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Dr. Nessrine Ebrahim Ahmed Salem :: Publications:

Title:
Attenuation of brain injury by transplantation of bone marrow-derived mesenchymal stem cells in an experimental model of neonatal hypoxic-ischemic encephalopathy
Authors: Nesrine EBRAHIM1, Eman EHSAN2, Eman Abd EL GHANY2, Dina SABRY3, Ashraf SHAMAA4
Year: 2019
Keywords: cerebral cortex, neonatal hypoxic ischemia, stem cells.
Journal: Not Available
Volume: Not Available
Issue: Not Available
Pages: Not Available
Publisher: Not Available
Local/International: International
Paper Link: Not Available
Full paper Nessrine Ebrahim Ahmed Salem_BIOCELL MS 6111 Ebrahim E1 R1 E2 R2 Ef.docx
Supplementary materials Not Available
Abstract:

Abstract: The neonatal hypoxic-ischemic encephalopathy (HIE) is an important cause of neurological morbidity and mortality in neonates. Cell therapy is considered a promising method for treating severe neurological disorders such as this one. Stem cells have the capacity for self-renewal and differentiation into certain cell lineages. The present study was aimed to find out the most beneficial route of bone marrow derived mesenchymal stem cells (BMSCs) administration for the attenuation of experimentally induced HIE in neonatal rats. Sixty neonatal rats were divided randomly into four groups. Group I: control group. Group II: rats were exposed to bilateral ligation of cephalic arteries. Group ΙIΙ: rats were exposed to bilateral ligation of cephalic arteries and then underwent intravenous (i.v.) BMSCs injection. Group ΙV: rats were exposed to bilateral ligation of cephalic arteries and then underwent intracerebroventricular (I.C.V) BMSCs injection. The animals were evaluated by (a) neurobehavioral tests; (b) histopathology, i.e. histological and immuno-histochemical studies; and (3) gene expression studies. The BMSCs treated groups (III and IV) showed improvement in neurobehavioral tests, histopathological studies, and gene expression, as compared to non-injected lesioned rats (group II) with better improvement in group IV (I.C.V. injections) than in group III (i.v. injections).

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