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幼鼠肠缺血/再灌注损伤肠组织TNF-α和c-fos mRNA的表达 被引量:1

Expression of tumor necrosis factor-α and c-fos mRNA in immature rats' model of gut ischemia/reperfusion injury
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摘要 目的:观察幼鼠肠缺血/再灌注损伤(I/R)不同时点肠组织内肿瘤坏死因子α(TNF-α)、c-fos mRNA表达模式,探讨肠I/R的机制.方法:分离幼鼠肠系膜上动脉,制作动物模型,应用RT-PCR半定量法分析肠组织 TNF-α、c-fos mRNA表达.结果:与假手术组相比,肠组织内TNF-α mRNA缺血30 min显著升高(1.55±0.33 vs 1.07±0.08,P<0.05),再灌注30 min达峰值(3.05 ±0.11),再灌注后60,90 min逐渐下降;c-fos mRNA表达于缺血30 min后升高(0.95±0.13 vs 0.12±0.02,P<0.05),再灌注30 min达峰值 (1.53±0.11),再灌注后60 min迅速下降,再灌注后90 min达基线水平.结论:幼鼠肠I/R损伤介导肠组织内TNF-α和 c-fos mRNA的表达模式.c-fos mRNA表达伴随TNF-α mRNA表达,提示二者间可能存在关系. AIM: To analyze the expression patterns of tumor necrosis factor-or (TNF-α and c-fos mRNA in immature rats after gut ischemia/reperfusion (I/ R) injury. METHODS: The left laparotomy was performed and the superior mesenteric artery (SMA) was occluded by artery clamp to establish the model of gut I/R injury. The expression of TNF-α and c-fos mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). RESULTS: In comparison with sham operation group, an increase in TNF-α mRNA was detected after 30-min ischemia (1.55±0.33 vs 1.07 ±0.08, P〈0.05) and the maximal increase was detected after 30-min reperfusion (3.05±0.11). TNF-α mRNA expression after 60-min reperfusion (2.02±0.10) remained above the control level. The expression of c-fos mRNA in the intestinal tissues was rapidly induced by ischemia, and it increased obviously 30 min after ischemia as compared with that in sham operation group (0.95± 0.13 vs 0.12±0.02, P〈0.05). The expression of c-fos mRNA also reached the peak level 30 min after reperfusion (1.53± 0.11), and it declined markedly 60 min after reperfusion. After 90-min reperfusion, c-fos mRNA expression returned to the normal level. CONCLUSION: Gut I/R induces the mRNA expression of both TNF-α and c-fos, suggesting that there is possibly a correlation between the expression of c-los and TNF-α.
出处 《世界华人消化杂志》 CAS 北大核心 2006年第16期1631-1634,共4页 World Chinese Journal of Digestology
关键词 缺血/再灌注 肿瘤坏死因子 C-FOS基因 Ischemia/reperfusion Tumor necrosisfactor-α Gut c-fos gene
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