EPIDERMAL GROWTH-FACTOR PROTECTS GASTRIC-MUCOSA AGAINST ISCHEMIA-REPERFUSION INJURY

被引:12
作者
ISHIKAWA, T
TARNAWSKI, A
SARFEH, IJ
STACHURA, J
机构
[1] VET ADM MED CTR,GASTROENTEROL SECT,5901 E 7TH ST,LONG BEACH,CA 90822
[2] UNIV CALIF IRVINE,IRVINE,CA 92717
关键词
EPIDERMAL GROWTH FACTOR; ISCHEMIA REPERFUSION; GASTRIC MUCOSAL DAMAGE; MICROVASCULAR PERMEABILITY; MICROVESSELS; ENDOTHELIAL CELLS; MUCOSAL PROTECTION;
D O I
10.1097/00004836-199312001-00019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Epidermal growth factor (EGF) protects gastric mucosa against many injurious factors, but no study has examined whether EGF may protect against ischemia-reperfusion (I-R)-induced gastric mucosal injury. We assessed the effect of EGF pretreatment on the extent of ischemia-reperfusion-induced gastric mucosal damage in rats. Assessment of injury and protection included: the extent of macroscopic necrosis; qualitative and quantitative histology with measurement of deep mucosal necrosis; microvascular permeability after injection of fluorescein-conjugated albumin; and transmission electron microscopy. After I-R, saline-pretreated rats (placebo group) had macroscopic necrosis involving 40 +/- 6% of total gastric mucosal area. Histology revealed exfoliation of the surface epithelial cells, mucosal hemorrhages, microvascular injury, and extensive deep mucosal necrosis involving 7 +/- 5% of mucosal strips. Microvascular permeability assessed by fluorescein-conjugated albumin was significantly increased to 327 +/- 29% of that in normal rats (without ischemia-reperfusion). Transmission electron microscopy showed severe microvascular injury. EGF pretreatment significantly reduced gross mucosal necrosis to 17 +/- 6% and deep histologic mucosal necrosis to 2 +/- 1% (both p < 0.01 versus saline pretreated). Integrity of the mucosal microvessels was preserved and microvascular permeability was close to normal. This study demonstrates that EGF significantly reduces ischemia-reperfusion injury to the rat gastric mucosa and that this effect of EGF may be mediated by its protection of the mucosal microvessels.
引用
收藏
页码:S104 / S110
页数:7
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