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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Pediatric concussions can result in long-term sequelae with physiological and psychological perturbations. This pediatric concussion mouse model results in long-term neuroinflammation, white matter alterations, and neuronal modifications with behavioral dysfunction. The model can be adapted to differential impact locations or repeated concussions to assess lifetime changes.

Abstract

Concussions and mild traumatic brain injuries (mTBI) during childhood represent a significant health endangerment, with many patients later in life exhibiting debilitating physiological, neurological, and psychosocial outcomes. The cellular and molecular pathophysiological mechanisms are relatively unknown, and this significant gap effectively precludes investigations into specific therapeutic strategies to mitigate chronic sequelae. No single animal concussion model recapitulates all the features reported in human subjects, and current models are designed to answer specific research questions. We set out to develop a juvenile concussion that recapitulates clinical early, and long-term symptomology encountered, termed Closed Head Injury with Long-term Disorder (CHILD). In this model, a concussive force via an electromagnetic impactor is delivered to the head of a lightly anesthetized unrestrained post-natal day 17 (P17) mouse, allowing free rotation of the head. Mice are placed on a tightly stretched tin foil across a stereotactic device, and the impactor is carefully aligned with the targeted cortical region. The electromagnetic impactor facilitates the selection of impact depth, dwell, and duration to determine injury severity. A strength of this model is that it allows head rotation, an important clinical feature. After impact, mice are immediately monitored for righting time and time to explore their environment, followed by their return to their dam. Increasing the severity of concussion results in intracranial bleeds in a subset of mice. Mice can be routinely monitored for behavior and neuroimaging over their lifespan, as desired. Various injury severities mimic the heterogeneous nature of juvenile concussions. The current standard CHILD model exhibits no skull fracture, no observable conventional neuroimaging change (similar to clinical), but leads to progressive and persistent neuronal death, altered diffusion MRI, modified neuronal activity and plasticity, increased gliosis, and progressive behavioral perturbations with age. In summary, this CHILD model mimics the early and long-term features observed in many clinical concussion patients.

Introduction

Pediatric Traumatic Brain Injury (TBI) is a major health concern as it represents the leading cause of pediatric emergency medical care visits and is associated with debilitating health outcomes later in life. Even mild TBI (mTBI), which makes up 75% of all TBI cases1, leads to long-term abnormalities, including physiological, psychological, neurological, and cognitive dysfunctions2. Despite the high occurrence of pediatric mTBI and its significant associated health risks, the pathological, cellular, and molecular mechanisms that precede the chronic deficits are still underexplored. This gap in knowledge impedes the deve....

Protocol

Experiments were reproduced on 2 sites, the University of Bordeaux (France) and the University of California Riverside (CA, USA).

In Bordeaux, all experiments were performed on male and female P17 C57Bl6J mice bred in the University animal facility. Initial breeders were obtained from a commercial source and raised under standard conditions with a 12/12-h dark/light cycle, a temperature of 21 °C ± 1 °C, and a humidity of 55% ± 10%, and food and water provided ad libitum. Experimental procedures are in accordance with the University of Bordeaux Animal Care Committee regulations, French laws governing laboratory a....

Representative Results

The CHILD model is a relatively rapid and reproducible model of mTBI in pediatric mice, also allowing for variations in severity and location. The CHILD mice, as expected, exhibited significantly longer recovery times from closed head injury (Figure 3). When cohorts (n = 36 female sham, n = 140 male sham, n = 30 female G1, n = 55 male G1, n = 32 female G2, n = 141 male G2) were aggregated, a delay in righting time was observed (Figure 3A, 3-way ANOVA p .......

Discussion

Critical steps in the protocol
The CHILD protocol described here requires the use of an electromagnetic impactor (Figure 2A) that (1) standardizes the impact parameters (speed, depth, duration), (2) ensures reproducibility within and across laboratories, and (3) is readily available commercially. Another critical component is the impactor tip that strikes the rodent's head. A variety of possibilities can be used, ranging from silicone to metal tips, but this protoc.......

