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Efficacy of Nitric Oxide-Releasing Nanofibers in Reducing Renal Ischemia-Reperfusion Injury in a Rat Model

Authors
Ko, HyunminKim, Jin SugShin, Jae HoJeong, Kyung HwanAhn, Hyung Joon
Issue Date
Jan-2022
Publisher
INT SCIENTIFIC INFORMATION, INC
Keywords
Kidney Transplantation; Nanofibers; Nitric Oxide
Citation
ANNALS OF TRANSPLANTATION, v.27
Journal Title
ANNALS OF TRANSPLANTATION
Volume
27
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/74635
DOI
10.12659/AOT.934800
ISSN
1425-9524
Abstract
Background: This study aimed to analyze the preventive effect of nitric oxide (NO)-releasing nanofibers against ischemia-reperfusion injury (IRI) and to determine the mechanism of action as a novel NO delivery system in a rat model. Material/Methods: Eight-week-old male Sprague-Dawley rats, weighing 250 to 280 g, were divided into 3 groups: sham, untreated (n=5); control, renal ischemia injury for 55 min (n=4); and NO24, renal ischemia injury for 55 min with kidney wrapping of NO-releasing nanofiber for 24 h (n=6). mRNA expression was measured by real-time polymerase chain reaction (PCR), whereas protein expression was assessed by immunohistochemistry and western blot analysis. Results: Serum creatinine levels in the sham, control, and NO24 groups were 0.48 +/- 0.08, 4.66 +/- 0.33, and 2.60 +/- 1.00 mg/dL, respectively (P=0.002). Anti-apoptotic Bcl-2 protein expression differed significantly between the control and the NO24 groups (Bcl-2/b-actin; control, 0.50 +/- 0.12; NO24, 1.56 +/- 0.56; P=0.024). mRNA expression level of the inflammatory cytokine tumor necrosis factor-a (TNF-a) was significantly higher in the control group (23.24 +/- 11.32, P=0.016) than in the sham group (1.00 +/- 1.21), and mRNA expression of TNF-a in the NO24 group (1.28 +/- 1.16, P=0.010) was significantly lower than in the control group. Histological analysis revealed decreased atrophy and necrosis in the NO24 group compared to those in the control group. Conclusions: This study demonstrated that kidney wrapping of NO-releasing nanofibers had a protective effect against kidney IRI through anti-apoptotic and anti-inflammatory mechanisms.
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의과대학 (의학부(임상-광명))
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