Rosiglitazone-induced protection against myelotoxicity produced by 5-fluorouracil

被引:11
作者
Benkö, I
Djazayeri, K
Abrahám, C
Zsuga, J
Szilvássy, Z
机构
[1] Univ Debrecen, Med & Hlth Sci Ctr, Dept Pharmacol & Pharmacotherapy, H-4012 Debrecen, Hungary
[2] N Gene Res Labs Inc, H-1106 Budapest, Hungary
关键词
thiazolidinedione; CFU-GM; bone marrow toxicity; insulin sensitizer;
D O I
10.1016/j.ejphar.2003.08.021
中图分类号
R9 [药学];
学科分类号
1007 ;
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. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:179 / 182
页数:4
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