Pulmonary injuries and cytokine levels after the intraperitoneal administration of pancreatic homogenates in rats

• Published in: Revista española de enfermedades digestivas Vol. 96; no. 8; pp. 527 - 33; 533-8
• Main Authors: Mozo, G, del Olmo, M L, Caro-Patón, A, Reyes, E, Manzano, L, Belmonte, A, Almaraz, A, Alvarez-Mon, M
• Format: Journal Article
• Language: English
• Published: Spain Sociedad Española de Patología Digestiva 01-08-2004
• Subjects: Animals; Cytokines - blood; Enteropeptidase - administration & dosage; Gastroenterology & Hepatology; Geriatrics & Gerontology; Infectious Diseases; Interleukin-1 - blood; Lung - pathology; Lung Diseases - blood; Lung Diseases - etiology; Male; Oncology; Pancreas; Pathology; Peritoneum; Pharmacology & Pharmacy; Radiology, Nuclear Medicine & Medical Imaging; Rats; Rats, Wistar; Surgery; Tissue Extracts - administration & dosage; Pancreatic homogenates; Interleukin-1ß; Interleucina 1ß; Pulmón; Lung; Pancreatitis; TNFalpha; Pancreatic ascites; Páncreas; TNFalfa
• ISSN: 1130-0108; 1130-0108
• DOI: 10.4321/S1130-01082004000800002

Our objective was to investigate the effects of the administration of pancreatic homogenates, with or without enzymatic activation, to healthy animals regarding cytokine serum levels and the development of pulmonary distress.
106 male Wistar rats, divided into three groups, were studied: group A, intraperitoneal administration of homogenates activated with enterokinase; group B, homogenates without enterokinase; and group C, control group with administration of physiological saline solution. Each group was divided into 4 subgroups according to the time of sacrifice: 0, 2, 6 and 24 hours. We studied the pulmonary and pancreatic histology, serum parameters of renal and hepatic function, and serum levels of IL-1beta, IL-6 and TNFalpha.
There was no mortality in any group. Pancreatic disorders in A and B groups were noted at 24 hours. These two groups had statistically significant higher transaminase serum levels than those of the control group, as well as statistically significant higher creatinine levels in group A. IL-1beta showed a statistically significant higher level at 6 h in both groups, A and B, but was higher in group A, which also exhibited significant pulmonary histologic damage with respect to controls at 6 h.
The higher IL-1beta level in group A may result from production by peritoneal macrophages under the influence of homogenate enzymatic activation. This may be the reason for lung damage.