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大鼠缺血再灌注诱导的急性胃损伤不同阶段环氧化酶-1和-2 mRNA的表达水平

Levels of cyclooxygenase-1 and -2 mRNA expression at various stages of acute gastric injury induced by ischemia-reperfusion in rats.

作者信息

Kishimoto Y, Wada K, Nakamoto K, Kawasaki H, Hasegawa J

机构信息

Faculty of Medicine, Tottori University, 86 Nishimachi, Yonago, 683, Japan.

出版信息

Arch Biochem Biophys. 1998 Apr 1;352(1):153-7. doi: 10.1006/abbi.1997.0572.

Abstract

Recently, the state of cyclooxygenase (COX) mRNA expression has been reported in an acetic acid-induced chronic gastric ulcer model of mice. However, the time course of COX expression during the developmental stage and the subsequent repair process of acute gastric injury is not well understood at present. In this study, we quantitatively investigated the time course of the level of COX-2 and -1 mRNA expression from the developmental stage through the healing stage in ischemia-reperfusion (I-R)-induced acute gastric damage. COX-2 mRNA was expressed at low or undetectable levels in the normal gastric tissues of control rats. The COX-2 expression between 6 and 48 h following I-R was higher than that of the control gastric tissues; the histological findings were erosion during 1-36 h and transitional appearance from erosion to ulcer at 48 h. The maximum expression of COX-2 mRNA was recorded at 24 h (approximately 200-fold elevation). The COX-2 message was very low or undetectable at 72 h (ulcer stage) and at 96 and 120 h (healing stage of ulcer) after I-R. The level of COX-1 mRNA remained stable through all stages of acute gastric damage. These results are potentially useful for understanding the role of COX and evaluating the effects of drugs on expression of COX at various stages of acute gastric injury.

摘要

最近,在小鼠乙酸诱导的慢性胃溃疡模型中报道了环氧化酶(COX)mRNA表达的状态。然而,目前对于急性胃损伤发展阶段及随后修复过程中COX表达的时间进程了解尚不清楚。在本研究中,我们定量研究了在缺血再灌注(I-R)诱导的急性胃损伤中,从发展阶段到愈合阶段COX-2和-1 mRNA表达水平的时间进程。在对照大鼠的正常胃组织中,COX-2 mRNA以低水平表达或无法检测到。I-R后6至48小时的COX-2表达高于对照胃组织;组织学结果显示,1至36小时为糜烂,48小时为从糜烂到溃疡的过渡外观。COX-2 mRNA的最大表达在24小时记录(升高约200倍)。I-R后72小时(溃疡期)以及96和120小时(溃疡愈合期),COX-2信息非常低或无法检测到。COX-1 mRNA水平在急性胃损伤的所有阶段保持稳定。这些结果对于理解COX的作用以及评估药物在急性胃损伤各个阶段对COX表达的影响可能是有用的。

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