Abstract | BACKGROUND: AIM: The aim of this study was to examine the effect of GSNO on I/R-induced intestine and lung damage and detect the potential mechanisms emphasizing the protective role of GSNO. METHODS: Intestinal I/R was induced by occluding the superior mesenteric artery for 30 min followed by reperfusion for 180 min. GSNO was administered intravenously before reperfusion period (0.25 mg/kg). The levels of lipid peroxidation, reduced glutathione, and myeloperoxidase (MPO), histopathological evaluation and immunohistochemical expressions of both nuclear factor KappaB (NF-κB) and inducible nitric oxide (iNOS) in intestine and lung tissues were assessed. RESULTS: Histolopathologic evaluation demonstrated that intestinal I/R induced severe damages in the intestine and the lung tissues. Histopathological scores decreased with GSNO treatment. GSNO treatment reduced lipid peroxidation and MPO levels and inhibited expression of NF-κB and iNOS in the intestine. CONCLUSION: Our results suggest that GSNO treatment may ameliorate the intestinal and lung injury in rats, at least in part, by inhibiting inflammatory response and oxidative stress.
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Authors | Inci Turan, Hale Sayan Ozacmak, V Haktan Ozacmak, Figen Barut, I Diler Ozacmak |
Journal | Tissue & cell
(Tissue Cell)
Vol. 52
Pg. 35-41
(Jun 2018)
ISSN: 1532-3072 [Electronic] Scotland |
PMID | 29857826
(Publication Type: Journal Article)
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Copyright | Copyright © 2018 Elsevier Ltd. All rights reserved. |
Chemical References |
- NF-kappa B
- Nitric Oxide Donors
- S-Nitrosoglutathione
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Topics |
- Acute Lung Injury
(etiology, metabolism)
- Animals
- Intestines
(drug effects, pathology)
- Male
- NF-kappa B
(metabolism)
- Nitric Oxide Donors
(pharmacology)
- Oxidative Stress
(drug effects)
- Rats
- Rats, Wistar
- Reperfusion Injury
(complications, metabolism)
- S-Nitrosoglutathione
(pharmacology)
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