Placental transfer and fetal distribution of lead in mice after treatment with dithiocarbamates
- PMID: 6329134
- DOI: 10.1007/BF00316582
Placental transfer and fetal distribution of lead in mice after treatment with dithiocarbamates
Abstract
The distribution of i.v. administered lead (203Pb-acetate; 50 nmol/kg b.w.) was studied by means of autoradiography and impulse counting in pregnant C57BL mice (day 18) treated orally with dithiocarbamates. Diethyldithiocarbamate ( DEDTC ), disulfiram or thiram (2 X 1 mmol/kg b.w.) or vehicle ( gelatine ) alone, was given by gavage 2 h before and immediately after the injection of lead. All three dithiocarbamates, especially thiram, changed the distribution pattern of lead. Thiram and DEDTC had the greatest effect at 4 h after lead administration, disulfiram at 24 h. In the mother, most notably the brain concentration increased (70-fold for thiram at 4 h) while that of erythrocytes and skeleton decreased (50- and 4-fold, respectively). The total fetal concentration unexpectedly showed only a moderate increase (approximately 2-fold for thiram), which may be due partly to the low maternal plasma lead concentration. The partition within the fetal tissues was, however, changed by the dithiocarbamates in much the same way as in the mothers, e.g., the fetal brain of thiram treated animals had increased by a factor 15, while skeletal and blood concentrations were lowered compared to controls. In melanin containing structures of the maternal and fetal eyes a dramatic increase in lead concentration resulted from dithiocarbamate treatment (lead ions are known to bind to melanin in vitro). The pattern of changes in lead distribution caused by dithiocarbamates is consistent with the formation in the body of lipid soluble lead-dithiocarbamate complexes that pass biological barriers more easily than lead inorganic (to brain, fetus, melanocytes etc.), probably followed by a dissociation of the complexes in the tissues.
Similar articles
-
Placental transfer and fetal distribution of cadmium and mercury after treatment with dithiocarbamates.Arch Toxicol. 1984 Sep;55(3):161-7. doi: 10.1007/BF00316121. Arch Toxicol. 1984. PMID: 6093739
-
Dithiocarbamate-induced redistribution and increased brain uptake of lead in rats.Neurotoxicology. 1984 Fall;5(3):283-93. Neurotoxicology. 1984. PMID: 6097848
-
Foetal and maternal distribution of inhaled mercury vapour in pregnant mice: influence of selenite and dithiocarbamates.Pharmacol Toxicol. 1990 Sep;67(3):222-6. doi: 10.1111/j.1600-0773.1990.tb00817.x. Pharmacol Toxicol. 1990. PMID: 2175030
-
Increased lead levels in brain after long-term treatment with lead and dithiocarbamate or thiuram derivatives in rats.Acta Pharmacol Toxicol (Copenh). 1985 Apr;56(4):309-15. doi: 10.1111/j.1600-0773.1985.tb01295.x. Acta Pharmacol Toxicol (Copenh). 1985. PMID: 2992231
-
Dithiocarbamates: Challenges, Control, and Approaches to Excellent Yield, Characterization, and Their Biological Applications.Bioinorg Chem Appl. 2019 Feb 6;2019:8260496. doi: 10.1155/2019/8260496. eCollection 2019. Bioinorg Chem Appl. 2019. PMID: 30881441 Free PMC article. Review.
Cited by
-
Effect of lead on postnatal development of the bank vole (Clethrionomys glareolus).Arch Environ Contam Toxicol. 1988 May;17(3):365-71. doi: 10.1007/BF01055174. Arch Environ Contam Toxicol. 1988. PMID: 3288128 No abstract available.
-
Distribution of lead in lactating mice and suckling offspring with special emphasis on the mammary gland.Arch Toxicol. 1996;70(3-4):237-43. doi: 10.1007/s002040050266. Arch Toxicol. 1996. PMID: 8825683
-
Effect of sodium pyridinethione on the uptake and distribution of nickel in rats, ferrets and guinea-pigs.Arch Toxicol. 1994;68(7):450-8. doi: 10.1007/s002040050096. Arch Toxicol. 1994. PMID: 7979962
-
Placental transfer and fetal distribution of cadmium and mercury after treatment with dithiocarbamates.Arch Toxicol. 1984 Sep;55(3):161-7. doi: 10.1007/BF00316121. Arch Toxicol. 1984. PMID: 6093739
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources