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Anti-CD163-dexamethasone protects against apoptosis after ischemia/reperfusion injuries in the rat liver

Authors :
Kasper Jarlhelt Andersen
Anders Riegels Knudsen
Jens R. Nyengaard
Pia Svendsen
Jonas Heilskov Graversen
Søren K. Moestrup
Frank Viborg Mortensen
Stephen Hamilton-Dutoit
Lin Nanna Okholm Møller
Holger Jon Møller
Elise Marie Okholm Møller
Source :
Møller, L N O, Knudsen, A R, Andersen, K J, Nyengaard, J R, Hamilton-Dutoit, S, Okholm Møller, E M, Svendsen, P, Møller, H J, Moestrup, S K, Graversen, J H & Mortensen, F V 2015, ' Anti-CD163-dexamethasone protects against apoptosis after ischemia/reperfusion injuries in the rat liver ', Annals of Medicine and Surgery, vol. 4, no. 4, 130, pp. 331-337 . https://doi.org/10.1016/j.amsu.2015.09.001, Annals of Medicine and Surgery, Møller, L N O, Knudsen, A R, Andersen, K J, Nyengaard, J R, Hamilton-Dutoit, S, Okholm Møller, E M, Svendsen, P, Møller, H J, Moestrup, S K, Graversen, J H & Mortensen, F V 2015, ' Anti-CD163-dexamethasone protects against apoptosis after ischemia/reperfusion injuries in the rat liver ', Annals of Medicine and Surgery, vol. 4, no. 4, pp. 331-337 . https://doi.org/10.1016/j.amsu.2015.09.001
Publication Year :
2015
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2015.

Abstract

Aim The Pringle maneuver is a way to reduce blood loss during liver surgery. However, this may result in ischemia/reperfusion injury in the development of which Kupffer cells play a central role. Corticosteroids are known to have anti-inflammatory effects. Our aim was to investigate whether a conjugate of dexamethasone and antibody against the CD163 macrophage cell surface receptor could reduce ischemia/reperfusion injury in the rat liver. Methods Thirty-six male Wistar rats were used for the experiments. Animals were randomly divided into four groups of eight receiving anti-CD163-dexamethasone, high dose dexamethasone, low dose dexamethasone or placebo intravenously 18 h before laparotomy with subsequent 60 min of liver ischemia. After reperfusion for 24 h the animals had their liver removed. Bloods were drawn 30 min and 24 h post ischemia induction. Liver cell apoptosis and necrosis were analyzed by stereological quantification. Results After 24 h' reperfusion, the fraction of cell in non-necrotic tissues exhibiting apoptotic profiles was significantly lower in the high dose dexamethasone (p = 0.03) and anti-CD163-dex (p = 0.03) groups compared with the low dose dexamethasone and placebo groups. There was no difference in necrotic cell volume between groups. After 30 min of reperfusion, levels of haptoglobin were significantly higher in the anti-CD163-dex and high dose dexamethasone groups. Alanine aminotransferase and alkaline phosphatase were significantly higher in the high dose dexamethasone group compared to controls after 24 h' reperfusion. Conclusions We show that pharmacological preconditioning with anti-CD163-dex and high dose dexamethasone reduces the number of apoptotic cells following ischemia/reperfusion injury.<br />Highlights • We investigated the effect of pharmacologic preconditioning with HDD, LDD and anti-CD163-dex on ischemia/reperfusion injury. • Liver cell apoptosis and necrosis were analyzed by stereological quantification. • Anti-CD163-dex and high dose dexamethasone reduces the number of apoptotic cells following ischemia/reperfusion injury.

Details

ISSN :
20490801
Volume :
4
Database :
OpenAIRE
Journal :
Annals of Medicine & Surgery
Accession number :
edsair.doi.dedup.....2152cd2f1e7a50822acf0aa490951115
Full Text :
https://doi.org/10.1016/j.amsu.2015.09.001