We hypothesized that 4 weeks of recombinant human erythropoietin (RhEPO) treatment would result in a significant increase in haemoglobin concentration ([Hb]) and arterial blood O 2 -carrying capacity and that this would (1) increase peak pulmonary oxygen uptake (V O 2 ) during ramp incremental exercise, and (2) speedV O 2 kinetics during 'severe'-, but not 'moderate'-or 'heavy'-intensity, step exercise. Fifteen subjects (mean ± S.D. age 25 ± 4 years) were randomly assigned to either an experimental group which received a weekly subcutaneous injection of RhEPO (150 IU kg −1 ; n = 8), or a control group (CON) which received a weekly subcutaneous injection of sterile saline (10 ml; n = 7) as a placebo, for four weeks. The subjects and the principal researchers were both blind with respect to the group assignment. Before and after the intervention period, all subjects completed a ramp test for determination of the gas exchange threshold (GET) andV O 2 ,peak , and a number of identical 'step' transitions from 'unloaded' cycling to work rates requiring 80% GET (moderate), 70% of the difference between the GET anḋ V O 2 ,peak (heavy), and 105%V O 2 ,peak (severe) as determined from the initial ramp test. Pulmonary gas exchange was measured breath-by-breath. There were no significant differences between the RhEPO and CON groups for any of the measurements of interest ([Hb],V O 2 ,peak ,V O 2 kinetics) before the intervention. Four weeks of RhEPO treatment resulted in a 7% increase both in [Hb] (from 15.8 ± 1.0 to 16.9 ± 0.7 g dl −1 ; P < 0.01) andV O 2 ,peak (from 47.5 ± 4.2 to 50.8 ± 10.7 ml kg −1 ·min −1 ; P < 0.05), with no significant change in CON. RhEPO had no significant effect onV O 2 kinetics for moderate (Phase II time constant, from 28 ± 8 to 28 ± 7 s), heavy (from 37 ± 12 to 35 ± 11 s), or severe (from 33 ± 15 to 35 ± 15 s) step exercise. Our results indicate that enhancing blood O 2 -carrying capacity and thus the potential for muscle O 2 delivery with RhEPO treatment enhanced the peakV O 2 but did not influenceV O 2 kinetics, suggesting that the latter is principally regulated by intracellular (metabolic) factors, even during exercise where theV O 2 requirement is greater than theV O 2 ,peak , at least in young subjects performing upright cycle exercise.