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A Preclinical Controlled Cortical Impact Model for Traumatic Hemorrhage Contusion and Neuroinflammation
Published on: June 10, 2020
Anti-Inflammatory Therapies for Treatment of Inflammation-Related Preterm Brain Injury
Jaya D Prasad1, Katherine C Gunn1, Joanne O Davidson1
1Department of Physiology, Faculty of Medical and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland 1010, New Zealand.
Insights
Preventing preterm brain injury may be possible by inhibiting peripheral immune responses. This review explores anti-inflammatory agents as a potential neuroprotective strategy for inflammation-related brain injury in preterm infants.
Area of Science:
- Neonatal immunology
- Neuroscience
- Developmental neuroscience
Background:
- Preterm brain injury is common, with no current neuroprotective treatments for inflammation-related damage.
- Perinatal infection and inflammation cause neuroinflammation, cytokine release, and gliosis, impacting brain development and cell survival.
- This neuroinflammation is linked to both immediate and long-term neurological deficits.
Purpose of the Study:
- To review neonatal immunity, neuroinflammation, and mechanisms of brain injury in preterm infants.
- To explore the potential of anti-inflammatory agents as neurotherapeutics for preterm brain injury.
Main Methods:
- Literature review of neonatal immunity and neuroinflammation.
- Analysis of mechanisms linking inflammation to preterm brain injury.
- Evaluation of anti-inflammatory therapies for neuroprotection.
Main Results:
- Infection and inflammation trigger significant neuroinflammatory responses in neonates.
- These inflammatory pathways are critical in the development of preterm brain injury.
- Inhibiting peripheral immune responses is a plausible therapeutic hypothesis.
Conclusions:
- Targeting peripheral inflammation offers a potential strategy to reduce preterm brain injury.
- Anti-inflammatory agents warrant further investigation for neuroprotective efficacy in preterm infants.
- Understanding neonatal immune responses is key to developing effective treatments.
Abstract:
Despite the prevalence of preterm brain injury, there are no established neuroprotective strategies to prevent or alleviate mild-to-moderate inflammation-related brain injury. Perinatal infection and inflammation have been shown to trigger acute neuroinflammation, including proinflammatory cytokine release and gliosis, which are associated with acute and chronic disturbances in brain cell survival and maturation. These findings suggest the hypothesis that the inhibition of peripheral immune responses following infection or nonspecific inflammation may be a therapeutic strategy to reduce the associated brain injury and neurobehavioral deficits. This review provides an overview of the neonatal immunity, neuroinflammation, and mechanisms of inflammation-related brain injury in preterm infants and explores the safety and efficacy of anti-inflammatory agents as potentially neurotherapeutics.
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