Rosiglitazone-induced protection against myelotoxicity produced by 5-fluorouracil

Eur J Pharmacol. 2003 Sep 12;477(2):179-82. doi: 10.1016/j.ejphar.2003.08.021.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Antimetabolites, Antineoplastic / adverse effects*
  • Bone Marrow / drug effects*
  • Bone Marrow / metabolism
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Colony-Forming Units Assay
  • Female
  • Fluorouracil / adverse effects*
  • Granulocytes / drug effects
  • Hematopoietic Stem Cells / drug effects
  • Hypoglycemic Agents / pharmacology
  • Injections, Intraperitoneal
  • Insulin Resistance
  • Macrophages / drug effects
  • Mice
  • Neutropenia / chemically induced
  • Neutropenia / prevention & control
  • Protective Agents / pharmacology*
  • Rosiglitazone
  • Thiazolidinediones / pharmacology*

Substances

  • Antimetabolites, Antineoplastic
  • Hypoglycemic Agents
  • Protective Agents
  • Thiazolidinediones
  • Rosiglitazone
  • Fluorouracil