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Milk Fat Globule-Epidermal Growth Factor VIII Ameliorates Brain Injury in the Subacute Phase of Cerebral Ischemia in an Animal Model

Authors
Choi, Jong-IlKang, Ho-YoungHan, ChoongseongWoo, Dong-HunKim, Jong-HoonPark, Dong-Hyuk
Issue Date
Mar-2020
Publisher
KOREAN NEUROSURGICAL SOC
Keywords
Angiogenesis; Inflammation; MFG-E8; Neurobehavioral outcome; Neuronal proliferation; Subacute cerebral infarction
Citation
JOURNAL OF KOREAN NEUROSURGICAL SOCIETY, v.63, no.2, pp.163 - 170
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF KOREAN NEUROSURGICAL SOCIETY
Volume
63
Number
2
Start Page
163
End Page
170
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/57541
DOI
10.3340/jkns.2019.0188
ISSN
2005-3711
Abstract
Objective : Milk fat globule-epidermal growth factor VIII (MFG-E8) may play a key role in inflammatory responses and has the potential to function as a neuroprotective agent for ameliorating brain injury in cerebral infarction. This study aimed to determine the role of MFG-E8 in brain injury in the subacute phase of cerebral ischemia in a rat model. Methods : Focal cerebral ischemia was induced in rats by occluding the middle cerebral artery with the modified intraluminal filament technique. Twenty-four hours after ischemia induction, rats were randomly assigned to two groups and treated with either recombinant human MFG-E8 or saline. Functional outcomes were assessed using the modified Neurological Severity Score (mNSS), and infarct volumes were evaluated using histology. Anti-inflammation, angiogenesis, and neurogenesis were assessed using immunohistochemistry with antibodies against ionized calcium-binding adapter molecule 1 (Iba-1), rat endothelial cell antigen-1 (RECA-1), and bromodeoxyuridine (BrdU)/doublecortin (DCX), respectively. Results : Our results showed that intravenous MFG-E8 treatment did not reduce the infarct volume; however, the mNSS test revealed that neurobehavioral deficits were significantly improved in the MFG-E8-treated group than in the vehicle group. Immunofluorescence staining revealed a significantly lower number of Iba-1-positive cells and higher number of RECA-1 in the peri-infarcted brain region, and significantly higher numbers of BrdU-and DCX-positive cells in the subventricular zone in the MFG-E8-treated group than in the vehicle group. Conclusion : Our findings suggest that MFG-E8 improves neurological function by suppressing inflammation and enhancing angiogenesis and neuronal proliferation in the subacute phase of cerebral infarction.
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