Journal
NEPHRON EXPERIMENTAL NEPHROLOGY
Volume 112, Issue 1, Pages E10-E19Publisher
KARGER
DOI: 10.1159/000210574
Keywords
Ischemia-reperfusion injury; AT1 blockade; Inflammation; Aldosterone
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Funding
- Consejo Nacional de Investigaciones Cientificas y Tecnologicas, Argentina [CONICET PIP 06039]
- Consejo Nacional de Ciencias y Tecnologia de Mexico [CONACYT 48483]
- National University of Mexico [PAPIIT 228206-3]
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Background/Aims: Contributions to the understanding of acute renal failure (ARF) pathogenesis have not been translated into an effective clinical therapy. We studied the effects of pretreatment with the angiotensin II type 1 (AT1) receptor blocker, losartan, on renal function, tissue injury, inflammatory response and serum aldosterone levels in a model of ischemic ARF. Methods: Rats underwent unilateral renal ischemia followed by 24 h of reperfusion (IR), and were pretreated or not with 8 (IRL8) or 80 (IRL80) mg/kg/day of losartan for 3 days. Results: IR kidneys showed marked renal dysfunction, epithelial damage, capillary congestion, increased myeloperoxidase (MPO) activity and increased TNF-alpha, IL1-beta and IL-6 mRNA levels. IRL80 kidneys showed protection against dysfunction and tissue injury, associated with normal MPO activity and cytokine mRNA levels. The lower dose was not able to achieve the same degree of functional renoprotection and could not prevent an increase of MPO or pro-inflammatory cytokine mRNA levels. The high losartan dose completely prevented an increase of serum aldosterone levels induced by IR. Conclusion: Renoprotection of the high losartan dose would be mainly mediated by its anti-inflammatory actions. Our results show a potential pathophysiological role of AT1 activation in promoting renal dysfunction, structural injury, inflammation and aldosterone elevation after IR injury. Copyright (C) 2009 S. Karger AG, Basel
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