TY - JOUR
T1 - The distribution of endogenous epidermal growth factor after small bowel resection suggests increased intestinal utilization during adaptation
AU - Shin, Cathy E.
AU - Falcone, Richard A.
AU - Duane, Katherine R.
AU - Erwin, Christopher R.
AU - Warner, Brad W.
N1 - Funding Information:
From the Division of Pediatric Surges Children k Hospital Medical Center: Department of SurgeT, Liniversiv of Cincinnati College of Medicine, Cincinnati, OH. Presented at the 29th Annual Meeting of the American Pediatric Surgical Association, Hilton Head, South Carolina, May 10-13. 1998. Supported by a Trustees Grantfrom the Children’s Hospital Research Foundation; Children’s Hospital Medical Center; Cincinnati, OH and National Institutes of Health RO-1 DK 53234.01 (Dr Warner-grant recipient). Address reprint requests to Brad W Warner; MD. Division of Pediatric Surges, Childrenk Hospital Medical Centec 3333 Burner Ave, Cincinnati OH 45229.3039. Copyright 0 1999 b.v WB. Saunders Cornpan?: 0022.3468/99/3401-0005$03.00/O 1183 t 119 nmol sham, PC .05) and decreased urinary (417 ? 58 nmol SBR v 940 2 143 nmol sham; P < .05) EGF levels. EGF-R activation increased 2.5-fold after SBR.
PY - 1999/1
Y1 - 1999/1
N2 - Background/Purpose: Although exogenous epidermal growth factor (EGF) amplifies adaptation after massive small bowel resection (SBR), the role for endogenous EGF is unclear. The authors sought to determine whether SBR was associated with changes in the levels of EGF in the serum, saliva, or urine and EGF receptor (EGF-R) signaling in the ileum. Methods: Male ICR mice underwent 50% proximal SBR or sham surgery bowel transection/reanastomosis). After 3 days, levels of EGF were measured by enzyme-linked immunosorbent assay (ELISA) in the serum, saliva, and urine. EGF-R activation was measured in isolated ileal enterocytes by probing an EGF-R immunoprecipitate with an antibody to phosphotyrosine. Results: When compared with sham, SBR resulted in no change in serum, increased salivary (2209 ± 266 nmol SBR v 1183 ± 119 nmol sham, P<.05) and decreased urinary (417 ± 58 nmol SBR v 940 ± 143 nmol sham; P< .05) EGF levels. EGF-R activation increased 2.5-fold after SBR. Conclusions: increased salivary and reduced urinary EGF linked with enhanced EGF-R activation suggests increased ileal utilization of EGF during adaptation. This observation, along with the known beneficial effects of exogenous EGF, infers a crucial role for endogenous EGF in the pathogenesis of intestinal adaptation after SBR.
AB - Background/Purpose: Although exogenous epidermal growth factor (EGF) amplifies adaptation after massive small bowel resection (SBR), the role for endogenous EGF is unclear. The authors sought to determine whether SBR was associated with changes in the levels of EGF in the serum, saliva, or urine and EGF receptor (EGF-R) signaling in the ileum. Methods: Male ICR mice underwent 50% proximal SBR or sham surgery bowel transection/reanastomosis). After 3 days, levels of EGF were measured by enzyme-linked immunosorbent assay (ELISA) in the serum, saliva, and urine. EGF-R activation was measured in isolated ileal enterocytes by probing an EGF-R immunoprecipitate with an antibody to phosphotyrosine. Results: When compared with sham, SBR resulted in no change in serum, increased salivary (2209 ± 266 nmol SBR v 1183 ± 119 nmol sham, P<.05) and decreased urinary (417 ± 58 nmol SBR v 940 ± 143 nmol sham; P< .05) EGF levels. EGF-R activation increased 2.5-fold after SBR. Conclusions: increased salivary and reduced urinary EGF linked with enhanced EGF-R activation suggests increased ileal utilization of EGF during adaptation. This observation, along with the known beneficial effects of exogenous EGF, infers a crucial role for endogenous EGF in the pathogenesis of intestinal adaptation after SBR.
KW - Enterectomy
KW - Epidermal growth factor receptor
KW - Intestinal adaptation
KW - Mice
KW - Phosphotyrosine
KW - Receptor activation
KW - Short bowel syndrome
UR - http://www.scopus.com/inward/record.url?scp=0032958796&partnerID=8YFLogxK
U2 - 10.1016/S0022-3468(99)90222-1
DO - 10.1016/S0022-3468(99)90222-1
M3 - Article
C2 - 10022137
AN - SCOPUS:0032958796
SN - 0022-3468
VL - 34
SP - 22
EP - 26
JO - Journal of Pediatric Surgery
JF - Journal of Pediatric Surgery
IS - 1
ER -