. Shock

After both traumata were set, we draw 60% of the blood volume of the respective mouse via an orbital puncture with a heparinized capillary. Volume was restored after 1 hour of shock with Ringer’s solution four times the extracted blood volume into the tail vein. This resulted in an individual resuscitation procedure. Only after this resuscitation was completed and the animal showed 36°C of body temperature, anesthesia was terminated and the animal awoke [19].

2.6. Analysis of the Cytokines and Lymphocytes

Subjects were sacrificed 96 hours after trauma by exsanguination in deep surgical anaesthesia, while blood samples for cytokines were extracted. As well the spleen was harvested, and a suspension was produced. This suspension was used for lymphocyte analysis as described earlier [19]. Lymphocytes were analyzed using standard flow cytometry (FACS analysis) for CD-4, CD-8, CD-4-CD-8, and CD-56 cells (FACS Calibur, BD Biosciences, Heidelberg, Germany). The procedures have been described earlier [19].

Serum cytokines (tumor necrosis factor α, TNFα; chemokine CC2 ligand, CCL2; interleukins 6 and 12, IL-6 and IL-12) were analyzed by cytometric bead array technique (BDTM Cytometric Bead Array Mouse Inflammation Kit, BD Biosciences, Pharmingen, Germany) and FACS as described earlier [19].

2.7. Statistics

Analysis of continuous parameters was by ANOVA and a post hoc Tukey test. Mortality ratios were analyzed by chi-squared test. Results are reported as mean ± standard error of the mean (SEM). For statistical analysis, SPSS 14.0 software was used. Statistical significance was set at .

3. Results

3.1. Mortality

The polytraumatized animals showed a significantly higher mortality than the animals of both singular trauma groups (Figure 1). There was no immediate death. Deaths occurred between 24 and 72 hours after trauma.

3.2. Humoral Inflammatory Markers

TNFα, CCL2, and IL-6 showed significantly higher concentrations at 96 h after trauma in the CO-TX group, while the single-trauma groups seem to raise their cytokine levels clearly less and without significant differences between groups WD-TBI and FX-SH (Figure 2). IL-12 showed no difference in plasma concentration between the groups at 96 h after trauma.

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3.3. Lymphocyte Populations

The CD-8 ratio was significantly lower, and the CD-56 ratio was significantly higher in the FX-SH mice than in each of the other groups. CD-4 and CD-4-CD-8 ratios showed no difference between groups (Figure 3).

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4. Discussion

While the intracranial effects of traumatic brain injury have been a subject of multiple studies, the aim of this study was to investigate the interaction of the brain injury and systemic shock after lower extremity trauma in regard to changes in the inflammatory response.

Our main results were:(1)increased levels of TNFα, CCL2, and IL-6 in the CO-TX group,(2)lower rates of CD-8 and higher rates of CD-56 cells in the FX-SH group,(3)an increased mortality in the combined trauma animal group.

However, some weaknesses of our study have to be kept in mind. As always in animal studies, the findings cannot completely be extrapolated to human pathophysiology and clinical treatment strategies. Nonetheless, mouse models are very common due to their availability, ease of handling, and practicability. Anyhow, a correlation with similar large animal models and additional studies in humans are required to complete our findings and value the clinical relevance. Furthermore, the injury pattern may seem artificial in its constellation since one huge challenge of human polytrauma studies is the diversity of injury patters requiring complex inclusion and exclusion procedures to gain comparable populations in terms of injury severity and injury pattern. However, in our point of view, this strengthens our study: the injury pattern and severity of our individuals is highly standardized, and the model and both its components are robust and reproducible. So comparability of our injuries and populations is granted, even more so with regard to the complex hypothesis of a combined trauma being more than only the sum of its parts. This holds even true for standard parameters such as weight, size, sex, and age, that usually also affect human studies of polytrauma patients.

