Protective effect of iloprost and UK 38 485 against gastric mucosal damage induced by various stimuli

H. Zengil, E. Onuk, Z.S. Ercan, R.K. Türker
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引用次数: 15

Abstract

This study was undertaken to evaluate the efficacy of iloprost and UK 38485 in the prevention of gastric lesions due to restraint-cold stress, ethanol or indomethacin. Prior injection of iloprost to the rats significantly prevented the increase in ulcer index by restraint- cold stress or indomethacin but nonsignificantly reduced the ulcer index induced by ethanol. UK 38 485 at lower doses caused a highly significant decrease in the ulcer index induced by all noxious stimuli used in this study. UK 38 485 also reduced the increased 3H back diffusion due to restraint-cold stress. Higher doses of the compound, however, failed to decrease the mucosal damage due to restraint-cold stress. Combination of iloprost and UK 38 485 produced a further significant decrease in the ulcer index induced by all noxious stimuli and increased 3H back diffusion induced by restraint-cold stress. In relation to these results the importance of PGI2/TXA2 ratio in the production of gastric mucosal lesions is discussed.

伊洛前列素和uk38485对各种刺激引起的胃黏膜损伤的保护作用
本研究旨在评估伊洛前列素和UK 38485在预防限制性冷应激、乙醇或吲哚美辛引起的胃损伤中的疗效。预先注射伊洛前列素可显著抑制冷应激或吲哚美辛引起的溃疡指数升高,但对乙醇引起的溃疡指数无显著降低。较低剂量的UK 38485导致本研究中使用的所有有害刺激引起的溃疡指数显著下降。UK 38485也减少了由于约束冷应力而增加的3H反向扩散。然而,高剂量的化合物未能减少由于抑制冷应激引起的粘膜损伤。伊洛前列素与UK 38485联合使用可进一步显著降低所有有害刺激诱导的溃疡指数,并增加约束-冷应激诱导的3H背扩散。根据这些结果,讨论了PGI2/TXA2比值在胃粘膜病变产生中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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