The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Adaptation of the Fluid Percussion Injury Model to the Mouse
Abstract
Fluid percussion injury (FPI) is a well-characterized experimental model of traumatic brain injury (TBI) in the rat. Many pathophysiologic consequences and mechanisms of recovery after TBI rely on neurochemical pathways that can be examined in genetically altered mice. Therefore, FPI applied to mice may be a useful experimental tool to investigate TBI at the molecular level. In the present study, we establish FPI as a viable model of TBI in the mouse by characterizing acute neurological, histopathological, and behavioral changes. Right-sided parasagittal FPI or sham treatment was administered in male C57BL/6 mice. Acute neurological evaluation revealed righting reflexes in the injured animals (p < 0.001). Deficits in spatial learning and memory were observed in the Morris water maze (MWM) 5 and 6 days after injury. A novel MWM data analysis protocol is described. The injured group (n = 18) demonstrated impaired performance in the MWM during acquisition (p < 0.05) and probe trials (p < 0.025) compared to sham animals (n = 16). At 7 days postinjury, glial fibrillary acidic protein immunohistochemistry revealed intense cortical, callosal, and hippocampal gliosis. The modified Gallyas silver degeneration stain consistently labeled cell bodies and terminals throughout the ipsilateral cortex, axons in the gray matter-white matter interface above the corpus callosum and within the corpus callosum bilaterally, and terminals and fibers in the thalamus bilaterally. Additionally, the mo…
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“Many biological pathways are disrupted by experimental TBI resulting in progressive neurodegeneration including atrophy, neuronal loss, and axonal degeneration which are often associated with neuroinflammation including macrophage reactivity (82–85).”
From The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease (2018) · cites this paper as [82]
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Items 101–145 of 145
Vishwanath, M., Jafarlou, S., Shin, I., Dutt, N. D., Rahmani, A. M., Lim, M. M., & Cao, H. (2020) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc44109.2020.9175915 · Cited by 12
“Once the hub was FPI-induced and monitored till the stage of toe pinch withdrawal reflex, a 20-ms pulse of saline was delivered onto the dura with the pressure level in between 1.4 and 2.1 atm [18, 19].”
MethodInfluentialCerebral Concussion Primes the Lungs for Subsequent Neutrophil-Mediated Injury
Humphries, D. C., O’Neill, S., Scholefield, E., Dorward, D. A., MacKinnon, A. C., Rossi, A. G., Haslett, C., Andrews, P., Rhodes, J. K. J., & Dhaliwal, K. (2018) · Critical Care Medicine · doi:10.1097/ccm.0000000000003270 · Cited by 12
“5 ATM FPI in Mice Induces a Unilateral Cortical Insult With Cerebral Inflammatory Cell Influx and No Measureable Clinical Sequelae Mice received a lateral FPI using an established methodology (14).”
MethodEpileptogenesis following experimentally induced traumatic brain injury – a systematic review
Chandel, S., Gupta, S., & Medhi, B. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2015-0050 · Cited by 14
“The midline FPI model was initially developed for use in cats, rabbits, and rats; it was later modified to produce the lateral FPI (LFPI) model in rodents (Dixon et al., 1987; Hayes et al., 1987; McIntosh et al., 1987; McIntosh et al., 1989; Härtl et al., 1997; Carbonell et al., 1998).”
MethodMuthuraju, S., Pati, S., Rafiqul, M., Abdullah, J., & Jaafar, H. (2012) · Basal Ganglia · doi:10.1016/j.baga.2012.06.004 · Cited by 13
“1 atm [4] was rapidly injected into the cranial cavity.”
BackgroundLateral (Parasagittal) Fluid Percussion Model of Traumatic Brain Injury.
Van, K. C., & Lyeth, B. G. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3816-2_14 · Cited by 13
Suppressive silver methods--a tool for identifying axotomy-induced neuron degeneration.
