- Research article
- Open Access
Intracerebroventricular administration of chondroitinase ABC reduces acute edema after traumatic brain injury in mice
© Finan et al. 2016
- Received: 16 December 2015
- Accepted: 29 February 2016
- Published: 12 March 2016
Brain edema is a significant challenge facing clinicians managing severe traumatic brain injury (TBI) in the acute period. If edema reaches a critical point, it leads to runaway intracranial hypertension that, in turn, leads to severe morbidity or death if left untreated. Clinical data on the efficacy of standard interventions is mixed. The goal of this study was to validate a novel therapeutic strategy for reducing post-traumatic brain edema in a mouse model. Prior in vitro work reported that the brain swells due to coupled electrostatic and osmotic forces generated by large, negatively charged, immobile molecules in the matrix that comprises brain tissue. Chondroitinase ABC (ChABC) digests chondroitin sulfate proteoglycan, a molecule that contributes to this negative charge. Therefore, we administered ChABC by intracerebroventricular (ICV) injection after controlled cortical impact TBI in the mouse and measured associated changes in edema.
Almost half of the edema induced by injury was eliminated by ChABC treatment.
ICV administration of ChABC may be a novel and effective method of treating post-traumatic brain edema in the acute period.
- Traumatic brain injury
- Chondroitinase ABC
Traumatic brain injury (TBI) is responsible for 36 % of deaths among children 1–14 years old and is a leading cause of death among those in the 15–45 year age-bracket . It is also responsible for 40 % of combat deaths among US military personnel . Brain edema within the rigid confines of the skull elevates intracranial pressure (ICP)  and, in severe cases, leads to herniation of the brain tissue which is frequently fatal . Elevated ICP occludes blood vessels causing cerebral hypoperfusion, and elevated ICP correlates with poor outcome . Unfortunately, currently available tools for managing post-traumatic edema suffer from serious limitations. Draining cerebrospinal fluid (CSF) compensates for the increased volume of the brain to a point, but the volume of CSF available to drain is often less than that needed to accommodate severe edema. Hyper-osmotic solutions of saline or mannitol can be administered systemically to draw water out of the brain. However, the subsequent reduction of ICP is sometimes short-lived and may be followed by rebound of ICP to or above the pre-treatment level . Some surgeons perform decompressive craniectomies to relieve ICP in refractory cases. Clinical trial data on the effectiveness of this intervention is currently lacking , and the risk of infection and injury to the brain at the edge of the craniectomy are important drawbacks . In summary, there is an urgent clinical need for new therapeutic strategies to address post-traumatic brain edema.
Coupled electrostatic and osmotic forces cause edema in injured brain tissue [9, 10]. In brain, as in many biological tissues, an ionic solution permeates a porous, solid matrix containing large, immobile, negatively charged molecules. The negatively charged molecules that are bound to the solid phase of the tissue electrostatically attract ions from the intracellular and extracellular fluid, thereby increasing the ion-concentration within the tissue as compared to the fluid surrounding the tissue and creating an osmotic gradient that draws in water. A field of biomechanics known as triphasic theory quantitatively describes these coupled electrostatic and osmotic forces . Previously we have shown that biologically inert (i.e. dead) brain tissue swells in a manner that conforms to the highly non-linear predictions of triphasic theory, validating this model . The healthy brain is highly metabolic, and much of the energy generated by metabolism is used to regulate ion concentrations in the tissue . Therefore, healthy brain tissue is normally far from thermodynamic equilibrium, and its volume is less than that predicted by the physical laws of triphasic theory. However, when the brain is injured and ion flux out of cells is compromised, either because of reduced metabolism or damaged cell membranes, the damaged tissue moves toward thermodynamic equilibrium, i.e. it swells.
This physical model of post-traumatic brain edema motivated our therapeutic strategy. One of the most abundant of the large, immobile, negatively charged molecules in the tissue that drive edema is chondroitin sulfate proteoglycan (CSPG) . CSPG also has a very low pKa (between 3 and 4 depending on the ionic strength of the solution ), meaning that it is very negatively charged at physiological pH. Chondroitinase ABC (ChABC) is an enzyme that degrades CSPG, thereby mobilizing its negative charge. This allows it to diffuse out of the solid matrix and reduce the osmotic potential to draw in water. ChABC has been studied at length in the central nervous system as a means of breaking down glial scars that inhibit axon regeneration [14–16] and is generally well-tolerated in rodents. For example, there was no change in visual field or acuity after ChABC was injected into the visual cortex in mice . In addition to being generated in response to injury during scar formation, CSPGs exist throughout the brain in the absence of injury. They are abundant in perineuronal nets, extracellular structures that surround neurons and inhibit synaptic plasticity . Previous in vitro work by our group showed that ChABC reduced edema in dead and injured brain tissue . Therefore, we hypothesized that administration of ChABC would reduce post-traumatic brain edema in the mouse model of controlled cortical impact (CCI) TBI.
