Organic and Inorganic Mercury in Neonatal Rat Brain after Prenatal Exposure to Methylmercury and Mercury Vapor

• Published in: Environmental health perspectives 2010-02, Vol.118 (2), p.242-248
• Main Authors: Ishitobi, Hiromi, Stern, Sander, Thurston, Sally W., Zareba, Grazyna, Langdon, Margaret, Gelein, Robert, Weiss, Bernard
• Format: Article
• Language: English
• Subjects: Animals; Animals, Newborn; Biological and medical sciences; Blood; Body weight; Brain; Brain - metabolism; Breeding; Chemical and industrial products toxicology. Toxic occupational diseases; Chemical hazards; Dosage; Female; Fetus; Health aspects; Medical sciences; Mercury - adverse effects; Mercury - metabolism; Metals and various inorganic compounds; Methylmercury; Methylmercury Compounds - adverse effects; Methylmercury Compounds - metabolism; Physiological aspects; Pregnancy; Prenatal exposure; Prenatal Exposure Delayed Effects - metabolism; Rats; Rats, Long-Evans; Toxicity; Toxicology; Vapors
• ISSN: 0091-6765; 1552-9924
• DOI: 10.1289/ehp.0900956

Background: Many populations are exposed to multiple species of mercury (Hg), predominantly organic Hg as methylmercury (MeHg) from fish, and inorganic Hg as Hg vapor from dental amalgams. Most of our knowledge of the neurotoxicity of Hg is based on research devoted to studying only one form at a time, mostly MeHg. Objectives: In this study we investigated the effects of prenatal exposure to MeHg and Hg vapor on Hg concentrations in the brain of neonatal rats. Methods: Female Long-Evans hooded rats were exposed to MeHg (0, 3, 6, or 9 ppm as drinking solution), Hg vapor (0, 300, or 1,000 μg/m³ for 2 hr/day), or the combination of both, from 30 days before breeding through gestational day 18. On postnatal day 4, whole brains were taken from one male and one female from each of four litters in each treatment group to assess organic and inorganic Hg in the brain by cold vapor atomic absorption spectrometry. Results: Statistical analysis using linear mixed effects models showed that MeHg dose was the primary determinant of both organic and inorganic brain Hg levels. For both outcomes, we also found significant interactions between MeHg and Hg vapor exposure. These interactions were driven by the fact that among animals not exposed to MeHg, animals exposed to Hg vapor had significantly greater organic and inorganic brain Hg levels than did unexposed animals. Conclusion: This interaction, heretofore not reported, suggests that coexposure to MeHg and Hg vapor at levels relevant to human exposure might elevate neurotoxic risks.