Gastric and small bowel ileus after severe burn in rats: The effect of cyclooxygenase-2 inhibitors

被引:18
作者
Oliveira, Hermes M. [3 ,5 ]
Sallam, Hanaa S. [3 ,4 ]
Espana-Tenorio, Jonathan [2 ]
Chinkes, David [2 ]
Chung, Dai H. [2 ]
Chen, Jiande D. Z. [3 ]
Herndon, David N. [1 ,2 ]
机构
[1] Shriners Hosp Children, Med Staff, Galveston, TX 77550 USA
[2] Univ Texas Med Branch, Dept Surg, Galveston, TX USA
[3] Univ Texas Med Branch, Dept Internal Med, Div Gastroenterol, Galveston, TX USA
[4] Suez Canal Univ, Dept Physiol, Fac Med, Ismailia, Egypt
[5] Univ Fed Minas Gerais, Belo Horizonte, MG, Brazil
关键词
Burn; COX-2; inhibitors; Gastric emptying; Small bowel ileus; TRAUMATIC BRAIN-INJURY; POSTOPERATIVE ILEUS; THERMAL-INJURY; COX-2; EXPRESSION; INFLAMMATION; KETOROLAC; MOTILITY; DISEASE; SURGERY;
D O I
10.1016/j.burns.2009.02.022
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Gastrointestinal (GI) ileus is a common complication after severe burns. Selective cyclooxygenase-2 inhibitors (COX-2i) improved post-operative ileus, but its effect on burn-induced GI dysmotility is unknown. Our aim was to test whether a COX-2i improves gastric emptying (GE) and small bowel transit (SBT) after burn. Experiment on GE: rats were anesthetized and randomized into sham/scald burn, treated/untreated with COX-2i. Six hours after burn, rats received a phenol red meal and were sacrificed 30 min later. Gastric emptying was determined based on the percentage of phenol red recovered in harvested stomachs. Experiment on SBT: rats received a duodenostomy and were scald/sham burned 5 days later. Six hours after burn, rats received a phenol red meal through the duodenostomy catheter and were sacrificed 100 min later. Geometric center (GC) was calculated for SBT. GE was decreased significantly in burned vs. sham animals (p < 0.001). SBT was significantly impaired in burned vs. sham animals (p < 0.001). The COX-2i improved GE in the burn rats but not GE in the control rats or SBT in the burn rats. COX-2i improves bum-induced delayed GE, suggesting the mediation of the latter via the prostaglandin pathway. (C) 2009 Published by Elsevier Ltd and ISBI.
引用
收藏
页码:1180 / 1184
页数:5
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