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“Argyrophilic nerve cell bodies have been described following penetrating trauma [87], blunt trauma [12,13,17,64,87], ischemia”
BackgroundModified device for fluid percussion injury in rodents
Ouyang, W., Wu, W.-H., Fan, Z., Wang, J.-H., Pan, H.-J., & Yang, W.-B. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24261 · Cited by 11
“In the study of Carbonell et al. (1998), a 2.0-mm diameter circular site over the parietal cortex, at 0.5 mm lateral to the sagittal suture, and 0.5 mm caudal to bregma, was used LFP; while in the study of Shultz et al. (2014) and M. R. Johnstone et al. (2018), a 3.0 mm craniotomy window more…”
BackgroundMethodResultInfluentialMuthuraju, S., Pati, S., Rafiqul, M., Abdullah, J., & Jaafar, H. (2013) · Journal of Biosciences · doi:10.1007/s12038-012-9290-7 · Cited by 11
“A pulse of 21–23 ms at 3.6±0.1 atm (Carbonell et al. 1998) was rapidly injected into the cranial cavity.”
BackgroundMethodInfluentialThe subventricular zone responds dynamically to mechanical brain injuries
Dizon, M. L. V., & Szele, F. G. (2006) · doi:10.1007/0-387-31389-3_7 · Cited by 11
“The majority of fluid percussion injury studies have been performed in rat, but this model can also be used in mouse (Carbonell et al., 1998), and we have found that numbers of BrdU labelled cells increase in mouse after a percussion injury of the cerebral cortex (Ramaswamy et al.”
BackgroundBeitchman, J. A., Lifshitz, J., Harris, N., Thomas, T. C., Lafrenaye, A. D., Hånell, A., Dixon, C. E., Povlishock, J., & Rowe, R. K. (2020) · bioRxiv · doi:10.1089/neur.2020.0046 · Cited by 10
“clinical relevance of these injuries includes a transient suppression of neurological reflexes and acute motor deficits [5, 6, 10, 12-28].”
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Kaniuk, J. K., Kumar, D., Mazurek, C. Y., Khavari, S., Sollenberger, C. H., Ahuja, A., Mossner, J. M., & Ahuja, C. S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157191 · Cited by 11
“The FPI model was originally established in rabbits, but has since been adopted to murine models in the 1980s [129,130].”
VanderGiessen, M., de Jager, C., Leighton, J., Xie, H., Theus, M. H., Johnson, E. A., & Kehn‐Hall, K. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1514940 · Cited by 9
Epilepsy After Traumatic Brain Injury
Pitkänen, A., Kyyriäinen, J., Andrade, P., Pasanen, L., & Ndode‐Ekane, X. E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804066-9.00046-8 · Cited by 42
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“Single TBI of moderate severity was induced using the lateral fluid percussion injury (LFPI) apparatus, adjusted to the mouse [78,79].”
MethodDella-Pace, I. D., de Souza, T. L., Grauncke, A. C. B., Rambo, L., Ribeiro, L., Cipolatto, R. P., Severo, L., Papalia, W. L., Santos, A., Facundo, V., et al. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.02.040 · Cited by 8
Neuroprotective effect of triptolide on neuronal inflammation in rats with mild brain injury
Fang, Z., Shen, G., Lou, C., Botchway, B. O. A., Lu, Q., Yang, Q.-N., & Amin, N. (2024) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2024.05.007 · Cited by 6
“…TNF-α ) was much higher in studies on neuronal injury, cerebral ischemia, and inflammation, which intensified the inflammatory response (Lisman et al., 2017; Wang et al., 2021a; Carbonell et al., 1998) and promoted the transcription of IL-1 β and NF-κ B in brain tissue (Carbonell and Grady, 1999).”