Our first finding supports any injury severity-related changes in inflammatory response reported from humans [2, 20–22]. Our CO-TX group simply suffered more severe injuries than the FX-SH and WD-TBI groups. Looking at each monotrauma, our plasma cytokine levels are comparable to those reported earlier in literature [12, 14]. However, the levels of the proinflammatory cytokines are elevated not only by factor 2 but by factors 3 to 10, respectively, even as late as 96 hours after trauma. Other groups found similar results: TNFα was associated with injury severity earlier. Likewise, in a murine trauma-haemorrhage model, other authors reported TNFα elevations [23, 24]. The same holds true for TBI in humans [25, 26] and clinically relevant models of TBI [27]. While these groups reported elevated TNFα levels 1 to 4 h after trauma, later publications also found TNFα effects on neuronal recovery and prevention of secondary brain damage [28]. One group reported elevated plasma TNFα levels after TBI. So, while the importance of TNFα after peripheral or brain injury remains rather clear and reciprocal effects were described to some extent, we found no earlier report on the extent of TNFα plasma level rise after combined TBI and trauma haemorrhage. Concerning IL-6, Maegele et al. reported a 3-4 fold increase in circulating plasma levels after combined fracture and fluid percussion TBI in rats [29]. In humans, IL-6 was classified as the most important secondary cytokine in trauma [30], not only because of its multitude of mainly proinflammatory effects and its association to the severity of trauma, but also because of its prognostic relevance differing survivors and nonsurvivors. So, highest IL-6 levels in the most severe trauma group and the highest mortality are in line with earlier results in literature. However, the magnitude of the increase was rarely described. Similarly, CCL-2 is increased in the brain after TBI and leads to increased migration of intravascular leukocytes across a damaged blood-brain barrier [31, 32]. As well CCL-2 was found to play a key role in the development of organ dysfunction after trauma by activating monocytes/macrophages to migrate from the intravascular space into peripheral tissues. While Thibeault et al. showed no association between IL-6 and CCL-2 after trauma, they could show such an association between TNFα and CCL-2 [33]. So, while being in line with recent literature, our findings also remain conclusive within themselves with respect to the inflammatory cascades described earlier. With respect to proinflammatory IL-12, our nonsignificantly low serum levels are backed up by recent literature. In TBI, one author described differences in IL-12 after 24 h but not later [30]. In human multiple trauma patients suffering from chest trauma, IL-12 was reported to inversely correlate with mortality [30]. Furthermore, IL-12 seems to exert some major effects via CD56+-(NK-) cells [30]. However, depressed IL-12 production in trauma patients was associated with a shift towards a CD4+(TH2) type pattern of adverse clinical outcome [30].

While numerous reports focus on intravascular lymphocyte populations and function after trauma, the populations crucial for MODS to develop are those in peripheral tissues [30]. The significant decrease of the CD-8+ ratio in the splenic suspension of our FX-SH group is supported by the earlier finding of a decreased ratio of CD-8+ lymphocytes in peripheral tissues after trauma hemorrhage compared to controls [34]. However, we found no report on lymphocyte populations in peripheral tissues after traumatic brain injury. Yet, the WD-TBI group might be comparable to controls for peripheral trauma and hemorrhage (our FX-SH group) and therefore shows higher CD-8+ ratios. Still, this hypothesis does not explain the CD-8+ ratio of the CO-TX group. Restoration of the low CD-8+ ratio after FX-SH by WD-TBI might be speculated on but so far no theory on responsible mechanisms is known. Since this result was rather surprising for our group, detailed evaluation of key processes for lymphocyte populations after combined neuro- and peripheral trauma and hemorrhage must be left for future experiments. CD-56-(NK-) cells were found in a significantly higher concentration in the splenic suspension of our FX-SH group compared to our WD-TBI and CO-TX groups. This also is supported by earlier results as in CD-8+ cells [34]. While the same reasons as above for the physiologic CD-56 ratio in our WD-TBI group may be discussed, in the CO-TX group one more aspect needs consideration: raised TNFα levels in a murine sepsis model were associated with an increased ratio of NK cells [35, 36]. However, for CD-56+ cells as well as for CD-8+ cells, the detailed mechanisms and reasons underlying the differences found in our study cannot readily be explained. Further experiments should focus on lymphocyte populations in peripheral tissues after TBI and combined TBI and trauma hemorrhage.

