PROTECTIVE EFFECT OF EPIDERMAL GROWTH-FACTOR IN AN EXPERIMENTAL-MODEL OF COLITIS IN RATS

被引:135
作者
PROCACCINO, F [1 ]
REINSHAGEN, M [1 ]
HOFFMANN, P [1 ]
ZEEH, JM [1 ]
LAKSHMANAN, J [1 ]
MCROBERTS, JA [1 ]
PATEL, A [1 ]
FRENCH, S [1 ]
EYSSELEIN, VE [1 ]
机构
[1] UNIV CALIF LOS ANGELES,HARBOR MED CTR,CTR INFLAMMATORY BOWEL DIS,TORRANCE,CA 90509
关键词
D O I
10.1016/0016-5085(94)90055-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The role of epidermal growth factor (EGF) in the maintenance of mucosal integrity in the lower gastrointestinal tract is unknown. The aim of this study was to determine the effect of EGF in experimental colitis. Methods: Colitis was induced with 2,4,6-trinitrobenzenesulfonic acid/ethanol enemas. Rats were pretreated with intraperitoneal administration of recombinant human EGF (600 μg/kg) or vehicle 1 hour before induction of colitis and daily thereafter until killed at 8 hours, 48 hours, and 1 week. A separate group received an identical dosage and administration of EGF or vehicle for 1 week with treatment initiated 24 hours after the induction of colitic. Colonic tissue was evaluated macroscopically, histologically, and for myeloperoxidase activity. Results: Pretreatment with EGF reduced microscopic erosions at 8 and 48 hours by 74% and 54%, respectively (P < 0.05). At 1 week, microscopic ulcerations and myeloperoxidase activity were reduced by 65% in the EGF-pretreated group (P < 0.05). No significant difference in macroscopic injury, histological damage, or myeloperoxidase activity was noted when EGF treatment was initiated after the induction of colitis. Conclusions: Systemic EGF administration reduces mucosal damage and inflammation in a trinitrobenzenesulfonic acid/ethanol model of colitis in rats through a mechanism involving mucosal protection. © 1994.
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页码:12 / 17
页数:6
相关论文
共 27 条
[1]   EXPRESSION AND SECRETION OF TYPE-BETA TRANSFORMING GROWTH-FACTOR BY ACTIVATED HUMAN MACROPHAGES [J].
ASSOIAN, RK ;
FLEURDELYS, BE ;
STEVENSON, HC ;
MILLER, PJ ;
MADTES, DK ;
RAINES, EW ;
ROSS, R ;
SPORN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6020-6024
[2]  
BASS P, 1993, J PHARMACOL EXP THER, V264, P984
[3]  
BENEZRA J, 1990, AM J PATHOL, V137, P755
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   ANTIBODIES TO THE EPIDERMAL GROWTH-FACTOR RECEPTOR BLOCK THE BIOLOGICAL-ACTIVITIES OF SARCOMA GROWTH-FACTOR [J].
CARPENTER, G ;
STOSCHECK, CM ;
PRESTON, YA ;
DELARCO, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (18) :5627-5630
[6]   EPIDERMAL GROWTH-FACTOR STIMULATES PROSTAGLANDIN-E RELEASE FROM ISOLATED PERFUSED RAT STOMACH [J].
CHIBA, T ;
HIRATA, Y ;
TAMINATO, T ;
KADOWAKI, S ;
MATSUKURA, S ;
FUJITA, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 105 (01) :370-374
[7]   TRANSFORMING GROWTH FACTOR-ALPHA - STRUCTURE AND BIOLOGICAL-ACTIVITIES [J].
DERYNCK, R .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1986, 32 (04) :293-304
[8]   PROLIFERATIVE EFFECTS OF UROGASTRONE-EGF ON THE INTESTINAL EPITHELIUM [J].
GOODLAD, RA ;
WILSON, TJG ;
LENTON, W ;
GREGORY, H ;
MCCULLAGH, KG ;
WRIGHT, NA .
GUT, 1987, 28 :37-43
[9]   INTERACTION BETWEEN OXYGEN RADICALS AND GASTRIC MUCIN [J].
GRISHAM, MB ;
VONRITTER, C ;
SMITH, BF ;
LAMONT, JT ;
GRANGER, DN .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (01) :G93-G96
[10]   STIMULATION OF RAT OXYNTIC GLAND MUCOSAL GROWTH BY EPIDERMAL GROWTH-FACTOR [J].
JOHNSON, LR ;
GUTHRIE, PD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1980, 238 (01) :G45-G49