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Rosiglitazone-induced protection against myelotoxicity produced by 5-fluorouracil.

机译:罗格列酮诱导的针对5-氟尿嘧啶产生的骨髓毒性的保护作用。

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摘要

Insulin promotes survival of haemopoietic progenitors. We investigated if rosiglitazone, an insulin sensitizer, could confer protection against 5-fluorouracil (5-FU)-induced myelotoxicity in mice. The decrease in bone marrow cellularity, frequency and content of granulocyte-macrophage progenitors (CFU-GM) characterized myelotoxicity in mice, while insulin sensitivity was determined by hyperinsulinaemic euglycaemic glucose clamping. CFU-GM colony numbers increased in groups pre-treated with rosiglitazone (1.5-6 mg/kg, 5 days), compared to that in mice treated with 5-fluorouracil alone. Since rosiglitazone pre-treatment significantly promoted the clonal expansion of CFU-GM when given in the insulin sensitizing dose, we conclude that rosiglitazone had myeloprotective effects possibly by amplifying endogenous insulin action.
机译:胰岛素促进造血祖细胞的存活。我们调查了罗格列酮(一种胰岛素增敏剂)是否可以赋予小鼠抗5-氟尿嘧啶(5-FU)诱导的骨髓毒性的保护作用。骨髓细胞减少,粒细胞巨噬细胞祖细胞(CFU-GM)的频率和含量的降低表征了小鼠的骨髓毒性,而胰岛素敏感性则通过高胰岛素正常血糖固定来确定。与仅用5-氟尿嘧啶治疗的小鼠相比,用罗格列酮预处理的组(1.5-6 mg / kg,5天)的CFU-GM菌落数增加。由于罗格列酮预处理以胰岛素致敏剂量显着促进CFU-GM的克隆扩增,因此我们得出结论,罗格列酮可能通过扩大内源性胰岛素作用而具有骨髓保护作用。

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