Prevention by Tiron (sodium 4,5-dihydroxybenzene-1,3-disulfonate) of vanadate-induced developmental toxicity in mice.

Abstract

Vanadate is embryotoxic and fetotoxic in golden hamsters, mice and rats. Tiron (sodium 4,5-dihydroxybenzene-1,3-disulfonate), a chelating agent widely used in analytical chemistry, is an effective antidote in the treatment of oral or parenteral vanadate poisoning. The present study evaluated the effect of administration of Tiron on sodium metavanadate (NaVO3)-induced developmental toxicity in mice. NaVO3 (25 mg/kg, i.p.) was injected on day 12 of gestation, whereas Tiron was injected subcutaneously at 0, 24, 48, and 72 hr after NaVO3 administration. Tiron effectiveness was assessed at dosage levels of 0, 250, 500, and 1,000 mg/kg. Cesarean sections were performed on gestation day 18. All live fetuses were examined for external, internal, and skeletal malformations and variations. Amelioration by Tiron of NaVO3 developmental toxicity was evidenced by a significant decrease in the number of resorbed fetuses, an increase in the mean fetal weight, and a reduction in the incidence of the skeletal variations caused by NaVO3. According to these results, Tiron offers encouragement with regard to its therapeutic potential for pregnant women exposed to vanadate. However, further investigations, including the effect of increasing the time interval between acute vanadate exposure and initiation of Tiron therapy, are required.

• Authors: J L Domingo, M A Bosque, M Luna, J Corbella
• Journal: Teratology (Teratology) Vol. 48 Issue 2 Pg. 133-8 (Aug 1993) ISSN: 0040-3709 [Print] United States
• PMID: 8211819 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Teratogens
• Vanadates
• 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt

Topics

• 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt (pharmacology)
• Animals
• Birth Weight
• Bone and Bones (abnormalities)
• Female
• Fetal Growth Retardation
• Male
• Mice
• Teratogens (toxicity)
• Vanadates (antagonists & inhibitors, toxicity)