Female rats were loaded with lead acetate (5 mg Pb/kg) during 2 weeks (10 t
imes) intraperitoneally. Four-day chelation treatment started 1 week later
with CaNa2 ethylenediaminetetraacerate (EDTA, 0.3 mmol/kg i.p. at 4:00 p.m.
), and meso- or raceinic-2,3-dimercaptosuccinic acid (meso- or rac-DMSA, 0.
5 mmol/kg p.o. at 10:00 a.m.). One group was administered EDTA as monothera
py, and two groups received combined treatment with EDTA plus either mcso-D
MSA or rac-DMSA. Lead was determined in femur, kidneys, and brain. Urinary
eliminations of lead, iron, zinc, and copper were also evaluated. With EDTA
monotherapy, lead was reduced in kidneys. Combined treatment with EDTA plu
s meso-DMSA reduced lead in kidneys and brain, and EDTA plus rac-DMSA treat
ment reduced lead in femur, kidneys, and brain. Urine lead elimination was
increased by EDTA monotherapy 10 times, and by both combined treatments 14-
15 times. Urine zinc excretion was increased by both EDTA monotherapy and i
n combined treatment with meso-DMSA 3-4, times, and in combined treatment w
ith mc-DMSA 5-6 times. Both combined treatments increased copper urinary ex
cretion 3-4 times. Best results in reducing tissue lead were obtained when
EDTA therapy was combined with mc-DMSA treatment. Since this combination al
so caused highest urinary trace element elimination, more data are needed b
efore recommending rac-DMSA for use in combined treatment of lead poisoning
. J. Trace Elem. Exp. Med. 13:277-284, 2000. (C) 2000 Wiley-Liss, Inc.