Communication publiée dans un ouvrage (Colloques et congrès scientifiques)
Hypoxic-Ischemic Encephalopathy and Premature Babies Brain Damage: Impact of Estetrol
Tskitishvili, Ekaterine; Nisolle, Michelle; Noël, Agnès et al.
2015In The 11th Congress of the European Society of Gynecology, Prague 21-24 October, 2015
Peer reviewed
 

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Mots-clés :
Hypoxic-Ischemic Encephalopathy; Estetrol; Premature Babies Brain Damage
Résumé :
[en] Neonatal hypoxic-ischemic brain injury remains a main problem of perinatal medicine. About 20% of affected newborns die in the postnatal period, and an additional 25% will sustain childhood disabilities mostly in the form of motor and cognitive delays. The nature of the deficits is dependent on the gestational age and severity of the insult, though it is s seldom reported in preterm infants. No medical treatment provides important neuroprotection against HIE. Studies in animal models of HIE may provide important information for the development of treatment for this pathological condition. Estetrol (E4) is a recently described estrogen with four hydroxyl-groups that is synthesized exclusively during pregnancy by the human fetal liver. In this study, we defined the antioxidative effect of E4 in primary hippocampal cell cultures taken from newborn rat pups (in vitro) and evaluated its neuroprotective and therapeutic potency in neonatal HIE model of the immature newborn rat (in vivo). Lactate Dehydrogenase (LDH) and cell survival (MTS) assays were performed on primary neuronal cell cultures. Rat pups body temperatures were examined along with their body and brain weights. Brains were studied at the level of the hippocampus and cortex. Intact cell counting and expressions of markers for neuronal cell viability (microtubule-associated protein-2 (MAP-2)), neurogenesis (doublecortin (DCX)) and angiogenesis (vascular-endothelial growth factor (VEGF)) were evaluated by histo- and immunohistochemistry. The serum levels of two markers of brain damage (S100B and glial fibrillary acidic protein (GFAP)) were measured by ELISA. Our results demonstrate that E4 has a significant neuroprotective and therapeutic dose-dependent effects. Estetrol has powerful antioxidative and cell survival effects in vitro. It decreases the early gray matter loss and promotes neuro- and angiogenesis in vivo. Estetrol treatment has no effects on body weight, brain weight or body temperature. Taken together, Estetrol might become an important safe and physiological substance to treat neonatal HIE.
Disciplines :
Médecine de la reproduction (Gynécologie, andrologie, obstétrique)
Auteur, co-auteur :
Tskitishvili, Ekaterine  ;  Université de Liège > GIGA-Research
Nisolle, Michelle ;  Université de Liège > Département des sciences cliniques > Gynécologie - Obstétrique
Noël, Agnès  ;  Université de Liège > Département des sciences cliniques > Labo de biologie des tumeurs et du développement
Foidart, Jean-Michel ;  Université de Liège > Département des sciences cliniques > Département des sciences cliniques
Langue du document :
Anglais
Titre :
Hypoxic-Ischemic Encephalopathy and Premature Babies Brain Damage: Impact of Estetrol
Date de publication/diffusion :
2015
Nom de la manifestation :
The 11th Congress of the European Society of Gynecology
Lieu de la manifestation :
Prague, République Tchèque
Date de la manifestation :
From 21-10-2015 to 24-10-2015
Manifestation à portée :
International
Titre de l'ouvrage principal :
The 11th Congress of the European Society of Gynecology, Prague 21-24 October, 2015
Peer review/Comité de sélection :
Peer reviewed
Disponible sur ORBi :
depuis le 09 novembre 2015

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