BackgroundAnimal models for the study of military-related, blast-induced traumatic brain injury
McCabe, J., Moratz, C., Liu, Y.-B., Egan, R., Chen, H., Liu, J., Budinich, C. S., Burton, E. E., Danquah, J. K., & Myers, M. (2010) · 2010 Biomedical Sciences and Engineering Conference · doi:10.1109/bsec.2010.5510803 · Cited by 6
Deficits in ERK and CREB activation in the hippocampus after traumatic brain injury
Atkins, C. M., Falo, M. C., Alonso, O. F., Bramlett, H. M., & Dietrich, W. D. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.04.064 · Cited by 77
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Models of Rodent Cortical Traumatic Brain Injury
Corrigan, F., Ziebell, J. M., & Vink, R. (2011) · Neuromethods · doi:10.1007/978-1-61779-301-1_11 · Cited by 5
A Mouse Model of Temporal Lobe Contusion
Simard, J. M., Tosun, Ç., Tsymbalyuk, O., Moyer, M. B., Keledjian, K., Tsymbalyuk, N., Olaniran, A., Evans, M., Langbein, J., Khan, Z., et al. (2024) · Journal of Neurotrauma · doi:10.1089/neu.2024.0242 · Cited by 3
Traumatic Brain Injury Models in Zebrafish (Danio rerio)
Babchenko, V. Y., Belova, A. S., Bashirzade, A. A., Tikhonova, M. A., Demin, K. A., Zabegalov, K. N., Petersen, E. V., Kalueff, A. V., & Amstislavskaya, T. G. (2022) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-022-01254-y · Cited by 4
Correction to: A new multiple trauma model of the mouse
Fitschen-Oestern, S., Lippross, S., Klueter, T., Weuster, M., Varoga, D., Tohidnezhad, M., Pufe, T., Rose-John, S., Andruszkow, H., Hildebrand, F., et al. (2019) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-018-2330-1 · Cited by 3
Dvilevicius, A. E., Prandini, M. N., Dobrowolski, S., & Barbosa, A. C. D. C. (2008) · Brazilian Neurosurgery · doi:10.1055/s-0038-1625529 · Cited by 3
Research and Publishing in Neurosurgery
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“Also of practical importance is that recent investigations show that gliomas having loss of Ip and 19q are more sensitive for alkylating cytostatic drugs such as the combination therapy Procarbazine, CCNU, Vincristine (PCV) or Temozolomide [9].”
BackgroundMethodInfluentialUbri, C., Farrugia, A. M., & Cohen, A. S. (2025) · Journal of Neurotrauma · doi:10.1089/neu.2025.0046 · Cited by 2
“…our laboratory has demonstrated that experimentally inducing mild TBI using the well-established lateral fl uid percussion injury (LFPI) model 109 – 111 decreases mPFC network excitation that is essential to ef fi cacious neurotransmission, 112 highlighting the mPFC ’ s vulnerability to mild TBI.”
Janković, T., Bumber, J. R., Gržeta, N., Dolenec, P., Jaeger, M., Križ, J., Župan, G., & Pilipović, K. (2025) · Biomedicines · doi:10.3390/biomedicines13010218 · Cited by 1
Experimental study of a novel mouse model of tibial shaft fracture combined with blunt chest trauma
Zhang, B., Fu, T., Han, Y., Li, G., Wan, X.-Y., & Li, Y. (2024) · Animal Models and Experimental Medicine · doi:10.1002/ame2.12379 · Cited by 1
“20,21 This model can be considered for patients with multiple injuries, including TBI, but its limitation is that it cannot accurately reflect the clinical environment and intensive monitoring after trauma.”
Vishwanath, M., Cao, S., Dutt, N., Rahmani, A. M., Lim, M. M., & Cao, H. (2023) · arXiv.org · doi:10.48550/arxiv.2310.02398 · Cited by 1
“1 atm Carbonell et al. (1998); McIntosh et al. (1989). The procedure was identical for sham mice, except for the introduction of the fluid pulse.”
MethodKomoltsev, I., Salyp, O., Volkova, A., Bashkatova, D., Shirobokova, N., Frankevich, S., Shalneva, D., Kostyunina, O., Chizhova, O., Kostrukov, P., et al. (2023) · Neurology International · doi:10.3390/neurolint15020038 · Cited by 1
“LFPI in both rats [20] and mice [21] causes focal damage in the neocortex of the ipsilateral hemisphere (in the visual, sensorimotor, auditory, and parietal regions) [22].”
BackgroundHarleen, S., Kimberly, J. N., & Ann, M. (2013) · InTech eBooks · doi:10.5772/53268 · Cited by 1
“A traumatic lesion to the brain cortex results in an increase in proliferation of NSCs in the SVZ, although varied locations and degrees of injury have resulted in an incongruity of re‐ sults across the literature [93-98].”
BackgroundThe Fluid Percussion Injury Rodent Model in Preclinical Research on Traumatic Brain Injury
Clausen, F., Hillered, L., & Marklund, N. (2019) · Neuromethods · doi:10.1007/978-1-4939-9711-4_1 · Cited by 1
Animal Models of Traumatic Brain Injury
Kochanek, P. M., & Dixon, C. E. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00330-0 · Cited by 3
Iannucci, J., Sentmanat, A., Dickerson, K., Obaid, M., Bandopadhyay, S., Houghton, A., Arisi, G. M., & Shapiro, L. A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27209127
“Studies in rats [30,31] and mice [34] show that the extent of neuropathology and neurobehavioral impairment depends largely on injury location and severity.”
