THE EFFECT OF ILOPROST AND NDGA IN ISCHEMIA REPERFUSION INJURY IN RAT-LIVER

被引:25
作者
OKBOY, N
YEGEN, C
AKTAN, AO
DOSLUOGLU, HH
SAV, A
YALIN, R
ERCAN, S
机构
[1] MARMARA UNIV, SCH MED, DEPT GEN SURG, GEN CERRAHI BOLUMU, ISTANBUL 81190, TURKEY
[2] MARMARA UNIV, SCH MED, DEPT PATHOL, ISTANBUL 81190, TURKEY
[3] GAZI UNIV, SCH MED, DEPT PHARMACOL, GAZI, TURKEY
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 1992年 / 47卷 / 04期
关键词
D O I
10.1016/0952-3278(92)90200-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, the effects of iloprost (ZK 36374) and NDGA on warm ischemia and reperfusion injury in rat liver were investigated. Rats were given isotonic saline (control group), iloprost 25 mug/kg i.v. (group II) just before warm ischemia or NDGA 10 mug/kg i.v. (group III) 5 min before reperfusion or the same drug were given together (group IV). Serum SGOT, SGPT, and LDH values and tissue malonedialdehyde (MDA), gluthathione (GSH), prostaglandin (PGE2, and leukotriene (LT)C4 levels were determined after ischemia-reperfusion injury. Histopathologic examination of the liver was carried out under the light microscope. The serum SGOT, SGPT and LDH levels improved significantly in groups II, III, and IV when compared with the control group (p < 0.05). There was a significant decrease (p < 0.05) in tissue MDA levels and significant increase (p < 0.05) in tissue GSH levels in group I, when compared with group IV and the control groups. The values did not differ significantly in group IV when compared to controls. The LTC4/PGE, ratio was low and histologic findings were worse in group III. In conclusion, iloprost was found to,be beneficial in preventing the ischemia-reperfusion injury in the rat livers. NDGA, either by direct toxic effector by Shifting the arachidonic acid metabolism to the cyclooxygenase route, was not found to be as effective. Iloprost and NDGA did not exert a synergistic effect.
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收藏
页码:291 / 295
页数:5
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