INVIVO PROFILES OF EICOSANOIDS IN ULCERATIVE-COLITIS, CROHNS COLITIS, AND CLOSTRIDIUM-DIFFICILE COLITIS

被引:181
作者
LAURITSEN, K
LAURSEN, LS
BUKHAVE, K
RASKMADSEN, J
机构
[1] UNIV COPENHAGEN, BISPEBJERG HOSP, DEPT MED B, GASTROENTEROL SECT, DK-2400 COPENHAGEN NV, DENMARK
[2] ODENSE UNIV HOSP, DEPT MED GASTROENTEROL, DK-5000 ODENSE, DENMARK
[3] UNIV COPENHAGEN, HERLEV HOSP, DEPT MED C, GASTROENTEROL SECT, DK-2730 HERLEV, DENMARK
关键词
D O I
10.1016/0016-5085(88)90284-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
To compare the local release of arachidonic acid metabolites in inflammatory diarrheal disease, in vivo equilibrium dialysis of the rectum was done in consecutive untreated patients with ulcerative colitis (n = 20), Crohn''s colitis (n = 10, and Clostridium difficile colitis (n = 7). All patients had endoscopically proven rectal inflammation. Eicosanoid profiles were determined in rectal dialysates by radioimmunoassay after preliminary purification. Concentrations of prostaglandin E2, prostaglandin F2.alpha., and thromboxane B2, but not 6-ketoprostaglandin F1.alpha., were raised in all groups and compared with healthy controls. The highest levels within each group were obtained in patients with widespread epithelial damage, as judged by endoscopy. In patients with ulcerative colitis, an extreme rise in prostaglandin E2 and thromboxane B2 were observed. Similarly, concentrations of leukotriene B4 were substantially increased in ulcerative colitis, but in Crohn''s colitis and Clostridium difficile colitis only those patients with rectal ulcerations showed elevations. These findings probably reflect more severe tissue damage in ulcerative colitis, but differences between disease groups in cell-to-cell interaction may also contribute. The data suggest, therefore, that therapeutic inhibition of lipoxygenase pathways may prove more effective in ulcerative colitis than in Crohn''s disease.
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页码:11 / 17
页数:7
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