ePoster

PERINATAL HYPOXIC INJURY MODULATES NEURONAL AND EXTRACELLULAR MATRIX ORGANIZATION IN THE ADULT MIDCINGULATE CORTEX IN RATS

Sara Trnski Levakand 5 co-authors

Croatian Institute for Brain Research, Scientific Centre of Excellence for Basic, Clinical and Translational Neuroscience, School of Medicine, University of Zagreb

FENS Forum 2026 (2026)
Barcelona, Spain
Board PS02-07PM-479

Presentation

Date TBA

Board: PS02-07PM-479

Poster preview

PERINATAL HYPOXIC INJURY MODULATES NEURONAL AND EXTRACELLULAR MATRIX ORGANIZATION IN THE ADULT MIDCINGULATE CORTEX IN RATS poster preview

Event Information

Poster Board

PS02-07PM-479

Abstract

This study examines the effects of short-term perinatal hypoxia in rats on the morphology, distribution, and number of NeuN-positive neurons (NeuN+), parvalbumin-positive neurons (PV+), perineuronal net (PNN) – PV colocalization, and total PNNs in the cortical layers of mature midcingulate cortex (MCC). Forty-eight Wistar Han (RccHan: WIST) rat pups (P1) were randomly assigned to hypoxic or control groups, with sexes equally distributed. Animals were exposed for 2h in a heated chamber to hypoxia (pO 9.73kPa; pATM 46.66kPa) or normoxia (pO 21.20kPa; pATM 101.33kPa). At 3.5 months of age, brain sections were triple-immunofluorescence-stained and analysed for WFA-positive PNNs and colocalization with NeuN+ and PV+ neurons in the MCC (bregma −1.56 to −1.92mm according to the Paxinos and Watson atlas). PNNs displayed a more reticular and condensed morphology in layers II, III, Va, and Vb, and were significantly more numerous following hypoxia. PV+ neurons were also significantly increased in the hypoxic group, especially in layer I. PNNs surrounded PV+ neurons throughout the MCC. However, following hypoxia, more numerous PNNs were observed that did not associate with PV+, but instead surrounded NeuN+ neurons in layers II, III, Va, and Vb. These findings indicate that perinatal hypoxia induces permanent, structural, cortical-layer-specific neuronal and ECM reorganization in MCC as a plasticity response to a moderate lesion.
(Acknowledgements: Croatian Science Foundation: HRZZ-IP-2024-05-4135 and DOK-NPOO-2023-10-7312; PK.1.1.10.0009.)

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