Characterization of the acute pancreatitis induced by secretory phospholipases A2 in rats

被引:21
作者
Camargo, EA
Esquisatto, LCM
Esquisatto, MA
Ribela, MTCP
Cintra, AC
Giglio, JR
Antunes, E
Landucci, ECT
机构
[1] State Univ Campinas UNICAMP, Fac Med Sci, Dept Pharmacol, BR-13084971 Campinas, SP, Brazil
[2] Univ Ctr Herminio Ometto, Araras, SP, Brazil
[3] CNEN, IPEN, Dept Biotechnol, Sao Paulo, Brazil
[4] Univ Sao Paulo, Fac Pharmaceut Sci Ribeirao Preto SP, Sao Paulo, Brazil
[5] State Univ Campinas UNICAMP, Inst Biol, Dept Biochem, BR-13084971 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
phospholipases A(2); acute pancreatitis; catalytic activity; sodium taurocholate;
D O I
10.1016/j.toxicon.2005.09.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acute pancreatitis (AP) is an inflammatory disease of the pancreas characterized by local inflammation and extrapancreatic effects such as lung injury. Secretory phospholipases A(2) (PLA(2)s) have been implicated in triggering AP, but their exact role to evoke AP is largely unknown. Therefore, we have tested the ability of sPLA(2)s to induce AP in rats, using venom sPLA(2)s with residual or high enzymatic activity (bothropstoxin-II and Naja mocambique mocambique venom PLA(2), respectively), as well as sPLA(2) devoid of catalytic activity (piratoxin-I). The injection of Naja m. mocambique venom PLA(2), bothropstoxin-II or piratoxin-I (300 mu g/kg each) into the common bile duct increased significantly the pancreatic plasma extravasation and myeloperoxidase activity. The lung myeloperoxidase and serum amylase were also increased for all groups, although the Naja mocambique mocambique venom PLA(2) induced higher lung myeloperoxidase and serum amylase values, compared with piratoxin-I and/or bothropstoxin-II. Histopathology of pancreas and lungs in piratoxin-I-injected rats showed interstitial oedema in both tissues, and neutrophil infiltration with acinar cell necrosis in pancreas. In conclusion, sPLA(2)s induce AP in rats and the catalytic activity is not essential to induce the local effects in pancreas, although it appears to contribute partly to the remote lung injury. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:921 / 926
页数:6
相关论文
共 35 条
[1]   EXPERIMENTAL PANCREATITIS IN THE RAT - SODIUM TAUROCHOLATE-INDUCED ACUTE HEMORRHAGIC-PANCREATITIS [J].
AHO, HJ ;
KOSKENSALO, SML ;
NEVALAINEN, TJ .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1980, 15 (04) :411-416
[2]   Regulation and inhibition of phospholipase A2 [J].
Balsinde, J ;
Balboa, MA ;
Insel, PA ;
Dennis, EA .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1999, 39 :175-189
[3]  
Bhatia M, 2000, J PATHOL, V190, P117
[4]  
Bhatia M., 2002, Current Drug Targets - Inflammation and Allergy, V1, P343
[5]   MEASUREMENT OF CUTANEOUS INFLAMMATION - ESTIMATION OF NEUTROPHIL CONTENT WITH AN ENZYME MARKER [J].
BRADLEY, PP ;
PRIEBAT, DA ;
CHRISTENSEN, RD ;
ROTHSTEIN, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 78 (03) :206-209
[6]   INFLAMMATORY EDEMA INDUCED BY SYNERGISM BETWEEN CALCITONIN GENE-RELATED PEPTIDE (CGRP) AND MEDIATORS OF INCREASED VASCULAR-PERMEABILITY [J].
BRAIN, SD ;
WILLIAMS, TJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1985, 86 (04) :855-860
[7]   SERUM PHOSPHOLIPASE-A2 IN INTENSIVE-CARE PATIENTS WITH PERITONITIS, MULTIPLE INJURY, AND NECROTIZING PANCREATITIS [J].
BUCHLER, M ;
DELLER, A ;
MALFERTHEINER, P ;
KLEINE, HO ;
WIEDECK, H ;
UHL, W ;
SAMTNER, M ;
FRIESS, H ;
NEVALAINEN, T ;
BEGER, HG .
KLINISCHE WOCHENSCHRIFT, 1989, 67 (03) :217-221
[8]  
BUCHLER M, 1989, GASTROENTEROLOGY, V97, P1521
[9]  
Castagnelo B, 2000, ANN ONCOL, V11, P2
[10]   A STUDY OF PHOSPHOLIPASE A2-INDUCED EDEMA IN RAT PAW [J].
CIRINO, G ;
PEERS, SH ;
WALLACE, JL ;
FLOWER, RJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1989, 166 (03) :505-510