Zofenopril attenuates injury induced by ischemia-reperfusion on rat ovary

Aim The aim of the study was to investigate the effectiveness of zofenopril in an experimental model of ovarian torsion in rats with histologic and biochemical assessments. Material and Methods Experimental procedures were performed on 35 female rats (Wistar albino). Rats were randomly divided into...

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Veröffentlicht in:The journal of obstetrics and gynaecology research 2015-06, Vol.41 (6), p.926-931
Hauptverfasser: Keskin Kurt, Raziye, Dogan, Ayşe Citil, Dogan, Murat, Albayrak, Aynur, Kurt, Sefika Nur, Eren, Furkan, Silfeler, Dilek Benk, Karateke, Atilla, Fadillioglu, Ersin, Delibasi, Tuncay
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container_issue 6
container_start_page 926
container_title The journal of obstetrics and gynaecology research
container_volume 41
creator Keskin Kurt, Raziye
Dogan, Ayşe Citil
Dogan, Murat
Albayrak, Aynur
Kurt, Sefika Nur
Eren, Furkan
Silfeler, Dilek Benk
Karateke, Atilla
Fadillioglu, Ersin
Delibasi, Tuncay
description Aim The aim of the study was to investigate the effectiveness of zofenopril in an experimental model of ovarian torsion in rats with histologic and biochemical assessments. Material and Methods Experimental procedures were performed on 35 female rats (Wistar albino). Rats were randomly divided into five groups as: sham (sham operated, n = 7); vehicle group 1 (torsion–detorsion, n = 7) with 2 h ischemia and 2 h reperfusion; vehicle group 2 (torsion–detorsion, n = 7) with 2 h ischemia and 5 days' reperfusion; zofenopril group 1 (torsion–detorsion, n = 7) with 2 h ischemia, 2 h reperfusion and a signal dose of oral 15 mg/kg zofenopril; and zofenopril group 2 (torsion–detorsion, n = 7) with 2 h ischemia, 5 days' reperfusion and 5 days' oral 15 mg/kg zofenopril. A scoring of histopathologic evaluation was performed on the ovaries according to congestion, bleeding, edema, and cellular degeneration. Biochemical assessments included catalase, tissue malondialdehyde and protein carbonyl. Results Compared with the vehicle groups, histopathologic scores, tissue malondialdehyde and protein carbonyl levels, which reflect oxidative stress markers, were significantly lower in the zofenopril groups. Furthermore, catalase levels were significantly increased in the zofenopril group. Conclusion Our study results revealed that zofenopril attenuates injury induced by ischemia‐reperfusion on rat ovary.
doi_str_mv 10.1111/jog.12658
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Material and Methods Experimental procedures were performed on 35 female rats (Wistar albino). Rats were randomly divided into five groups as: sham (sham operated, n = 7); vehicle group 1 (torsion–detorsion, n = 7) with 2 h ischemia and 2 h reperfusion; vehicle group 2 (torsion–detorsion, n = 7) with 2 h ischemia and 5 days' reperfusion; zofenopril group 1 (torsion–detorsion, n = 7) with 2 h ischemia, 2 h reperfusion and a signal dose of oral 15 mg/kg zofenopril; and zofenopril group 2 (torsion–detorsion, n = 7) with 2 h ischemia, 5 days' reperfusion and 5 days' oral 15 mg/kg zofenopril. A scoring of histopathologic evaluation was performed on the ovaries according to congestion, bleeding, edema, and cellular degeneration. Biochemical assessments included catalase, tissue malondialdehyde and protein carbonyl. Results Compared with the vehicle groups, histopathologic scores, tissue malondialdehyde and protein carbonyl levels, which reflect oxidative stress markers, were significantly lower in the zofenopril groups. Furthermore, catalase levels were significantly increased in the zofenopril group. Conclusion Our study results revealed that zofenopril attenuates injury induced by ischemia‐reperfusion on rat ovary.</description><identifier>ISSN: 1341-8076</identifier><identifier>EISSN: 1447-0756</identifier><identifier>DOI: 10.1111/jog.12658</identifier><identifier>PMID: 25546378</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject><![CDATA[Angiotensin-Converting Enzyme Inhibitors - administration & dosage ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Animals ; antioxidant ; Antioxidants - administration & dosage ; Antioxidants - therapeutic use ; Biomarkers - metabolism ; Captopril - administration & dosage ; Captopril - analogs & derivatives ; Captopril - therapeutic use ; Catalase - antagonists & inhibitors ; Catalase - metabolism ; Dose-Response Relationship, Drug ; Female ; ischemia-reperfusion injury ; Malondialdehyde - antagonists & inhibitors ; Malondialdehyde - metabolism ; Ovarian Diseases - etiology ; Ovarian Diseases - metabolism ; Ovarian Diseases - pathology ; Ovarian Diseases - prevention & control ; ovarian torsion ; Ovary - blood supply ; Ovary - drug effects ; Ovary - metabolism ; Ovary - pathology ; Oxidative Stress - drug effects ; Protein Carbonylation - drug effects ; Random Allocation ; Rats, Wistar ; Reperfusion Injury - etiology ; Reperfusion Injury - metabolism ; Reperfusion Injury - pathology ; Reperfusion Injury - prevention & control ; Torsion, Mechanical ; zofenopril]]></subject><ispartof>The journal of obstetrics and gynaecology research, 2015-06, Vol.41 (6), p.926-931</ispartof><rights>2014 The Authors. Journal of Obstetrics and Gynaecology Research © 2014 Japan Society of Obstetrics and Gynecology</rights><rights>2014 The Authors. Journal of Obstetrics and Gynaecology Research © 2014 Japan Society of Obstetrics and Gynecology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3878-3f134b18bd9e3ebbee30a1150e5b6c1f2c95492ffc9b250fdf5be0dd339743983</citedby><cites>FETCH-LOGICAL-c3878-3f134b18bd9e3ebbee30a1150e5b6c1f2c95492ffc9b250fdf5be0dd339743983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjog.12658$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjog.12658$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27933,27934,45583,45584</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25546378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Keskin Kurt, Raziye</creatorcontrib><creatorcontrib>Dogan, Ayşe Citil</creatorcontrib><creatorcontrib>Dogan, Murat</creatorcontrib><creatorcontrib>Albayrak, Aynur</creatorcontrib><creatorcontrib>Kurt, Sefika Nur</creatorcontrib><creatorcontrib>Eren, Furkan</creatorcontrib><creatorcontrib>Silfeler, Dilek Benk</creatorcontrib><creatorcontrib>Karateke, Atilla</creatorcontrib><creatorcontrib>Fadillioglu, Ersin</creatorcontrib><creatorcontrib>Delibasi, Tuncay</creatorcontrib><title>Zofenopril attenuates injury induced by ischemia-reperfusion on rat ovary</title><title>The journal of obstetrics and gynaecology research</title><addtitle>J Obstet Gynaecol Res</addtitle><description>Aim The aim of the study was to investigate the effectiveness of zofenopril in an experimental model of ovarian torsion in rats with histologic and biochemical assessments. Material and Methods Experimental procedures were performed on 35 female rats (Wistar albino). Rats were randomly divided into five groups as: sham (sham operated, n = 7); vehicle group 1 (torsion–detorsion, n = 7) with 2 h ischemia and 2 h reperfusion; vehicle group 2 (torsion–detorsion, n = 7) with 2 h ischemia and 5 days' reperfusion; zofenopril group 1 (torsion–detorsion, n = 7) with 2 h ischemia, 2 h reperfusion and a signal dose of oral 15 mg/kg zofenopril; and zofenopril group 2 (torsion–detorsion, n = 7) with 2 h ischemia, 5 days' reperfusion and 5 days' oral 15 mg/kg zofenopril. A scoring of histopathologic evaluation was performed on the ovaries according to congestion, bleeding, edema, and cellular degeneration. Biochemical assessments included catalase, tissue malondialdehyde and protein carbonyl. Results Compared with the vehicle groups, histopathologic scores, tissue malondialdehyde and protein carbonyl levels, which reflect oxidative stress markers, were significantly lower in the zofenopril groups. Furthermore, catalase levels were significantly increased in the zofenopril group. 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Material and Methods Experimental procedures were performed on 35 female rats (Wistar albino). Rats were randomly divided into five groups as: sham (sham operated, n = 7); vehicle group 1 (torsion–detorsion, n = 7) with 2 h ischemia and 2 h reperfusion; vehicle group 2 (torsion–detorsion, n = 7) with 2 h ischemia and 5 days' reperfusion; zofenopril group 1 (torsion–detorsion, n = 7) with 2 h ischemia, 2 h reperfusion and a signal dose of oral 15 mg/kg zofenopril; and zofenopril group 2 (torsion–detorsion, n = 7) with 2 h ischemia, 5 days' reperfusion and 5 days' oral 15 mg/kg zofenopril. A scoring of histopathologic evaluation was performed on the ovaries according to congestion, bleeding, edema, and cellular degeneration. Biochemical assessments included catalase, tissue malondialdehyde and protein carbonyl. Results Compared with the vehicle groups, histopathologic scores, tissue malondialdehyde and protein carbonyl levels, which reflect oxidative stress markers, were significantly lower in the zofenopril groups. Furthermore, catalase levels were significantly increased in the zofenopril group. Conclusion Our study results revealed that zofenopril attenuates injury induced by ischemia‐reperfusion on rat ovary.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>25546378</pmid><doi>10.1111/jog.12658</doi><tpages>6</tpages></addata></record>
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subjects Angiotensin-Converting Enzyme Inhibitors - administration & dosage
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Animals
antioxidant
Antioxidants - administration & dosage
Antioxidants - therapeutic use
Biomarkers - metabolism
Captopril - administration & dosage
Captopril - analogs & derivatives
Captopril - therapeutic use
Catalase - antagonists & inhibitors
Catalase - metabolism
Dose-Response Relationship, Drug
Female
ischemia-reperfusion injury
Malondialdehyde - antagonists & inhibitors
Malondialdehyde - metabolism
Ovarian Diseases - etiology
Ovarian Diseases - metabolism
Ovarian Diseases - pathology
Ovarian Diseases - prevention & control
ovarian torsion
Ovary - blood supply
Ovary - drug effects
Ovary - metabolism
Ovary - pathology
Oxidative Stress - drug effects
Protein Carbonylation - drug effects
Random Allocation
Rats, Wistar
Reperfusion Injury - etiology
Reperfusion Injury - metabolism
Reperfusion Injury - pathology
Reperfusion Injury - prevention & control
Torsion, Mechanical
zofenopril
title Zofenopril attenuates injury induced by ischemia-reperfusion on rat ovary
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