All animal procedures were conducted according to the guidelines set forth in the Guide for the Care and Use of Laboratory Animals  and were approved by the Institutional Animal Care and Use Committee at Columbia University. A total of 40 mice were used in this study. Ten week old male C57/BL6 mice were anesthetized with isoflurane and placed in a stereotactic frame. The skull was exposed, and a 5 mm diameter craniotomy was drilled to the left of the sagittal suture between lambda and bregma. An Impact One device (Leica Biosystems, Buffalo Grove, IL) was used to propel a 3 mm diameter, flat-ended, cylindrical indenter into the brain to a depth of 1.3 mm at a speed of 5 ms−1 with a dwell time of 300 ms at a 10° angle to the vertical. In uninjured controls, the skull was exposed but not opened to eliminate the risk of damage during the craniotomy. The treatment consisted of 10 μl of a filter-sterilized 50 U/ml solution of ChABC (Sigma Aldrich, St. Louis, MO) dissolved in PBS. Within 5 min after injury, ChABC or vehicle was administered to the right lateral ventricle using a Hamilton syringe with a 26G needle inserted to a depth of 3 mm at a location 1 mm to the right and 0.3 mm anterior to bregma . In preliminary experiments, a green tracer dye was injected to verify that agents injected at this point permeated the ventricular network. A group of uninjured animals was also injected to measure the effect of ChABC on water content in healthy brain tissue. To evaluate the effect of treatment 5 min after injury on edema 24 h after injury, animals were euthanized by cervical dislocation under deep anesthesia at the 24 h time point and the brains were immediately removed. A 4 mm thick coronal slice of brain tissue encompassing the lesion site was cut from the mid-brain and split into two hemispheres (ipsilateral and contralateral to the injury). Each hemisphere was weighed, dried at 95° C for 72 h, and then weighed again to determine the water fraction.
There are several clinically established treatments for brain edema, and others have been proposed. However, none of the established or proposed treatments employs the same mechanism of action as ChABC treatment, suggesting that ChABC treatment would offer additional benefits when applied in combination with other established or proposed treatments for brain edema. Established treatments such as elevation of the head, CSF drainage, hyperosmotic therapy and decompressive craniectomy do not alter the fixed charge density, which is the target of ChABC treatment. Inhibition of aquaporin 4 (AQP4) has been proposed as a treatment for brain edema . Aquaporin 4 is a water channel in the blood brain barrier (BBB). Genetic deletion of AQP4 reduced brain swelling after stroke by about a third , prompting an ongoing search for a small molecule that inhibits AQP4. Such a treatment would complement rather than replace ChABC treatment because AQP4 inhibition increases the resistance to water flow across the BBB while ChABC treatment reduces the osmotic pressure driving that flow. Another recently proposed treatment for brain edema employs an osmotic transport device that is placed on the exposed cortex to draw water out of the tissue . Chondroitinase ABC treatment would again complement this therapy because it would reduce the competing osmotic pressure that tends to hold water in the tissue.
The ICV route of administration was selected because it offered a combination of efficacy and clinical convenience. Intraparenchymal injection of ChABC in mice affects only a small region of the brain around the injection site and therefore may be inappropriate for treating more widespread edema . Intravenous delivery is impractical because ChABC is too large to cross an intact BBB. A ventricular shunt is typically placed in patients with severe TBI to drain CSF as a first-line therapy to combat edema and control ICP . This shunt can be used to administer therapeutic agents. Idursulfase, an enzyme with a similar substrate, successfully permeates brain tissue when administered to primates via ICV injection , suggesting that ICV delivery of ChABC would be similarly successful. In our study, an efficacious dose of ChABC was delivered via the ventricular space remote from the site of injury, suggesting that this strategy can be used to address global edema using ventricular shunts that are routinely placed as part of first-line therapy. However, the murine brain is much smaller than the human brain and the lissencephalic anatomy may allow easier access to the swollen cortex than the gyrencephalic anatomy of the human brain. Therefore, ICV delivery may be less effective in the human. Another important limitation of the current study is that treatment was administered within 5 min post-injury. The time to reach, stabilize and transport a severely brain injured patient creates an unavoidable delay of several hours between injury and treatment. Further investigation is necessary to fully understand how the timing of the therapeutic dose influences the time course of post-injury edema. Unfortunately, a thorough investigation of time course may require a different animal model. In humans, the brain is massive and is confined within the rigid cranial vault. This confinement creates positive feedback between edema, intracranial pressure and ischemia. This phenomenon is known as runaway intracranial hypertension and it strongly influences the course of post-traumatic edema in the days following a severe TBI. In mice, the brain is smaller and the skull is more flexible so this feedback effect is weaker. Therefore, the model presented here is appropriate to the study of post-traumatic edema but not for the study of subsequent runaway intracranial hypertension. Nevertheless, these preliminary results show that chondroitinase ABC can mitigate post-traumatic edema in vivo and this indicates that it may mitigate runaway intracranial hypertension in humans.
