Foetal Growth Restriction Effects on Grey and White Matter in the Prefrontal Cortex and Basal Ganglia of Postnatal Day 10 Piglets
View abstract on PubMed
Summary
This summary is machine-generated.Foetal growth restriction (FGR) in piglets leads to brain damage, including reduced neurons and impaired white matter development. This neuroinflammation and cell death may contribute to long-term developmental issues.
Area Of Science
- Neuroscience
- Developmental Biology
- Perinatal Medicine
Background
- Foetal growth restriction (FGR) is linked to placental insufficiency, increasing perinatal risks.
- The developing brain is particularly susceptible to FGR, potentially causing lasting neurodevelopmental deficits.
Purpose Of The Study
- To investigate the neuropathological consequences of FGR in the piglet brain up to postnatal day 10.
- To assess grey and white matter integrity, neuronal survival, and glial activation in FGR piglets.
Main Methods
- Utilized a piglet model of spontaneous FGR and normally grown (NG) littermates.
- Assessed neuropathology in the prefrontal cortex (PFC) and basal ganglia (BG) at postnatal day 10.
- Quantified neuronal markers (NeuN), structural integrity (MAP2), apoptosis (Casp-3, -9), myelination, and glial activation (Iba-1, GFAP).
Main Results
- FGR piglets exhibited decreased neuronal counts and structural integrity in the PFC and BG.
- Increased apoptosis was observed in neuronal and glial cells within the FGR brain.
- Hypomyelination and heightened microglial and astrocyte activation were evident in both grey and white matter of FGR piglets.
Conclusions
- FGR in piglets results in persistent grey and white matter impairments, characterized by increased apoptosis and glial activation in key brain regions.
- These neuropathological changes suggest a potential mechanism for adverse neurodevelopmental outcomes in FGR.
- The findings underscore the need for therapeutic strategies to support brain repair in infants affected by FGR.

