Many different cell types, coordinated by proinflammatory mediators, t
ake part in the acute inflammatory reaction, but there is a lack of ev
idence regarding the role of erythroid cells in such conditions. In th
is study, changes in bone marrow, splenic, and peripheral blood erythr
oid cells and in erythropoietin (Epo) blood levels were investigated u
p to 72 hours after polyvinylpyrrolidone (PVP)-induced sterile inflamm
ation in male Wistar rats (two intraperitoneal injections of 15 mL 3.5
% PVP at 18-hour intervals). Transient changes within progenitor eryth
roid cells were observed in the bone marrow. Significant increases in
the number of splenic immature erythroid progenitors (BFU-E) 6 hours a
nd mature erythroid progenitors (CFU-E), erythroblasts, and orthochrom
atic erythroblasts 48 and 72 hours after the induction of inflammation
pointed to stimulated splenic erythropoiesis. This was confirmed by s
emiquantitative assessment of splenic smears, which demonstrated expan
sion of erythroid cells at hours 48 and 72. The changes observed in th
e bone marrow and spleen indicated that during acute inflammation eryt
hropoiesis was stimulated and that the spleens of PVP-treated rats wer
e favorable to erythroid development. The significant increase in the
percentage of peripheral blood reticulocytes 48 and 72 hours after PVP
-induced inflammation provided evidence that effective erythropoiesis
occurred. In spite of the stimulated erythropoiesis, serum levels of E
po remained unchanged, implying that other non-Epo regulatory molecule
s may be responsible for erythroid cellular changes.