ACLS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Altunoluk, B.
Right arrow Articles by Fadillioglu, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Altunoluk, B.
Right arrow Articles by Fadillioglu, E.
Annals of Clinical & Laboratory Science 36:326-332 (2006)
© 2006 Association of Clinical Scientists

An Angiotensin-Converting Enzyme Inhibitor, Zofenopril, Prevents Renal Ischemia/Reperfusion Injury in Rats

Bulent Altunoluk1, Haluk Soylemez2, Fatih Oguz2, Emine Turkmen3 and Ersin Fadillioglu4
1 Division of Urology, State Hospital of Kahramanmaras, Kaharamanmaras; 2 Departments of Urology and 3 Pathology, Faculty of Medicine, Inonu University, Malatya; and 4 Department of Physiology, Faculty of Medicine, Hacettepe University, Ankara; Turkey

Address correspondence to Ersin Fadillioglu, M.D., Department of Physiology, Faculty of Medicine, Hacettepe University, Ankara 06100, Turkey; tel 90 312 305 1567; fax 90 312 310 0580; e-mail efadillioglu{at}yahoo.com.

Zofenopril ameliorates experimental cardiac ischemia/reperfusion (IR) injury in animal models and exhibits beneficial cardiovascular effects in patients with myocardial infarction. The objective of the present research was to investigate whether zofenopril can protect against renal IR injury. Rats were divided into 4 experimental groups: (a) control, (b) IR (60 min of ischemia followed by 24 hr of reperfusion), (c) zofenopril (15 mg/kg/day for 2 days), and (d) zofenopril+IR. All of the rats underwent right nephrectomy, and the rats in the IR and zofenopril+IR groups also underwent IR.then the left kidneys were removed for biochemical analyses and microscopic examination. There were no abnormalities in the biochemical and microscopic findings in the preoperative right kidneys. The lipid peroxidation, protein oxidation, and nitric oxide levels as well as xanthine oxidase and myeloperoxidase activities were increased and the catalase and superoxide dismutase activities were decreased in the IR group; zofenopril treatment prevented these changes (p <0.05). In the IR group, the kidney sections showed severe acute tubular damage including brush border loss, nuclear condensation, cytoplasmic swelling, and loss of nuclei; in the zofenopril+IR group, the normal glomerular morphology was preserved and there was slight edema of the tubular cells. The renal damage score was significantly reduced in the zofenopril+IR group vs the IR group (p <0.05).In conclusion, IR injury caused oxidative damage in renal tissue and zofenopril prevented this IR injury.

Keywords: zofenopril, kidney ischemia/reperfusion, oxidative stress, antioxidants







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the Association of Clinical Scientists.