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Vol. 298, Issue 2, 820-824, August 2001
The Colleges of Pharmacy (S.C., P.V.-P.) and Medicine (R.J.H.,
R.L.S., E.M.M., J.A.W.), Department of Pediatrics, The University of
Iowa, Iowa City, Iowa
The contribution of the bone marrow to in vivo erythropoietin (EPO)
elimination was evaluated by determining EPO pharmacokinetic (PK)
parameters in five adult sheep in a paired manner before and after
chemotherapy-induced marrow ablation. After busulfan-induced bone
marrow ablation, EPO PK demonstrated progressive decreases in plasma
clearance (CL), elimination half-life
[t1/2(
)], and volume of distribution at
steady state (Vss) with concomitant increases in mean residence time (MRT). Eight days after beginning busulfan treatment, there were no further changes in CL,
t1/2(
), MRT, and
Vss. Only 20% of baseline CL remained by
day 8. The volume of distribution (Vc) and
distribution half-life [t1/2(
)], in contrast, remained unchanged from baseline. White blood cell counts and
reticulocytes gradually declined after the start of marrow ablation.
Examination of bone marrow core biopsy samples obtained on day 10 revealed less than 10% of baseline marrow cellularity. No
colony-forming unit erythroid (CFU-E) colonies were found after 6 days
of incubation for bone marrow aspirates drawn at days 8 and 13 following busulfan treatment, whereas pre-busulfan aspirates yielded 29 CFU-E colonies per 105 cells in CFU-E cultures. Treatment
of a sheep with 5-fluorouracil showed changes in PK parameters that
were similar to the results from treatment with busulfan. The present
study indicates that the bone marrow significantly contributes to the
elimination of EPO in vivo.
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