Mortality may just reflect the inflammatory changes and/or trauma load [1, 12]. In humans, injury severity clearly is associated with mortality. Likewise, injury severity was associated with an increased inflammatory response as measured by increased IL-6 levels. So was mortality, an increased IL-6 level in multiply injured patients was associated with increased mortality. IL-6 even was suggested to be used for prognosis in severe trauma [2, 30]. In murine models, other groups support the findings in humans and of our study [12, 14, 37].

5. Conclusion

Our animal model of combined extremity fracture, shock, and closed traumatic brain injury clearly showed that the inflammatory response of the combined trauma is severalfold elevated as compared to the respective monotrauma in terms of humoral parameters. The almost physiological findings for peripheral tissue lymphocyte populations in the isolated TBI and in the combined trauma group as compared to the significantly elevated ratios of the trauma-hemorrhage group are not readily explained and need further evaluation. Mortality in our combined trauma model is clearly associated with trauma load and inflammation and such parallels the findings in multiple trauma patients. This shows the value of our model for future investigations.

Authors’ Contribution

C. Probst and M. J. Mirzayan contributed equally to this study.

References

C. J. L. Murray and A. D. Lopez, “Alternative projections of mortality and disability by cause 1990–2020: Global Burden of Disease Study,” Lancet, vol. 349, no. 9064, pp. 1498–1504, 1997.
View at: Publisher Site | Google Scholar
M. Frink, M. van Griensven, P. Kobbe et al., “IL-6 predicts organ dysfunction and mortality in patients with multiple injuries,” Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, vol. 17, p. 49, 2009.
View at: Google Scholar
C. Probst, B. A. Zelle, N. A. Sittaro, R. Lohse, C. Krettek, and H. C. Pape, “Late death after multiple severe trauma: when does it occur and what are the causes?” The Journal of Trauma, vol. 66, no. 4, pp. 1212–1217, 2009.
View at: Google Scholar
M. Bardenheuer, U. Obertacke, C. Waydhas, and D. Nast-Kolb, “Epidemiology of the severe multiple trauma—a prospective registration of preclinical and clinical supply,” Unfallchirurg, vol. 103, no. 5, pp. 355–363, 2000.
View at: Publisher Site | Google Scholar
D. Nast-Kolb, M. Aufmkolk, S. Rucholtz, U. Obertacke, and C. Waydhas, “Multiple organ failure still a major cause of morbidity but not mortality in blunt multiple trauma,” Journal of Trauma, vol. 51, no. 5, pp. 835–842, 2001.
View at: Google Scholar
G. Regel, M. Grotz, T. Weltner, J. A. Sturm, and H. Tscherne, “Pattern of organ failure following severe trauma,” World Journal of Surgery, vol. 20, no. 4, pp. 422–429, 1996.
View at: Publisher Site | Google Scholar
N. Smail, A. Messiah, A. Edouard et al., “Role of systemic inflammatory response syndrome and infection in the occurrence of early multiple organ dysfunction syndrome following severe trauma,” Intensive Care Medicine, vol. 21, no. 10, pp. 813–816, 1995.
View at: Publisher Site | Google Scholar
R. M. Durham, J. J. Moran, J. E. Mazuski, M. J. Shapiro, A. E. Baue, and L. M. Flint, “Multiple organ failure in trauma patients,” Journal of Trauma, vol. 55, no. 4, pp. 608–616, 2003.
View at: Publisher Site | Google Scholar
F. Hildebrand, P. Giannoudis, M. Van Griensven et al., “Secondary effects of femoral instrumentation on pulmonary physiology in a standardised sheep model: what is the effect of lung contusion and reaming?” Injury, vol. 36, no. 4, pp. 544–555, 2005.
View at: Publisher Site | Google Scholar
