Abstract

BackgroundPreeclampsia is a systemic, multi‐organ endotheliopathy, associated with oxidative injury to the blood–brain barrier (BBB). Preeclampsia initiates a cascade of events that include neuroinflammation. Recently, it was documented that Wnt/β‐catenin signaling pathway exerts neuroprotective effects and maintain BBB integrity. We investigate the protective effect of omega‐3 against neurovascular complication of preeclampsia and its relation to Wnt/β‐catenin signaling pathway.MethodologyAfter confirmation of day 0 pregnancy (G0), 24 adult pregnant female Wistar rats were divided into four groups control pregnant, pregnant supplemented with omega‐3, preeclampsia (PE); female rats received N (ω)‐nitro‐L‐arginine methyl ester (L‐NAME) (50 mg/kg/day SC from day 7 to day 16 of pregnancy for induction of preeclampsia) and PE rats supplemented with omega‐3. The intake of omega‐3 started on day zero (0) of pregnancy until the end of the study (144 mg/kg\\day orally).ResultsWe found that omega‐3 supplementation significantly improved cognitive functions and EEG amplitude, decreased blood pressure, water contents of brain tissues, sFlt‐1, oxidative stress, proteinuria, and enhanced Wnt\\β‐catenin proteins. Histological examination showed improved cerebral microangiopathy, increased expression of claudin‐1 and ‐3, CD31, and VEGF in the cerebral cortical microvasculature and choroid plexus in PE rats treated with omega‐3. A positive correlation between protein expression level of Wnt \\β‐catenin and cognitive functions, and a negative correlation between claudin‐5 relative expression, claudin‐1 and ‐3 area % from one side and water content of the brain tissues from the other side were observed.ConclusionWnt/β‐catenin signaling pathway suspected to have an important role to improve BBB integrity. Neuroprotective, antioxidant, and anti‐inflammatory effects of omega‐3 were observed and can be suggested as protective supplementation for preeclampsia.

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