促红细胞生成素与U-74389G降血糖作用的比较

C. Tsompos, C. Panoulis, K. Toutouzas, A. Triantafyllou, C. Zografos, A. Papalois, K. Tsarea, M. Karamperi
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引用次数: 2

摘要

目的:计算促红细胞生成素(Epo)和抗氧化药物U-74389G的降糖能力。该计算基于2项初步研究的结果,每一项研究都是在诱导缺氧再氧化动物实验中评估各自药物使用后对低血糖的影响。材料与方法:测定葡萄糖(Gl)水平的2个主要实验终点为第60次再氧化min (A、C、E组)和第120次再氧化min (B、D、F组),其中A、B组为未用药处理,C、D组为给药后处理;而E组和F组经U-74389G处理后。结果:第一次初步研究Epo的降糖作用为0.84%+1.12% (p值=0.4430)。第二次初步研究U-74389G降糖效果为3.94%+1.06% (p值=0.0005)。这两项研究是共同评估的,因为它们来自相同的实验环境。联合评价结果为U-74389G的降糖效力是Epo的4.660603倍(p值=0.0000)。结论:U-74389G抗氧化能力增强急性降糖作用,其急性降糖作用是Epo的4.660603倍(p值=0.0000)。
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Comparison of the Hypoglucemic Effects of Erythropoietin and U-74389G on Glucose Levels
Aim: This study calculated the hypoglucemic capacities of 2 drugs: the erythropoietin (Epo) and the antioxidant drug U-74389G. The calculation was based on the results of 2 preliminary studies, each one of which estimated the hypoglucemic influence, after the respective drug usage in an induced hypoxia reoxygenation animal experiment. Materials and Methods: The 2 main experimental endpoints at which the glucose (Gl) levels were evaluated was the 60th reoxygenation min (for the groups A, C and E) and the 120th reoxygenation min (for the groups B, D and F). Specially, the groups A and B were processed without drugs, groups C and D after Epo administration; whereas groups E and F after U-74389G administration. Results: The first preliminary study of Epo presented a non significant hypoglucemic effect by 0.84%+1.12% (p-value=0.4430). The second preliminary study of U-74389G presented a significant hypoglucemic effect by 3.94%+1.06% (p-value=0.0005). 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 4.660603-fold more hypoglucemic potency than Epo (p-value=0.0000). Conclusions: The anti-oxidant capacities of U-74389G enhance the acute hypoglucemic properties presenting 4.660603-fold more intentive hypoglucemia than Epo (p-value=0.0000).
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