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Mice deficient in pituitary adenylate cyclase activating polypeptide (PACAP) show increased susceptibility to in vivo renal ischemia/reperfusion injury.

Authors :
Szakaly, Peter
Laszlo, Eszter
Kovacs, Krisztina
Racz, Boglarka
Horvath, Gabriella
Ferencz, Andrea
Lubics, Andrea
Kiss, Peter
Tamas, Andrea
Brubel, Reka
Opper, Balazs
Baba, Akemichi
Hashimoto, Hitoshi
Farkas, Jozsef
Matkovits, Attila
Magyarlaki, Tamas
Helyes, Zsuzsanna
Reglodi, Dora
Source :
Neuropeptides; Apr2011, Vol. 45 Issue 2, p113-121, 9p
Publication Year :
2011

Abstract

Abstract: Pituitary adenylate cyclase activating polypeptide (PACAP) is a neuropeptide with well-known cytoprotective effects. We have reported earlier that PACAP decreases mortality and the degree of tubular atrophy in a rat model of renal ischemia/reperfusion injury. Recently, we have shown that kidney cultures isolated from PACAP deficient mice show increased susceptibility to renal oxidative stress. Based on these previous studies, we raised the question whether PACAP deficient mice display increased sensitivity to in vivo kidney ischemia/reperfusion. PACAP<superscript>−/−</superscript> mice underwent 45 or 60min of renal ischemia followed by 2weeks reperfusion. Kidneys were processed for histological analysis. Sections stained with PAS–haematoxylin were graded for the following parameters: degree of tubular dilation, Bowmann’s capsule dilation, lymphocyte and macrophage infiltration, thyroidization and the disappearance of the PAS-positive glycocalyx from under the brush border. In other sets of experiments, tissue cytokine expression and the level of the endogenous antioxidant superoxide dismutase (SOD) were also determined after 60min ischemia/reperfusion. Our results show that while intact kidneys were not different between wild-type and PACAP deficient mice, marked differences were observed in the histological structures in groups that underwent ischemia/reperfusion. PACAP deficient mice had a worse histological outcome, with significantly higher histological scores for all tested parameters. Cytokine expression was also markedly different between wild-type and PACAP deficient mice. In addition, the level of SOD was significantly lower in PACAP<superscript>−/−</superscript> animals after ischemia/reperfusion. In conclusion, the lack of endogenous PACAP leads to higher susceptibility to in vivo renal ischemia/reperfusion, suggesting that PACAP has an endogenous renoprotective effect. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01434179
Volume :
45
Issue :
2
Database :
Supplemental Index
Journal :
Neuropeptides
Publication Type :
Academic Journal
Accession number :
58101662
Full Text :
https://doi.org/10.1016/j.npep.2010.12.003