Transport of 14C-deferiprone in normal, thalassaemic and sickle red blood cells.

BRITISH JOURNAL OF HAEMATOLOGY(1999)

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摘要
The transport of deferiprone (L1) in normal (N), sickle (S) and thalassaemic (T) red blood cells (RBC) was determined by incubation with C-14-L1 at 37 degrees C. Following incubation with 0.5 mM C-14-L1 for 4 h, the intracellular concentration of L1 in T RBC was 3 times higher than was found extracellularly, In contrast, no concentration gradient across N and S RBC membranes was detected. Efflux studies showed that T RBC released only 17 +/- 2% of C-14-L1 into the extracellular space. We hypothesize that L1 accumulation in T RBC results from their high content of chelatable iron and formation of large. hydrophilic L1-Fe(III) complexes trapped within the cytosol.
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deferiprone,transport,erythrocytes,sickle cell disease,thalassaemia
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