An improved method for extracting myeloperoxidase and determining its activity in the pancreas and lungs during pancreatitis.

Objectives: This study was undertaken to examine the cause of variation in determined values of myeloperoxidase activity from sequestered neutrophils in pancreas and lungs during pancreatitis and to develop a reproducible method for the extraction and measurement of myeloperoxidase in these tissues.

Methods: We measured myeloperoxidase in pancreatic and lung homogenates at different steps and evaluated the extent of inhibitory activity by measuring enzyme activity in the presence of homogenates from normal lungs and pancreata. To remove inhibitory activity from the homogenates, different methods like heat inactivation, inclusion of catalase inhibitor, and membranous pellet washing were evaluated.

Heat shock protein 70 increases tumorigenicity and inhibits apoptosis in pancreatic adenocarcinoma.

Pancreatic carcinoma is a malignant disease that responds poorly to chemotherapy because of its resistance to apoptosis. Heat shock proteins (Hsp) are not only cytoprotective but also interfere with the apoptotic cascade. Here, we investigated the role of Hsp70 in regulating apoptosis in pancreatic cancer cells.

Development of a new mouse model of acute pancreatitis induced by administration of L-arginine.

The pathogenesis of acute pancreatitis is not fully understood. Experimental animal models that mimic human disease are essential to better understand the pathophysiology of the disease and to evaluate potential therapeutic agents. Given that the mouse genome is known completely and that a large number of strains with various genetic deletions are available, it is advantageous to have multiple reliable mouse models of acute pancreatitis.

Protease-activated receptor-2 protects against pancreatitis by stimulating exocrine secretion.

Background: Protease-activated receptor-2 (PAR-2) is present in the pancreas, where it has been shown to play a protective role during pancreatitis. However, the mechanism by which it protects against pancreatitis still remains to be elucidated. Acute pancreatitis is associated with premature zymogen activation and a blockage in digestive enzyme secretion.