Acute pancreatitis in aging animals: Loss of pancreatitis- associated protein protection

AIM:To investigate the effect of age on severity of acute pancreatitis(AP) using biochemical markers,histology and expression of the protective pancreatitisassociated proteins(PAPs).METHODS:AP was induced via intraductal injection of 4% sodium taurocholate in young and old rats.Sera and pancreata we...

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Published inWorld journal of gastroenterology : WJG Vol. 18; no. 26; pp. 3379 - 3388
Main Authors Fu, Sophia, Stanek, Albert, Mueller, Cathy M, Brown, Nefertti A, Huan, Chongmin, Bluth, Martin H, Zenilman, Michael E
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Co., Limited 14.07.2012
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Summary:AIM:To investigate the effect of age on severity of acute pancreatitis(AP) using biochemical markers,histology and expression of the protective pancreatitisassociated proteins(PAPs).METHODS:AP was induced via intraductal injection of 4% sodium taurocholate in young and old rats.Sera and pancreata were assayed at 24 h for the parameters listed above;we also employed a novel molecular technique to assess bacterial infiltration using polymerase chain reaction to measure bacterial genomic ribosomal RNA.RESULTS:At 24 h after induction of AP,the pancreata of older animals had less edema(mean ± SE histologic score of young vs old:3.11 ± 0.16 vs 2.50 ±-0.11,P 〈 0.05),decreased local inflammatory response(histologic score of stromal infiltrate:3.11 ± 0.27 vs 2.00 ± 0.17,P 〈 0.05) and increased bacterial infiltration(174% ± 52% increase from sham vs 377% ± 4%,P 〈 0.05).A decreased expression of PAP1 and PAP2 was demonstrated by Western blotting analysis and immunohistochemical staining.There were no differences in serum amylase and lipase activity,or tissue myeloperoxidase or monocyte chemotactic protein-1 levels.However,in the most-aged group,serum C-reactive protein levels were higher(young vs old:0.249 ± 0.04 mg/dL vs 2.45 ± 0.68 mg/dL,P 〈 0.05).CONCLUSION:In older animals,there is depressed PAP expression related to a blunted inflammatory response in AP which is associated with worsened bacterial infiltration and higher C-reactive protein level;this may explain the more aggressive clinical course.
Bibliography:14-1219/R
AIM:To investigate the effect of age on severity of acute pancreatitis(AP) using biochemical markers,histology and expression of the protective pancreatitisassociated proteins(PAPs).METHODS:AP was induced via intraductal injection of 4% sodium taurocholate in young and old rats.Sera and pancreata were assayed at 24 h for the parameters listed above;we also employed a novel molecular technique to assess bacterial infiltration using polymerase chain reaction to measure bacterial genomic ribosomal RNA.RESULTS:At 24 h after induction of AP,the pancreata of older animals had less edema(mean ± SE histologic score of young vs old:3.11 ± 0.16 vs 2.50 ±-0.11,P 〈 0.05),decreased local inflammatory response(histologic score of stromal infiltrate:3.11 ± 0.27 vs 2.00 ± 0.17,P 〈 0.05) and increased bacterial infiltration(174% ± 52% increase from sham vs 377% ± 4%,P 〈 0.05).A decreased expression of PAP1 and PAP2 was demonstrated by Western blotting analysis and immunohistochemical staining.There were no differences in serum amylase and lipase activity,or tissue myeloperoxidase or monocyte chemotactic protein-1 levels.However,in the most-aged group,serum C-reactive protein levels were higher(young vs old:0.249 ± 0.04 mg/dL vs 2.45 ± 0.68 mg/dL,P 〈 0.05).CONCLUSION:In older animals,there is depressed PAP expression related to a blunted inflammatory response in AP which is associated with worsened bacterial infiltration and higher C-reactive protein level;this may explain the more aggressive clinical course.
Acute pancreatitis; Aging; Rats; Pancreati-tis-associated protein; Molecular biology
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Telephone: +1-301-8963509 Fax: +1-301-8971330
Author contributions: Fu S and Stanek A contributed equally; Huan C, Bluth MH and Zenilman ME designed research; Fu S, Stanek A, Mueller CM and Brown NA performed research; Fu S, Stanek A and Zenilman ME analyzed data; Fu S and Zenilman ME wrote the paper.
Correspondence to: Michael E Zenilman, MD, Department of Surgery, Johns Hopkins School of Medicine and SUNY Downstate School of Public Health, 8600 Old Georgetown Road, Bethesda, MD 20814, United States. mzenilm1@jhmi.edu
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v18.i26.3379