Comparison of CFU-GM response to piperazinedione versus cyclophosphamide in normal mice.
OKunewick Jp, Buffo Mj, Kociban Dl
Abstract
OKunewick Jp, Buffo Mj, Kociban Dl
Abstract
The effects of cyclophosphamide and piperazinedione on marrow granulocyte-macrophage precursor (CFU-GM) cells were compared in a mouse model. Endogenous colony-forming unit ( ECFU -S) assays after drug exposure were utilized in selecting doses of the two drugs with approximately equal hematopoietic stem cell ablative potential. The selected doses were 20 mg/kg of piperazinedione and 325 mg/kg of cyclophosphamide. Injection of these doses resulted in an initial (3-h) marrow CFU-GM depression of 90% in the cyclophosphamide-treated mice and 98% in the piperazinedione-treated mice. Recovery began within 6-24 h and proceeded in a similar fashion for both groups of animals, peaking at levels near normal control values for CFU-GM at three days after exposure. Both groups showed a subsequent decline to a second nadir at nine days followed by a second recovery toward normal levels. The data suggest that the two drugs affect the CFU-GM in a similar fashion.
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The effects of cyclophosphamide and piperazinedione on marrow granulocyte-macrophage precursor (CFU-GM) cells were compared in a mouse model. Endogenous colony-forming unit ( ECFU -S) assays after drug exposure were utilized in selecting doses of the two drugs with approximately equal hematopoietic stem cell ablative potential. The selected doses were 20 mg/kg of piperazinedione and 325 mg/kg of cyclophosphamide. Injection of these doses resulted in an initial (3-h) marrow CFU-GM depression of 90% in the cyclophosphamide-treated mice and 98% in the piperazinedione-treated mice. Recovery began within 6-24 h and proceeded in a similar fashion for both groups of animals, peaking at levels near normal control values for CFU-GM at three days after exposure. Both groups showed a subsequent decline to a second nadir at nine days followed by a second recovery toward normal levels. The data suggest that the two drugs affect the CFU-GM in a similar fashion.
Key concepts: Cyclophosphamide, CFU-GM, Haematopoiesis, Colony-forming unit, Pharmacology, Andrology, Biology, Immunology