Literature DB >> 21911117

Lisinopril inhibits endothelin-1 in the early period of hepatic reperfusion injury in a partial hepatectomy model.

O A Yirmibeşoğlu1, O Büyükgebiz, D Ars, O Unay, D Cevik.   

Abstract

BACKGROUND: Ischemia-reperfusion (I/R) injury is a major problem during liver surgery. We investigated the effects of lisinopril, an angiotensin-converting enzyme inhibitor, in the early postoperative period of reperfusion injury after Pringle's maneuver during an 80% partial hepatectomy (PH) in rats.
METHODS: Four groups of male Sprague-Dawley rats were studied: Group 1 (n = 10), sham laparotomy; group 2 (n = 10), PH without portal occlusion; group 3 (n = 10), PH with portal pedicle clamping; group 4 (n = 15), same as group 3 with additional intravenous lisinopril preconditioning (1 mg/kg(-1)). We analyzed superoxide radical (O(2)(-)), nitric oxide (NO), peroxynitrite (ONOO(-)) levels in the liver tissue and blood levels of alanine aminotransferase (ALT) and endothelin-1 (ET-1).
RESULTS: ALT and ET-1 levels were progressively increased in group 2 (P > .05) versus group 3 (P < .001 and P < .05), showing hepatocellular damage due to I/R injury in the remnant liver, although histopathologic changes were unremarkable at this early stage. The levels of ALT and ET-1 decreased with lisinopril precontioning in group 4 compared with group 2 (P > .05 and P < .01) or group 3 (P < .05 and P < .001). O(2)(-) levels were increased significantly in groups 2 and 3 (P < .01 for both). O(2)(-) level in Group 4 was remarkably decreased albeit not significant compared with the other groups. NO and ONOO(-) levels were also significantly greater in groups 2 (P < .01 and P < .05) and 3 (P < .001 and P < .01). These levels were decreased significantly among group 4 compared with group 3 (P < .05), a decline almost to the level of group 1 (P > .05).
CONCLUSION: In the early postoperative period of an extended hepatectomy model, Pringle's maneuver causes I/R increasing the insult to the remnant liver. Lisinopril preconditioning alleviated I/R injury by decreasing the O(2)(-), NO, ONOO(-), ET-1, and ALT levels, thereby exerting a protective role on the remaining liver.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21911117     DOI: 10.1016/j.transproceed.2011.06.043

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  2 in total

1.  Effect of amlodipine, lisinopril and allopurinol on acetaminophen-induced hepatotoxicity in rats.

Authors:  Nesreen E M Mohammed; Basim A S Messiha; Ali A Abo-Saif
Journal:  Saudi Pharm J       Date:  2015-05-19       Impact factor: 4.330

2.  Study of the protective effect of ischemic and pharmacological preconditioning on hepatic ischemic reperfusion injury induced in rats.

Authors:  Afaf S Osman; Ahmed H Osman; Mahmoud M Kamel
Journal:  JGH Open       Date:  2017-11-14
  2 in total

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