Abstract

BackgroundConcussions account for the majority of traumatic brain injuries (TBI) and can result in cumulative damage, neurodegeneration, and chronic neurological abnormalities. The underlying mechanisms of these detrimental effects remain poorly understood and there are presently no specific treatments for concussions. Neuroinflammation is a major contributor to secondary damage following more severe TBI, and recent findings from our laboratory suggest it may be involved in the cumulative properties of repeated concussion. We previously found that an anti-CD11d monoclonal antibody that blocks the CD11d/CD18 integrin and adhesion molecule interaction following severe experimental TBI reduces neuroinflammation, oxidative activity, and tissue damage, and improves functional recovery. As similar processes may be involved in repeated concussion, here we studied the effects of the anti-CD11d treatment in a rat model of repeated concussion.MethodsRats were treated 2 h and 24 h after each of three repeated mild lateral fluid percussion injuries with either the CD11d antibody or an isotype-matched control antibody, 1B7. Injuries were separated by a five-day inter-injury interval. After the final treatment and either an acute (24 to 72 h post-injury) or chronic (8 weeks post-injury) recovery period had elapsed, behavioral and pathological outcomes were examined.ResultsThe anti-CD11d treatment reduced neutrophil and macrophage levels in the injured brain with concomitant reductions in lipid peroxidation, astrocyte activation, amyloid precursor protein accumulation, and neuronal loss. The anti-CD11d treatment also improved outcome on tasks of cognition, sensorimotor ability, and anxiety.ConclusionsThese findings demonstrate that reducing inflammation after repeated mild brain injury in rats leads to improved behavioral outcomes and that the anti-CD11d treatment may be a viable therapy to improve post-concussion outcomes.

Highlights

  • Concussions account for the majority of all traumatic brain injuries (TBI) and are recognized as a serious global health concern, in individuals at an increased risk of suffering concussion, such as athletes and military personnel [1,2,3]

  • Since neuroinflammation may be implicated in concussion [24], and occurs following mild lateral fluid percussion injuries (mLFP) [5,24,25,26], here we evaluated the effects of the CD11d monoclonal antibody (mAb) treatment in the repeated mLFP rat model of repeated concussion

  • We report that treatment with the CD11d mAb after each of three repeated mLFP reduced neutrophil and macrophage numbers, astrocyte activation, and lipid peroxidation

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Summary

Introduction

Concussions account for the majority of all traumatic brain injuries (TBI) and are recognized as a serious global health concern, in individuals at an increased risk of suffering concussion, such as athletes and military personnel [1,2,3]. The anti-CD11d treatment reduced leukocyte levels in the injured brain with concomitant reductions in astrocyte activation, lipid peroxidation, axonal injury, and neuronal loss [18]. We report that treatment with the CD11d mAb after each of three repeated mLFP reduced neutrophil and macrophage numbers, astrocyte activation, and lipid peroxidation. These reductions in mediators of secondary injury were accompanied by reductions in neuronal loss, axonal injury, and behavioral deficits. We previously found that an anti-CD11d monoclonal antibody that blocks the CD11d/CD18 integrin and adhesion molecule interaction following severe experimental TBI reduces neuroinflammation, oxidative activity, and tissue damage, and improves functional recovery. As similar processes may be involved in repeated concussion, here we studied the effects of the anti-CD11d treatment in a rat model of repeated concussion

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