H. C. Pape, “Effects of changing strategies of fracture fixation on immunologic changes and systemic complications after multiple trauma: damage control orthopedic surgery,” Journal of Orthopaedic Research, vol. 26, no. 11, pp. 1478–1484, 2008.
View at: Publisher Site | Google Scholar
P. V. Giannoudis, V. T. Veysi, H. C. Pape, C. Krettek, and M. R. Smith, “When should we operate on major fractures in patients with severe head injuries?” American Journal of Surgery, vol. 183, no. 3, pp. 261–267, 2002.
View at: Publisher Site | Google Scholar
T. Tsukamoto and H. C. Pape, “Animal models for trauma research: what are the options?” Shock, vol. 31, no. 1, pp. 3–10, 2009.
View at: Publisher Site | Google Scholar
N. Marklund and L. Hillered, “Animal modelling of traumatic brain injury in preclinical drug development: where do we go from here?” British Journal of Pharmacology, vol. 164, no. 4, pp. 1207–1229, 2011.
View at: Publisher Site | Google Scholar
M. Frink, H. Andruszkow, C. Zeckey, C. Krettek, and F. Hildebrand, “Experimental trauma models: an update,” Journal of Biomedicine and Biotechnology, vol. 2011, Article ID 797383, 15 pages, 2011.
View at: Publisher Site | Google Scholar
B. D. Semple, N. Bye, M. Rancan, J. M. Ziebell, and M. C. Morganti-Kossmann, “Role of CCL2 (MCP-1) in traumatic brain injury (TBI): evidence from severe TBI patients and CCL2-/- mice,” Journal of Cerebral Blood Flow and Metabolism, vol. 30, no. 4, pp. 769–782, 2010.
View at: Publisher Site | Google Scholar
E. Lloyd, K. Somera-Molina, L. J. Van Eldik, D. M. Watterson, and M. S. Wainwright, “Suppression of acute proinflammatory cytokine and chemokine upregulation by post-injury administration of a novel small molecule improves long-term neurologic outcome in a mouse model of traumatic brain injury,” Journal of Neuroinflammation, vol. 5, article no. 28, 2008.
View at: Publisher Site | Google Scholar
Y. Shapira, E. Shohami, A. Sidi, D. Soffer, S. Freeman, and S. Cotev, “Experimental closed head injury in rats: mechanical, pathophysiologic, and neurologic properties,” Critical Care Medicine, vol. 16, no. 3, pp. 258–265, 1988.
View at: Google Scholar
Y. Chen, S. Constantini, V. Trembovler, M. Weinstock, and E. Shohami, “An experimental model of closed head injury in mice: pathophysiology, histopathology, and cognitive deficits,” Journal of Neurotrauma, vol. 13, no. 10, pp. 557–568, 1996.
View at: Google Scholar
M. Van Griensven, M. Kuzu, M. Breddin et al., “Polymicrobial sepsis induces organ changes due to granulocyte adhesion in a murine two hit model of trauma,” Experimental and Toxicologic Pathology, vol. 54, no. 3, pp. 203–209, 2002.
View at: Google Scholar
J. Meixensberger and K. Roosen, “Clinical and pathophysiological significance of severe neurotrauma in polytraumatized patients,” Langenbeck's Archives of Surgery, vol. 383, no. 3-4, pp. 214–219, 1998.
View at: Publisher Site | Google Scholar
T. A. Gennarelli, H. R. Champion, W. S. Copes, and W. J. Sacco, “Comparison of mortality, morbidity, and severity of 59,713 head injured patients with 114,447 patients with extracranial injuries,” Journal of Trauma, vol. 37, no. 6, pp. 962–968, 1994.
View at: Google Scholar
M. Maegele, D. Engel, B. Bouillon et al., “Incidence and outcome of traumatic brain injury in an urban area in western Europe over 10 years,” European Surgical Research, vol. 39, no. 6, pp. 372–379, 2007.
View at: Publisher Site | Google Scholar
A. Ayala, M. M. Perrin, D. R. Meldrum, W. Ertel, and I. H. Chaudry, “Hemorrhage induces an increase in serum TNF which is not associated with elevated levels of endotoxin,” Cytokine, vol. 2, no. 3, pp. 170–174, 1990.
View at: Google Scholar