Yu, Y., Wang, C., Zhu, J., Du, J.-H., Li, H., Ning, S., Yang, R., Ma, Y., Yuan, M.-Y., Shen, W., et al. (2026) · Neuroprotection · doi:10.1002/nep3.70044
“Several experimental rodent models are utilized to simulate human TBI, with controlled cortical impact (CCI), fl uid percussion injury (FPI), 16 and weight ‐ drop injury (WDI) 17,18 are the most commonly used.”
Surles-Zeigler, M. C., Sincomb, T., Dixon, C. E., Imam, F. T., Gillespie, T., Grethe, J. S., Ferguson, A. R., & Martone, M. E. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.29.564650
Tauopathies in Traumatic Brain Injury
Pace, J., Shammassian, B. H., & Hoffer, S. A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812344-7.00009-1
Schurman, L. D. (2018) · doi:10.25772/8t1v-rt57
“MWM Fixed Platform acquisition deficits (Carbonell et al, 1998; Spain et al, 2010) have been shown in right hemisphere injury, though contrary to the present findings, others have noted acquisition deficits also from left lateral injuries (Tchantchou and Zhang, 2013; Fox et al, 1999).”
BackgroundResultFluid percussion model of traumatic brain injury
Rowe, R. K., Griffiths, D. R., & Lifshitz, J. (2018) · doi:10.1007/978-1-4939-8564-7_6
Powell, M. A. (2016) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/s1cq-ce32
“(1987), FPI has been successfully modified for mice (Carbonell et al., 1998) and”
Memory Disruption Following Traumatic Brain Injury
Berman, R. F., Lyeth, B. G., Shahlaie, K., & Gurkoff, G. G. (2015) · Springer eBooks · doi:10.1007/978-3-319-15759-7_13
Neuroprotective strategies for traumatic brain injury
Yin, T. C. (2015) · doi:10.17077/etd.c8l4gi2h
A Cellular Mechanism for Dendritic Spine Loss Following Traumautic Brain Injury in Rat
Low, B. (2009) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/y1xg-db87
“Amongst the 44 injured animals, the average pressure pulse was 2.226 ± 0.013 atm and the average righting time was 384 ± 12 seconds, which correspond to a moderate injury (Morehead et al., 1994; Schmidt and Grady, 1995; Carbonell et al., 1998; Hallam et al., 2004).”
BackgroundInfluential
Metadata
- Authors
- CARBONELL, W. S., MARIS, D. O., McCALL, T., & GRADY, M. S.
- Affiliations
- University of Washington (US)
- ORCID
- CARBONELL, W. SHAWN
- Venue
- Journal of Neurotrauma
- Publisher
- SAGE Publications
- Published
- 1998-03
- Volume
- 15
- Issue
- 3
- Pages
- 217-229
- ISSN
- 0897-7151 (ISSN-L)
- 1557-9042
- OpenAlex
- W1978835755
- Cited by
- 157
- References
- 0
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 6 · 2023: 4 · 2022: 2 · 2021: 6 · 2020: 7 · 2019: 10 · 2018: 10 · 2017: 10 · 2016: 13 · 2015: 5 · 2014: 9 · 2013: 11 · 2012: 4
- FWCI
- 1.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurotrauma (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Washington
- National Institutes of Health (5p50ns030305-05, 5r01ns033107-03)
- National Institute of Neurological Disorders and Stroke (NS-30305, NS33107)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury and Neurovascular Disturbances
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury Research
- Physical Sciences › Engineering › Biomedical Engineering › Automotive and Human Injury Biomechanics
- Keywords
- fluid percussion injury, traumatic brain injury, mouse model, spatial learning and memory, Morris water maze, gliosis, glial fibrillary acidic protein, corpus callosum, thalamus, righting reflex, behavioral deficits
- MeSH terms
- Animals, Brain Injuries, Postural Balance, Glial Fibrillary Acidic Protein, Gliosis, Male, Mice, Inbred C57BL, Neuroglia, Neurons, Silver Staining, Maze Learning, Mice, Rats
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