Journal
MOLECULAR NEUROBIOLOGY
Volume 59, Issue 2, Pages 1018-1040Publisher
SPRINGER
DOI: 10.1007/s12035-021-02654-w
Keywords
Astrocytes; Microglia; Foetal growth retardation; Immune cells; Blood-brain barrier; Neonatal brain injury
Categories
Funding
- National Health and Medical Research Council (Australia) [APP1147545]
- Royal Brisbane and Women's Hospital Foundation
- Children's Hospital Foundation [50217]
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Inflammation plays a key role in the progression of brain impairment in FGR newborns, and ibuprofen may reduce NVU disruption and brain impairment in FGR piglets. Ibuprofen treatment decreases pro-inflammatory response, enhances astrocyte interaction with blood vessels, and restores NVU integrity, improving the FGR brain microenvironment.
The developing brain is particularly vulnerable to foetal growth restriction (FGR) and abnormal neurodevelopment is common in the FGR infant ranging from behavioural and learning disorders to cerebral palsy. No treatment exists to protect the FGR newborn brain. Recent evidence suggests inflammation may play a key role in the mechanism responsible for the progression of brain impairment in the FGR newborn, including disruption to the neurovascular unit (NVU). We explored whether ibuprofen, an anti-inflammatory drug, could reduce NVU disruption and brain impairment in the FGR newborn. Using a preclinical FGR piglet model, ibuprofen was orally administered for 3 days from birth. FGR brains demonstrated a proinflammatory state, with changes to glial morphology (astrocytes and microglia), and blood-brain barrier disruption, assessed by IgG and albumin leakage into the brain parenchyma and a decrease in blood vessel density. Loss of interaction between astrocytic end-feet and blood vessels was evident where plasma protein leakage was present, suggestive of structural deficits to the NVU. T-cell infiltration was also evident in the parenchyma of FGR piglet brains. Ibuprofen treatment reduced the pro-inflammatory response in FGR piglets, reducing the number of activated microglia and enhancing astrocyte interaction with blood vessels. Ibuprofen also attenuated plasma protein leakage, regained astrocytic end-feet interaction around vessels, and decreased T-cell infiltration into the FGR brain. These findings suggest postnatal administration of ibuprofen modulates the inflammatory state, allowing for stronger interaction between vasculature and astrocytic end-feet to restore NVU integrity. Modulation of the NVU improves the FGR brain microenvironment and may be key to neuroprotection.
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