Comparison of interleukin-11 and epidermal growth factor on residual small intestine after massive small bowel resection

被引:38
作者
Fiore, NF
Ledniczky, G
Liu, Q
Orazi, A
Du, XX
Williams, DA
Grosfeld, JL
机构
[1] Indiana Univ, Sch Med, Dept Surg, Pediat Surg Sect, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Pathol & Lab Med, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Howard Hughes Med Inst, Indianapolis, IN 46202 USA
关键词
interleukin-11; cytokines; epidermal growth factor; short bowel syndrome; intestinal adaptation;
D O I
10.1016/S0022-3468(98)90354-2
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background/Purpose: Interleukin 11 (IL-11) is a multifunctional cytokine derived from bone marrow, which has a trophic effect on small bowel epithelium. This study compares the effects of IL-11 with epidermal growth factor (EGF), a growth factor known to enhance small bowel adaptation. Methods: Forty Sprague-Dawley rats (90 to 100 g) underwent an 85% mid-small bowel resection with primary anastomosis on day 0. Rats were divided into four treatment groups: controls (group I) received bovine serum albumin (BSA), group II received IL-11, 125 mu g/kg subcutaneously (SC) twice daily, group III received EGF, 0.10 mu g/g SC bid, and group IV received EGF and IL-11 in the above doses. Half of the animals (five per group) were killed on day 4 of therapy, and the rest were killed on day 8. Animals were evaluated for weight, mucosal length, and bowel wall muscle thickness on days 4 and 8, and expression of proliferating cell nuclear antigen (PCNA) in intestinal crypt and smooth muscle cells on day 8. Results: There were two deaths; both were 8-day controls. Body weight was similar at day 4 and day 8. Mucosal thickness in groups II (IL-11) and group IV (IL-11 and EGF) was significantly increased at day 4 and 8 when compared with controls (group 1) and EGF (group III, P<.001). Muscle thickness was significantly increased in the EGF and combined group IV compared with the BSA controls and IL-11 groups (P <.001). Thirty-two percent of the mucosal crypt cells in Group I stained positive for PCNA, whereas 51%, 53%, and 60% stained positive in groups II (IL-11), III (EGF), and IV (IL-11 and EGF), respectively. In groups I and II, 2% and 1.7% of the myocytes stained positive for PCNA, whereas 11.2% and 5.2% of the myocytes in group III and IV stained positive. Conclusions: These data suggest that IL-11 has a trophic effect on small intestinal enterocytes, causing cell proliferation and increased mucosal thickness. EGF has a more generalized effect on intestine causing proliferation of both enterocytes and myocytes, IL-11, with or without EGF, may be a useful adjunct in instances of short bowel syndrome. Copyright (C) 1998 by W.B. Saunders Company.
引用
收藏
页码:24 / 29
页数:6
相关论文
共 33 条
[11]   MITOGENS FOR ADULT-RAT AORTIC VASCULAR SMOOTH-MUSCLE CELLS IN SERUM-FREE PRIMARY CULTURE [J].
GRAINGER, DJ ;
WITCHELL, CM ;
WEISSBERG, PL ;
METCALFE, JC .
CARDIOVASCULAR RESEARCH, 1994, 28 (08) :1238-1242
[12]   TYROSINE KINASE PATHWAYS AND THE REGULATION OF SMOOTH-MUSCLE CONTRACTILITY [J].
HOLLENBERG, MD .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (04) :108-114
[13]   SHORT-TERM EFFECT OF EPIDERMAL GROWTH FACTOR (EGF) ON SODIUM AND GLUCOSE COTRANSPORT OF ISOLATED JEJUNAL EPITHELIAL-CELLS [J].
HORVATH, K ;
HILL, ID ;
DEVARAJAN, P ;
MEHTA, D ;
THOMAS, SC ;
LU, RB ;
LEBENTHAL, E .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1994, 1222 (02) :215-222
[14]   IGF-I AND THE TRUNCATED ANALOG DES-(1-3)IGF-I ENHANCE GROWTH IN RATS AFTER GUT RESECTION [J].
LEMMEY, AB ;
MARTIN, AA ;
READ, LC ;
TOMAS, FM ;
OWENS, PC ;
BALLARD, FJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (02) :E213-E219
[15]   Trophic effects of interleukin-11 in rats with experimental short bowel syndrome [J].
Liu, Q ;
Du, XX ;
Schindel, DT ;
Yang, ZX ;
Rescorla, FJ ;
Williams, DA ;
Grosfeld, JL .
JOURNAL OF PEDIATRIC SURGERY, 1996, 31 (08) :1047-1050
[16]   BIOLOGICAL EFFECTS OF EPIDERMAL GROWTH-FACTOR, WITH EMPHASIS ON THE GASTROINTESTINAL-TRACT AND LIVER - AN UPDATE [J].
MARTI, U ;
BURWEN, SJ ;
JONES, AL .
HEPATOLOGY, 1989, 9 (01) :126-138
[17]  
OPELTAMADSEN K, 1994, GASTROENTEROLOGY, V107, P87
[18]  
Orazi A, 1996, LAB INVEST, V75, P33
[19]  
POTTEN CS, 1989, CHEM INDUCED CELL PR, P155
[20]  
READ LC, 1986, ENDOCRINOL EXP, V20, P199