J. Jiang, K. Tian, and H. Chen, “Changes of plasma cytokines in patients with severe trauma and their relationship with organ damage,” Zhonghua wai ke za zhi [Chinese journal of surgery], vol. 35, no. 7, pp. 406–407, 1997.
View at: Google Scholar
S. A. Ross, M. I. Halliday, G. C. Campbell, D. P. Byrnes, and B. J. Rowlands, “The presence of tumour necrosis factor in CSF and plasma after severe head injury,” British Journal of Neurosurgery, vol. 8, no. 4, pp. 419–425, 1994.
View at: Google Scholar
J. C. Goodman, C. S. Robertson, R. G. Grossman, and R. K. Narayan, “Elevation of tumor necrosis factor in head injury,” Journal of Neuroimmunology, vol. 30, no. 2-3, pp. 213–217, 1990.
View at: Google Scholar
E. Shohami, R. Bass, D. Wallach, A. Yamin, and R. Gallily, “Inhibition of tumor necrosis factor alpha (TNFα) activity in rat brain is associated with cerebroprotection after closed head injury,” Journal of Cerebral Blood Flow and Metabolism, vol. 16, no. 3, pp. 378–384, 1996.
View at: Google Scholar
S. M. Knoblach, L. Fan, and A. I. Faden, “Early neuronal expression of tumor necrosis factor-α after experimental brain injury contributes to neurological impairment,” Journal of Neuroimmunology, vol. 95, no. 1-2, pp. 115–125, 1999.
View at: Publisher Site | Google Scholar
M. Maegele, P. Riess, S. Sauerland et al., “Characterization of a new rat model of experimental combined neurotrauma,” Shock, vol. 23, no. 5, pp. 476–481, 2005.
View at: Publisher Site | Google Scholar
M. Van Griensven, C. Krettek, and H. C. Pape, “Immune reactions after trauma,” European Journal of Trauma, vol. 29, no. 4, pp. 181–192, 2003.
View at: Publisher Site | Google Scholar
J. W. Berman, M. P. Guida, J. Warren, J. Amat, and C. F. Brosnan, “Localization of monocyte chemoattractant peptide-1 expression in the central nervous system in experimental autoimmune encephalomyelitis and trauma in the rat,” Journal of Immunology, vol. 156, no. 8, pp. 3017–3023, 1996.
View at: Google Scholar
K. A. Harkness, J. D. Sussman, G. A. B. Davies-Jones, J. Greenwood, and M. N. Woodroofe, “Cytokine regulation of MCP-1 expression in brain and retinal microvascular endothelial cells,” Journal of Neuroimmunology, vol. 142, no. 1-2, pp. 1–9, 2003.
View at: Publisher Site | Google Scholar
I. Thibeault, N. Laflamme, and S. Rivest, “Regulation of the gene encoding the monocyte chemoattractant protein 1 (MCP-1) in the mouse and rat brain in response to circulating lps and proinflammatory cytokines,” Journal of Comparative Neurology, vol. 434, no. 4, pp. 461–477, 2001.
View at: Publisher Site | Google Scholar
M. M. Aguilar, F. D. Battistella, J. T. Owings, S. A. Olson, and K. MacColl, “Posttraumatic lymphocyte response: a comparison between peripheral blood T cells and tissue T cells,” Journal of Trauma, vol. 45, no. 1, pp. 14–18, 1998.
View at: Publisher Site | Google Scholar
R. Lundblad, P. Ekstrøm, and K. E. Giercksky, “Pentoxifylline improves survival and reduces tumor necrosis factor, interleukin-6, and endothelin-1 in fulminant intra-abdominal sepsis in rats,” Shock, vol. 3, no. 3, pp. 210–215, 1995.
View at: Google Scholar
M. T. Coccia, K. Waxman, M. H. Soliman, G. Tominaga, and L. Pinderski, “Pentoxifylline improves survival following hemorrhagic shock,” Critical Care Medicine, vol. 17, no. 1, pp. 36–38, 1989.
View at: Google Scholar
M. Maegele, S. Sauerland, B. Bouillon et al., “Differential immunoresponses following experimental traumatic brain injury, bone fracture and “two-hit”-combined neurotrauma,” Inflammation Research, vol. 56, no. 8, pp. 318–323, 2007.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2012 C. Probst 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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