Disclosures

The authors have nothing to disclose.

Acknowledgements

This method paper was funded by Eranet Neuron Neuvasc (Badaut), Agence Nationale de la Recherche Nanospace (Badaut), CNRS IRP IINOVAtion (Badaut) and NIH NINDS Grant No. 1R01NS119605 (Obenaus, Badaut) and 1RF1NS138032 (Obenaus, Territo). Figure 1 is created with BioRender.com.

....

Materials

NameCompanyCatalog NumberComments
BSASigma Aldrich Chimie S.a.r.l
80 Rue de Luzais
L'lsle-d'Abeau Chesnes - BP701
38297 Saint-Quentin-Fallavier Cedex
France
A7030
C57Bl6J mice Charles River Laboratory France CRLF 9 All. Moulin Berger, 69130 Écully, FranceBordeaux
Electromagnetic impactorLeica Biosystems, Richmond, IL USAImpact One stereotaxic impactor
Epifluorescence microscopeOlympus, BX41, Center Valley, PA
Ethylen glycolSigma Aldrich Chimie S.a.r.l
80 Rue de Luzais
L'lsle-d'Abeau Chesnes - BP701
38297 Saint-Quentin-Fallavier Cedex
France
102466
GFAP primary antibodyMillipore, Billerica, MAAB5541chicken anti-GFAP
GFAP secondary antibodyMolecular Probes, InvitrogenA11034goat anti-rabbit AlexaFluor  488
GlycerolSigma Aldrich Chimie S.a.r.l
80 Rue de Luzais
L'lsle-d'Abeau Chesnes - BP701
38297 Saint-Quentin-Fallavier Cedex
France
G5516
Heavy duty aluminium foilKirklandRK611obtained at Cosco
Micromanager software (NIH, USA
NeuN primary antibodyAbCam, Discovery Drive, Cambridge
Biomedical Campus,
Cambridge, CB2 0AX, UK
AB128886rabbit anti-NeuN
NeuN secondary antibodyMolecular Probes, InvitrogenA11041goat anti-chicken AlexaFluor 568
PBSSigma Aldrich Chimie S.a.r.l
80 Rue de Luzais
L'lsle-d'Abeau Chesnes - BP701
38297 Saint-Quentin-Fallavier Cedex
France
P5493
PFASigma Aldrich Chimie S.a.r.l
80 Rue de Luzais
L'lsle-d'Abeau Chesnes - BP701
38297 Saint-Quentin-Fallavier Cedex
France
1.04003
Sodium azideSigma Aldrich Chimie S.a.r.l
80 Rue de Luzais
L'lsle-d'Abeau Chesnes - BP701
38297 Saint-Quentin-Fallavier Cedex
France
26628-22-8
Stereotaxic frame - baseKOPF instruments 7324 Elmo St, Tujunga, CA 91042, États-Unis900-C
Stereotaxic frame - electrode manipulatorKOPF instruments 7324 Elmo St, Tujunga, CA 91042, États-Unis960
Stereotaxic frame - u-frameKOPF instruments 7324 Elmo St, Tujunga, CA 91042, États-Unis900-U
Triton x-100Sigma Aldrich Chimie S.a.r.l
80 Rue de Luzais
L'lsle-d'Abeau Chesnes - BP701
38297 Saint-Quentin-Fallavier Cedex
France
X100
VectashieldVector laboratoriesH-1000-10Mounting medium
VibratomeLeica Biosystems, Richmond, IL USAVTS1000
Jackson laboratory The Jackson Laboratory 600 Main Street Bar Harbor, ME USA 04609UCR

References

  1. Dewan, M. C., et al. Estimating the global incidence of traumatic brain injury. J Neurosurg. 130 (4), 1080-1097 (2018).
  2. Rivara, F. P., et al. Persistence of disability 24 to 36 months after pediatri....

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