C. Tsompos, C. Panoulis, K. Toutouzas, A. Triantafyllou, G. Zografos, A. Papalois
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引用次数: 2
摘要
目的在2项初步研究的基础上,比较了促红细胞生成素(Epo)与抗氧化药物U-74389G的造血能力。提供的红细胞压积水平增加的结果在动物模型的缺氧再氧化方案中进行了共同评估。材料与方法测定60只大鼠复氧第60 min (A、C、E组)和第120 min (B、D、F组)的红细胞压积水平。A、B组不给药,C、D组给Epo;E、F组大鼠给予U-74389G。结果第一次初步研究Epo非显著提高红细胞压积0.24%+1.38% (p值=0.8586)。第二次初步研究U-74389G显著提高红细胞压积3.16%+1.33% (p值=0.0196)。这两项研究是共同评估的,因为它们来自相同的实验环境。联合评价的结果是U-74389G的造血效能比Epo高约12.66倍(p值=0.0000)。结论U-74389G具有良好的抗氧化能力,具有良好的急性造血功能;红细胞压积比促红细胞生成素升高约12.66倍(p值=0.0000)。
Comparison of the Acute Hematopoietic Capacities of Erythropoietin and U-74389G Concerning Hematocrit Levels.
AIM
This study compared the hematopoietic capacities of erythropoietin (Epo) and antioxidant drug U-74389G, based on 2 preliminary studies. The provided results on hematocrit levels augmentation were co-evaluated in a hypoxia reoxygenation protocol of an animal model.
MATERIALS AND METHODS
Hematocrit levels were evaluated at the 60th reoxygenation min (for groups A, C and E) and at the 120th reoxygenation min (for groups B, D and F) in 60 rats. Groups A and B received no drugs, rats from groups C and D were administered with Epo; whereas rats from groups E and F were administered with U-74389G.
RESULTS
The first preliminary study of Epo non-significantly increased the hematocrit levels by 0.24%+1.38% (p-value=0.8586). The second preliminary study of U-74389G significantly raised the hematocrit levels by 3.16%+1.33% (p-value=0.0196). These 2 studies were co-evaluated since they came from the same experimental setting. The outcome of the co-evaluation was that U-74389G has approximately 12.66-fold higher hematopoietic potency than Epo (p-value=0.0000).
CONCLUSION
The anti-oxidant capacities of U-74389G provide satisfactory acute hematopoietic properties; presenting approximately 12.66-fold hematocrit level rise than epo (p-value=0.0000).