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Role of angiotensin and endothelin in testicular ischemia reperfusion injury

Objectives:  To determine whether angiotensin and endothelin have any role in testicular ischemia reperfusion injury by investigating the effects of the angiotensin converting enzyme inhibitor enalapril, selective non‐peptide angiotensin‐II type I blocker losartan and dual endothelin receptor blocke...

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Bibliographic Details
Published in:International journal of urology 2012-03, Vol.19 (3), p.257-263
Main Authors: Turkili, Burak, Kurcer, Zehra, Dengiz, Gunnur Ozbakis, Kandemir, Nilufer Onak, Mungan, Gorkem, Ozacmak, Veysel Haktan, Banoglu, Zekiye Nur
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Language:English
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Summary:Objectives:  To determine whether angiotensin and endothelin have any role in testicular ischemia reperfusion injury by investigating the effects of the angiotensin converting enzyme inhibitor enalapril, selective non‐peptide angiotensin‐II type I blocker losartan and dual endothelin receptor blocker bosentan. Methods:  Rats were anesthetized with thiopental sodium (50 mg/kg i.p.) before the operation. The left testicular artery and vein of rats were occluded for 1 h; before the bilateral orchiectomy, the organ was allowed to reperfuse for 3 h or 24 h. Enalapril (20 mg/kg i.p.), losartan (30 mg/kg i.p.), bosentan (10 mg/kg i.p.) or vehicle (saline) were given 30 min before reperfusion. Malondialdehyde level was measured in testicular tissue after 3 h of reperfusion. Histological examination was carried out after 24 h of reperfusion. Results:  Ischemia reperfusion caused a significant increase in malondialdehyde level of ipsilateral testis, and histopathological injury in both ipsilateral and contralateral testes. Enalapril, losartan and bosentan treatments prevented the ischemia reperfusion‐induced augmentation in malondialdehyde levels. Only bosentan treatment ameloriated ischemia reperfusion‐induced histopathological alterations. Conclusions:  Endothelin might play a more important role in pathogenesis of testicular ischemia reperfusion injury when compared with angiotensin.
ISSN:0919-8172
1442-2042
DOI:10.1111/j.1442-2042.2011.02924.x