Jd. Lutton et al., Pharmacologic effects of the red blood cell substitutes cross-linked and non-cross-linked hemoglobins on hematopoiesis in rabbits, PHARMACOL, 58(6), 1999, pp. 319-324
The red blood cell substitutes beta-beta crosslinked (DECA-Hb, XLBV-Hb) and
non-cross-linked (HbA) hemoglobins (Hbs), were transfused into rabbits and
their effects on hematopoiesis examined. All rabbits receiving DECA-Hb or
XLBV-Hb tolerated the Hbs well, whereas 50% of the animals transfused with
similar doses of non-cross-linked HbA died. Analysis of peripheral blood an
d bone marrow BFU-E and CFU-GM production revealed that there was no signif
icant variation in the generation of BFU-E and CFU-GM numbers for each cros
s-linked Hb transfusion group, but there were significant reductions in the
HbA group. In animals transfused with cross-linked Hbs, splenic heme oxyge
nase (HO) activity was similar to that of controls; liver HO activity was s
lightly elevated, whereas HO activity was significantly increased in kidney
s. Transfusion with non-cross-linked HbA produced greater inductions of HO
activity in the liver and kidneys. Hepatic delta-aminolevulinic acid syntha
se (ALAS) activity was significantly reduced in HbA-transfused animals, whe
reas transfusion with cross-linked Hbs produced only minor, statistically n
onsignificant, reductions in ALAS activity.