Akademik Veri Yönetim Sistemi
BRATISLAVA MEDICAL JOURNAL, 2026 (SCI-Expanded, Scopus)
Maternal nutrition influences offspring brain development, and omega-3 fatty acids have been linked to neuroprotection. However, their effects on acute responses to traumatic brain injury (TBI) in adult offspring have not been examined. Wistar rat dams (n = 21) received fish oil (0.5 g/kg/day), flaxseed oil (0.5 g/kg/day), or water by gavage during lactation (postnatal days (PND): 1-21). Adult male offspring (n = 32; 8 per group) underwent diffuse TBI using the modified Marmarou weight-drop model. Electrocorticography (ECoG) was recorded at baseline, 24 h, and 72 h post-injury. Somatosensory evoked potentials (SSEPs) were measured on day 3, and thalamic tissue was analyzed by immunohistochemistry for NeuN, S100, and GFAP. TBI induced significant prolongation of N2 (p < 0.05) and P3 (p < 0.01) SSEP latencies versus controls, along with significantly reduced thalamic NeuN expression (p < 0.001) and increased S100 (p < 0.01) and GFAP (p < 0.01) immunoreactivity. In the fish oil group, P3 latency was significantly shorter than in TBI (p < 0.05), and NeuN expression was significantly higher (p < 0.05), indicating preserved neuronal integrity. In the flaxseed oil group, GFAP immunoreactivity was significantly lower than in TBI (p < 0.01); however, NeuN did not differ from TBI and was significantly lower than Control (p < 0.05), and S100 was significantly higher than Control (p < 0.05), indicating incomplete normalization. N2 latency did not differ significantly between supplementation groups and TBI. ECoG spectral power analysis revealed no significant intergroup differences across any frequency band (all p > 0.05). These exploratory findings suggest that the two omega-3 sources exerted marker-specific differential effects rather than uniform neuroprotection: maternal fish oil supplementation was associated with preserved thalamic neuronal integrity and shorter late-latency cortical processing time, whereas flaxseed oil was associated with reduced astrocytic GFAP activation. Given the modest sample, and the acute 72-hour observation window, all findings should be regarded as preliminary and hypothesis-generating. Larger, adequately powered, sex-stratified studies with biochemical validation and longer follow-up are needed to confirm these results.