This study demonstrated that ICV administration of ChABC eliminated almost half of the edema induced by CCI TBI in mice. Chondroitinase ABC has been tested extensively in the mouse brain for other purposes (i.e. not for treating edema) without evidence of toxicity [14–17]. Therefore, we believe that ChABC may be a promising new therapy for addressing post-traumatic brain edema.
JDF designed and executed the experiments, analyzed the data and drafted the manuscript. FSC assisted with experimental design and execution. SGK and BMIII supervised the study, assisted with experimental design and interpretation of the results and reviewed the manuscript. All authors read and approved the final manuscript.
The authors would like to acknowledge excellent technical assistance from Autumn Kim and Tony Yu. John D. Finan received a Charles H. Revson Senior Biomedical Fellowship from the Charles H. Revson Foundation. This research was made possible in part by a grant from the Research Initiatives in Science & Engineering competition, sponsored by Columbia University’s Office of the Executive Vice President for Research.
Barclay Morrison III and John D. Finan are named inventors on U.S. Patent US9040040 B2 ‘Enzyme Combinations to Reduce Brain Tissue Swelling’.
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- Hoyert DL, Heron MP, Murphy SL, Kung HC. Deaths: final data for 2003. Natl Vital Stat Rep. 2006;54(13):1–120.PubMedGoogle Scholar
- Eastridge BJ, Hardin M, Cantrell J, Oetjen-Gerdes L, Zubko T, Mallak C, Wade CE, Simmons J, Mace J, Mabry R, et al. Died of wounds on the battlefield: causation and implications for improving combat casualty care. J Trauma. 2011;71(1 Suppl):S4–8.View ArticlePubMedGoogle Scholar
- Unterberg AW, Stover J, Kress B, Kiening KL. Edema and brain trauma. Neuroscience. 2004;129(4):1021–9.View ArticlePubMedGoogle Scholar
- Brain Trauma Foundation, American Association of Neurological Surgeons, Congress of Neurological Surgeons, Joint Section on Neurotrauma and Critical Care, AANS/CNS, Bratton SL, Chestnut RM, Ghajar J, McConnell Hammond FF, Harris OA et al. Guidelines for the management of severe traumatic brain injury. VIII. Intracranial pressure thresholds. J Neurotrauma 2007; 24 (Suppl 1):S55–58.Google Scholar
- Marmarou A, Anderson RL, Ward JD, Choi SC, Young HF, Eisenberg HM, Foulkes MA, Marshall LF, Jane JA. Impact of ICP instability and hypotension on outcome in patients with severe head trauma. J Neurosurg. 1991;75:S59–66.Google Scholar
- Node Y, Nakazawa S. Clinical study of mannitol and glycerol on raised intracranial pressure and on their rebound phenomenon. Adv Neurol. 1990;52:359–63.PubMedGoogle Scholar
- Cooper DJ, Rosenfeld JV, Murray L, Arabi YM, Davies AR, D’Urso P, Kossmann T, Ponsford J, Seppelt I, Reilly P, et al. Decompressive craniectomy in diffuse traumatic brain injury. N Engl J Med. 2011;364(16):1493–502.View ArticlePubMedGoogle Scholar
- Honeybul S, Ho KM. Long-term complications of decompressive craniectomy for head injury. J Neurotrauma. 2011;28(6):929–35.View ArticlePubMedGoogle Scholar
- Elkin BS, Shaik MA, Morrison B 3rd. Fixed negative charge and the Donnan effect: a description of the driving forces associated with brain tissue swelling and oedema. Philos Trans A Math Phys Eng Sci. 1912;2010(368):585–603.Google Scholar
- Elkin BS, Shaik MA, Morrison B 3rd. Chondroitinase ABC reduces brain tissue swelling in vitro. J Neurotrauma. 2011;28(11):2277–85.View ArticlePubMedGoogle Scholar
- Lai WM, Hou JS, Mow VC. A triphasic theory for the swelling and deformation behaviors of articular cartilage. J Biomech Eng. 1991;113(3):245–58.View ArticlePubMedGoogle Scholar
