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Comparison of the protective effects of selective endothelin-a receptor antagonist, ambrisentan, and dual endothelin-A/B receptor antagonist, Bosentan, in experimental renal ischemia reperfusion injury

dc.contributor.authorKazimoglu H., Uysal E., Dokur M., Gurer A.O., Batcioglu K., Uyumlu B.A., Petekkaya E., Karadag M.
dc.contributor.authorKazimoglu, H, Uysal, E, Dokur, M, Gurer, AO, Batcioglu, K, Uyumlu, BA, Petekkaya, E, Karadag, M
dc.date.accessioned2023-05-09T20:32:56Z
dc.date.available2023-05-09T20:32:56Z
dc.date.issued2020-01-01
dc.date.issued2020.01.01
dc.description.abstractAIM: This study aims to compare the protective effects of ambrisentan, a selective endothelin typeA receptor antagonist, and bosentan, a dual endothelin typeA/B receptor antagonist, on experimental renal ischemia reperfusion injury. METHOD: The study sample consisted of 21 female rats, which were divided into 3 groups: Control, Ambrisentan and Bosentan. For the ischemia-reperfusion injury model, left-kidney nephrectomy was performed after sacrifi cing the animals. In the immunohistochemical examination, caspase-3 was examined, and then the apoptotic index was determined. In the biochemical examination, the activities of malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase, and the levels of nitrite (NOx), TNF-α, and IL-1β were determined. RESULTS: There were statistically signifi cant differences between the groups in terms of total injury score grade in range of 0-3 (p=0.001). The glomerular and tubular apoptotic indices were higher in the control group as compared to those of the ambrisentan and bosentan groups (p=0.001). There were no statistically signifi cant differences in terms of SOD, CAT, GPx, MDA, IL-1β and TNF-α measurements among the groups (p>0.05). CONCLUSIONS: In the experimentally created renal ischemia reperfusion model, both ambrisentan and bosentan increased the NOx level, decreased the apoptosis, and protected the kidney from renal ischemia reperfusion injury. However, no signifi cant superiority was found between ambrisentan and bosentan in terms of their protective effects (Tab. 3, Fig. 2, Ref. 31). Text in PDF www.elis.sk.
dc.identifier.doi10.4149/BLL_2020_091
dc.identifier.eissn1336-0345
dc.identifier.endpage553
dc.identifier.issn0006-9248
dc.identifier.scopus2-s2.0-85088828543
dc.identifier.startpage547
dc.identifier.urihttps://hdl.handle.net/20.500.12597/15178
dc.identifier.volume121
dc.identifier.wosWOS:000571574800005
dc.relation.ispartofBratislava Medical Journal
dc.relation.ispartofBRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY
dc.rightstrue
dc.subjectAmbrisentan | Apoptosis | Bosentan | Ischemia-reperfusion | Kidney | Rat
dc.titleComparison of the protective effects of selective endothelin-a receptor antagonist, ambrisentan, and dual endothelin-A/B receptor antagonist, Bosentan, in experimental renal ischemia reperfusion injury
dc.titleComparison of the protective effects of selective endothelin-a receptor antagonist, ambrisentan, and dual endothelin-A/B receptor antagonist, bosentan, in experimental renal ischemia reperfusion injury
dc.typeArticle
dspace.entity.typePublication
oaire.citation.issue8
oaire.citation.volume121
relation.isScopusOfPublicatione308e8e8-3b63-4072-b1e1-a666614df8da
relation.isScopusOfPublication.latestForDiscoverye308e8e8-3b63-4072-b1e1-a666614df8da
relation.isWosOfPublicationcf9dbe18-0e12-4d01-97ec-4b463faa3a42
relation.isWosOfPublication.latestForDiscoverycf9dbe18-0e12-4d01-97ec-4b463faa3a42

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