Chronic ethanol administration decreases rat pancreatic GP2 content

被引:12
作者
Apte, MV
Norton, ID
Haber, PS
Korsten, MA
McCaughan, GW
Pirola, RC
Wilson, JS
机构
[1] PRINCE WALES HOSP,DEPT GASTROENTEROL,GASTROINTESTINAL UNIT,RANDWICK,NSW 2031,AUSTRALIA
[2] UNIV NEW S WALES,SYDNEY,NSW,AUSTRALIA
[3] MT SINAI SCH MED,ALCOHOL RES CTR,NEW YORK,NY
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 1997年 / 1336卷 / 01期
基金
英国医学研究理事会;
关键词
GP2; zymogen granule; ethanol; alcoholic pancreatitis;
D O I
10.1016/S0304-4165(97)00015-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Postulated mechanisms of alcoholic pancreatitis include (i) zymogen granule fragility facilitating intracellular activation of digestive enzymes and (ii) ductular obstruction by protein plugs. GP2, a pancreatic glycoprotein, stabilizes zymogen granule membranes and is an important constituent of pancreatic protein plugs. Therefore, this study examined the pancreatic content and messenger RNA levels of GP2 after chronic ethanol administration. Rats were fed liquid diets with or without ethanol, for four weeks. GP2 levels in pancreatic homogenates, crude zymogen granules and zymogen granule membrane fractions were assessed by immunoblotting. Messenger RNA levels for GP2 were measured by Northern and dot blotting of pancreatic RNA. Pancreatic GP2 levels were lower in ethanol-fed rats than in controls (GP2 levels expressed as % of control: 38.75 +/- 5.8, p < 0.001 in homogenate; 31.28 +/- 3.5, p < 0.0005 in crude zymogen granules and 22.89 +/- 5.4, p < 0.0005 in zymogen granule membranes). Messenger RNA levels for GP2 were unchanged after ethanol feeding. Chronic ethanol consumption decreases GP2 content of pancreatic homogenate and zymogen granules. This decrease could (i) result from an increased release into pancreatic juice thereby favouring protein plug formation and (ii) impair zymogen granule stability. Both these mechanisms could potentiate pancreatic damage. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:89 / 98
页数:10
相关论文
共 28 条
[1]   HIGH-RESOLUTION ANALYSIS OF THE HUMAN HLA-DR POLYMORPHISM BY HYBRIDIZATION WITH SEQUENCE-SPECIFIC OLIGONUCLEOTIDE PROBES [J].
ANGELINI, G ;
DEPREVAL, C ;
GORSKI, J ;
MACH, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (12) :4489-4493
[2]  
APTE MV, 1995, J LAB CLIN MED, V125, P634
[3]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[4]  
DIMAGNO EP, 1993, PANCREAS BIOL PATHOB, P668
[5]  
DITTIE A, 1992, EUR J CELL BIOL, V58, P243
[6]  
FELDMAN DS, 1987, STATVIEW 2
[7]   NONPARALLEL SECRETION OF GP-2 FROM EXOCRINE PANCREAS IMPLIES LUMINAL COUPLING BETWEEN ACINAR AND DUCT CELLS [J].
FREEDMAN, SD ;
SAKAMOTO, K ;
SCHEELE, GA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (01) :G40-G51
[8]  
FREEDMAN SD, 1993, EUR J CELL BIOL, V61, P229
[9]   GP2, THE HOMOLOG TO THE RENAL CAST PROTEIN UROMODULIN, IS A MAJOR COMPONENT OF INTRADUCTAL PLUGS IN CHRONIC-PANCREATITIS [J].
FREEDMAN, SD ;
SAKAMOTO, K ;
VENU, RP .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :83-90
[10]  
GUY O, 1983, GASTROENTEROLOGY, V84, P102