Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/106667
Title: Human thrombin-derived host defense peptides inhibit neutrophil recruitment and tissue injury in severe acute pancreatitis
Authors: Merza, Mohammed
Rahman, Milladur
Zhang, Songen
Hwaiz, Rundk
Regner, Sara
Schmidtchen, Artur
Thorlacius, Henrik
Keywords: DRNTU::Science::Biological sciences::Human anatomy and physiology
Issue Date: 2014
Source: Merza, 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.
Series/Report no.: American journal of physiology - gastrointestinal and liver physiology
Abstract: Severe 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.
URI: https://hdl.handle.net/10356/106667
http://hdl.handle.net/10220/25033
ISSN: 0193-1857
DOI: 10.1152/ajpgi.00237.2014
Rights: © 2014 the American Physiological Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:LKCMedicine Journal Articles

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