Determining the Pancreatic Arginase Activity and a-Amylase Levels in Patients with Type 2 Diabetes and Alcoholic Pancreatitis

Méndez, José D. and Haro, Roberto De and Méndez-Valenzuela, Verna and Ble-Castillo, Jorge L. and Rubio, Hector O. (2021) Determining the Pancreatic Arginase Activity and a-Amylase Levels in Patients with Type 2 Diabetes and Alcoholic Pancreatitis. In: Challenging Issues on Environment and Earth Science Vol. 5. B P International, pp. 12-20. ISBN 978-93-91312-22-0

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Abstract

Arginase, a regenerative enzyme located in the endocrine pancreas, is involved in insulin metabolism and regenerative processes during polyamine formation. Pancreatic damage has been linked to high levels of -amylase. The aim of this study was to determine the function of arginase and -amylase in the pancreas of people with type 2 diabetes and those who had alcohol-induced acute pancreatitis. Patients with type 2 diabetes mellitus or acute pancreatitis without pancreatic diabetes had their arginase and -amylase activities assessed in pancreatic tissue. The findings were compared to the results of a control group. Our findings indicate that diabetics' pancreas have higher arginase activity than controls, while pancreatitis patients' tissues have lower arginase activity (P <0.05). The activity of a-amylase was higher in type 2 diabetes patients' pancreases than in acute pancreatitis patients' pancreases. Rather than being the source of damage mediators, elevated arginase activity in type 2 diabetes patients may be linked to an effort to reclaim endocrine pancreatic function. Because there is acinar damage in pancreatitis with a subsequent release a -amylase, this enzyme was higher in pancreatic tissue of diabetics than in pancreatic tissue of pancreatitis patients.

Item Type: Book Section
Subjects: Research Scholar Guardian > Geological Science
Depositing User: Unnamed user with email support@scholarguardian.com
Date Deposited: 28 Nov 2023 03:52
Last Modified: 28 Nov 2023 03:52
URI: http://science.sdpublishers.org/id/eprint/1894

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