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Overexpression of Mfsd2a attenuates blood brain barrier dysfunction via Cav-1/Keap-1/Nrf-2/HO-1 pathway in a rat model of surgical brain injury.
- Source :
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Experimental neurology [Exp Neurol] 2020 Apr; Vol. 326, pp. 113203. Date of Electronic Publication: 2020 Jan 16. - Publication Year :
- 2020
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Abstract
- Introduction: Disruption of the blood brain barrier (BBB) and subsequent cerebral edema formation is one of the major adverse effects of brain surgery, leading to postoperative neurological dysfunction. Recently, Mfsd2a has been shown to have a crucial role for the maintenance of BBB functions. In this study, we aimed to evaluate the role of Mfsd2a on BBB disruption following surgical brain injury (SBI) in rats.<br />Materials and Methods: Rats were subjected to SBI by partial resection of the right frontal lobe. To evaluate the effect of Mfsd2a on BBB permeability and neurobehavior outcome following SBI, Mfsd2a was either overexpressed or downregulated in the brain by administering Mfsd2a CRISPR activation or knockout plasmids, respectively. The potential mechanism of Mfsd2a-mediated BBB protection through the cav-1/Nrf-2/HO-1 signaling pathway was evaluated.<br />Results: Mfsd2a levels were significantly decreased while cav-1, Nrf-2 and HO-1 levels were increased in the right frontal perisurgical area following SBI. When overexpressed, Mfsd2a attenuated brain edema and abolished neurologic impairment caused by SBI while downregulation of Mfsd2a expression further deteriorated BBB functions and worsened neurologic performance following SBI. The beneficial effect of Mfsd2a overexpression on BBB functions was associated with diminished expression of cav-1, increased Keap-1/Nrf-2 dissociation and further augmented levels of Nrf-2 and HO-1 in the right frontal perisurgical area, leading to enhanced levels of tight junction proteins following SBI. The BBB protective effect of Mfsd2a was blocked by selective inhibitors of Nrf-2 and HO-1.<br />Conclusions: Mfsd2a attenuates BBB disruption through cav-1/Nrf-2/HO-1 signaling pathway in rats subjected to experimental SBI.<br />Competing Interests: Declaration of Competing Interest The authors have disclosed that they do not have any conflicts of interest.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Behavior, Animal
Body Water metabolism
Brain Injuries genetics
Brain Injuries therapy
Caveolin 1 genetics
Frontal Lobe injuries
Genetic Therapy
Heme Oxygenase (Decyclizing) genetics
Kelch-Like ECH-Associated Protein 1 genetics
Male
NF-E2-Related Factor 2 genetics
Rats
Rats, Sprague-Dawley
Treatment Outcome
Blood-Brain Barrier physiopathology
Brain Injuries physiopathology
Signal Transduction genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2430
- Volume :
- 326
- Database :
- MEDLINE
- Journal :
- Experimental neurology
- Publication Type :
- Academic Journal
- Accession number :
- 31954682
- Full Text :
- https://doi.org/10.1016/j.expneurol.2020.113203