Literature DB >> 18435717

Effect of adrenomedullin on hepatic damage in hepatic ischaemia/reperfusion injury in rats.

Mustafa Kerem1, Abdulkadir Bedirli, Hatice Pasaoglu, Ebru Ofluoğlu, Demet Yilmazer, Bulent Salman, Tonguc Utku Yilmaz.   

Abstract

AIMS: Adrenomedullin (AM) is a multifunctional peptide with a putative beneficial role after an ischaemic insult. The aim of this study was to evaluate the effect of AM on partial hepatic ischaemia reperfusion (I/R) injury.
METHODS: Rats were subjected to 1 h of 70% hepatic ischaemia, followed by reperfusion or sham. At the end of ischaemia, vehicle (phosphate-buffered saline solution), N-nitro-L-arginine methyl ester (L-NAME) and AM with or without L-NAME were infused via the portal vein. Analysis was performed at pre-ischaemia, ischaemia onset and 1, 2 and 4 h after reperfusion. Hepatic tissue blood flow (HTBF) was evaluated by laser Doppler.
RESULTS: Plasma AM levels in the I/R groups were significantly lower than the levels in the sham group. AM treatment significantly reduced levels of aspartate transaminase and tissue arginase (P<0.05). Significant decreases of tumour necrosis factor-alpha, interleukin-1beta and endothelin-1 levels were also found in the serum. Endothelin-1, malondialdehyde and necrosis were observed more frequently in liver tissue in the AM group than the control (P<0.05). Tissue nitric oxide, energy charge and HTBF were significantly increased in AM treatment experiments (P<0.05).
CONCLUSION: The improved HTBF, energy charge and nitric oxide and the reduction of hepatic necrosis, oxidative stress, liver enzymes, endotelin-1 and pro-inflammatory cytokines demonstrate that treatment with AM attenuates liver I/R injury.

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Year:  2008        PMID: 18435717     DOI: 10.1111/j.1478-3231.2008.01741.x

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  1 in total

Review 1.  Arginase induction and activation during ischemia and reperfusion and functional consequences for the heart.

Authors:  Klaus-Dieter Schlüter; Rainer Schulz; Rolf Schreckenberg
Journal:  Front Physiol       Date:  2015-03-11       Impact factor: 4.566

  1 in total

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