dc.contributor.authorMerza, Mohammed
dc.contributor.authorRahman, Milladur
dc.contributor.authorZhang, Songen
dc.contributor.authorHwaiz, Rundk
dc.contributor.authorRegner, Sara
dc.contributor.authorSchmidtchen, Artur
dc.contributor.authorThorlacius, Henrik
dc.date.accessioned2015-02-12T03:37:34Z
dc.date.available2015-02-12T03:37:34Z
dc.date.copyright2014en_US
dc.date.issued2014
dc.identifier.citationMerza, M., Rahman, M., Zhang, S., Hwaiz, R., Regner, S., Schmidtchen, A., & Thorlacius, H. (2014). Human thrombin-derived host defense peptides inhibit neutrophil recruitment and tissue injury in severe acute pancreatitis. American journal of physiology - gastrointestinal and liver physiology , 307(9), G914-G921.en_US
dc.identifier.issn0193-1857en_US
dc.identifier.urihttp://hdl.handle.net/10220/25033
dc.description.abstractSevere acute pancreatitis (AP) is characterized by leukocyte infiltration and tissue injury. Herein, we wanted to examine the potential effects of thrombin-derived host defense peptides (TDPs) in severe AP. Pancreatitis was provoked by infusion of taurocholate into the pancreatic duct or by intraperitoneal administration of L-arginine in C57BL/6 mice. Animals were treated with the TDPs GKY20 and GKY25 or a control peptide WFF25 30 min before induction of AP. TDPs reduced blood amylase levels, neutrophil infiltration, hemorrhage, necrosis, and edema formation in the inflamed pancreas. Treatment with TDPs markedly attenuated the taurocholate-induced increase in plasma levels of CXCL2 and interleukin-6. Moreover, administration of TDPs decreased histone 3, histone 4, and myeloperoxidase levels in the pancreas in response to taurocholate challenge. Interestingly, administration of TDPs abolished neutrophil expression of Mac-1 in mice with pancreatitis. In addition, TDPs inhibited CXCL2-induced chemotaxis of isolated neutrophils in vitro. Fluorescent-labeled TDP was found to directly bind to isolated neutrophils. Finally, a beneficial effect of TDPs was confirmed in L-arginine-induced pancreatitis. Our novel results demonstrate that TDPs exert protective effects against pathological inflammation and tissue damage in AP. These findings suggest that TDPs might be useful in the management of patients with severe AP.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesAmerican journal of physiology - gastrointestinal and liver physiologyen_US
dc.rights© 2014 the American Physiological Society.en_US
dc.subjectDRNTU::Science::Biological sciences::Human anatomy and physiology
dc.titleHuman thrombin-derived host defense peptides inhibit neutrophil recruitment and tissue injury in severe acute pancreatitisen_US
dc.typeJournal Article
dc.contributor.schoolLee Kong Chian School of Medicine
dc.identifier.doihttp://dx.doi.org/10.1152/ajpgi.00237.2014


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