- Raichle ME, Gusnard DA. Appraising the brain’s energy budget. Proc Natl Acad Sci USA. 2002;99(16):10237–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Rueda C, Arias C, Galera P, Lopez-Cabarcos E, Yague A. Mucopolysaccharides in aqueous solutions: effect of ionic strength on titration curves. Farmaco. 2001;56(5–7):527–32.View ArticlePubMedGoogle Scholar
- Bradbury EJ, Moon LD, Popat RJ, King VR, Bennett GS, Patel PN, Fawcett JW, McMahon SB. Chondroitinase ABC promotes functional recovery after spinal cord injury. Nature. 2002;416(6881):636–40.View ArticlePubMedGoogle Scholar
- Houle JD, Tom VJ, Mayes D, Wagoner G, Phillips N, Silver J. Combining an autologous peripheral nervous system “bridge” and matrix modification by chondroitinase allows robust, functional regeneration beyond a hemisection lesion of the adult rat spinal cord. J Neurosci. 2006;26(28):7405–15.View ArticlePubMedGoogle Scholar
- Harris NG, Nogueira MS, Verley DR, Sutton RL. Chondroitinase enhances cortical map plasticity and increases functionally active sprouting axons after brain injury. J Neurotrauma. 2013;30(14):1257–69.View ArticlePubMedPubMed CentralGoogle Scholar
- Pizzorusso T, Medini P, Berardi N, Chierzi S, Fawcett JW, Maffei L. Reactivation of ocular dominance plasticity in the adult visual cortex. Science. 2002;298(5596):1248–51.View ArticlePubMedGoogle Scholar
- Miyata S, Kitagawa H. Mechanisms for modulation of neural plasticity and axon regeneration by chondroitin sulphate. J Biochem. 2015;157(1):13–22.View ArticlePubMedGoogle Scholar
- Institute for Laboratory Animal Research. Guide for the care and use of laboratory animals. Washington, D. C: National Academy Press; 2011.Google Scholar
- DeVos SL, Miller TM. Direct intraventricular delivery of drugs to the rodent central nervous system. J Vis Exp. 2013;75:e50326.PubMedGoogle Scholar
- McBride DW, Szu JI, Hale C, Hsu MS, Rodgers VG, Binder DK. Reduction of cerebral edema after traumatic brain injury using an osmotic transport device. J Neurotrauma. 2014;31(23):1948–54.View ArticlePubMedPubMed CentralGoogle Scholar
- Cheng T, Wang W, Li Q, Han X, Xing J, Qi C, Lan X, Wan J, Potts A, Guan F, et al. Cerebroprotection of flavanol (−)-epicatechin after traumatic brain injury via Nrf2-dependent and -independent pathways. Free Radic Biol Med. 2015;92:15–28.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhao M, Liang F, Xu H, Yan W, Zhang J. Methylene blue exerts a neuroprotective effect against traumatic brain injury by promoting autophagy and inhibiting microglial activation. Mol Med Rep. 2016;13(1):13–20.PubMedPubMed CentralGoogle Scholar
- Krieg SM, Sonanini S, Plesnila N, Trabold R. Effect of small molecule vasopressin V1a and V2 receptor antagonists on brain edema formation and secondary brain damage following traumatic brain injury in mice. J Neurotrauma. 2015;32(4):221–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Yao X, Uchida K, Papadopoulos MC, Zador Z, Manley GT, Verkman AS. Mildly reduced brain swelling and improved neurological outcome in aquaporin-4 knockout mice following controlled cortical impact brain injury. J Neurotrauma. 2015;32(19):1458–64.View ArticlePubMedGoogle Scholar
- Manley GT, Fujimura M, Ma T, Noshita N, Filiz F, Bollen AW, Chan P, Verkman AS. Aquaporin-4 deletion in mice reduces brain edema after acute water intoxication and ischemic stroke. Nat Med. 2000;6(2):159–63.View ArticlePubMedGoogle Scholar
- Brain Trauma Foundation and American Association of Neurological Surgeons. Guidelines for the management of severe traumatic brain injury. J Neurotrauma. 2007;24(Suppl 1):S1–106.Google Scholar
- Calias P, Papisov M, Pan J, Savioli N, Belov V, Huang Y, Lotterhand J, Alessandrini M, Liu N, Fischman AJ, et al. CNS penetration of intrathecal-lumbar idursulfase in the monkey, dog and mouse: implications for neurological outcomes of lysosomal storage disorder. PLoS One. 2012;7(1):e30341.View ArticlePubMedPubMed CentralGoogle Scholar