Dawood, A. (2019). Vulnerability of adult hippocampus to toxicity after postnatal exposure of nursing male albino rats to iron overload : Histomorphometric and ultrastructural study. Journal of Medical Histology, 3(1), 77-101. doi: 10.21608/jmh.2019.13247.1057
Asmaa Dawood. "Vulnerability of adult hippocampus to toxicity after postnatal exposure of nursing male albino rats to iron overload : Histomorphometric and ultrastructural study". Journal of Medical Histology, 3, 1, 2019, 77-101. doi: 10.21608/jmh.2019.13247.1057
Dawood, A. (2019). 'Vulnerability of adult hippocampus to toxicity after postnatal exposure of nursing male albino rats to iron overload : Histomorphometric and ultrastructural study', Journal of Medical Histology, 3(1), pp. 77-101. doi: 10.21608/jmh.2019.13247.1057
Dawood, A. Vulnerability of adult hippocampus to toxicity after postnatal exposure of nursing male albino rats to iron overload : Histomorphometric and ultrastructural study. Journal of Medical Histology, 2019; 3(1): 77-101. doi: 10.21608/jmh.2019.13247.1057
Vulnerability of adult hippocampus to toxicity after postnatal exposure of nursing male albino rats to iron overload : Histomorphometric and ultrastructural study
Department of Histology, Faculty of Medicine, Assiut University, Assiut, Egypt, Department of Biomedical Science, Faculty of Medicine, King Faisal University, Alhasa, Saudi Arabia
Abstract
Background: The association of iron overload with neurodegenerative diseases and cognitive deficits in aging were previous reported. Developing hippocampus is highly sensitive to changes in iron homeostasis that might lead to long term irreversible impact on its functions. Objective: To examine the possible histopathological changes in adult hippocampal subregions CA1, CA3 and DG subjected to excess iron administration at critical early postnatal life. Materials and Methods: 20 male rat pups weighing 50-55gm were selected and randomly divided into 2 groups (10 per each). The control received 0.5 ml normal saline intraperitoneally once daily for 21 consecutive days. Iron treated group received intraperitoneal injection of ferrous sulfate dissolved in 0.5 ml normal saline at a dose of 3 mg/kg/day for 21 days. After sacrifice, brain specimens were processed for histomorphometric and ultrastructural study. Results: Iron deposits were reported only in treated group using Prussian blue. Obvious degeneration of principal neurons with significant decrease in their number and increased immunoreactivity to caspase 3 and glial fibrillary acid protein (GFAP)were observed in all studied subfields of iron treated hippocampus. Astrogliosis, astrocyte damage and disruption of blood brain barrier were also noticed. Conclusion: There was pronounced degenerative changes in all studied subregions of iron treated hippocampus indicating its extreme sensitivity to changes in iron homeostasis, hence iron overload could be considered highly toxic insult on growing hippocampal tissue.
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