Low doses of dietary lead are associated with a profound reduction in the time to the onset of puberty in female mice

• Published in: Reproductive toxicology (Elmsford, N.Y.) Vol. 22; no. 4; pp. 586 - 590
• Main Authors: Iavicoli, I., Carelli, G., Stanek, E.J., Castellino, N., Li, Z., Calabrese, E.J.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01-11-2006; Elsevier
• Subjects: Administration, Oral; Animals; Biological and medical sciences; Chemical and industrial products toxicology. Toxic occupational diseases; Diet; Dose-Response Relationship, Drug; Dose–response; Embryology: invertebrates and vertebrates. Teratology; Estrus - blood; Estrus - drug effects; Female; Female reproduction; Fertility - drug effects; Fundamental and applied biological sciences. Psychology; Lead; Lead - administration & dosage; Lead - blood; Lead - toxicity; Litter Size - drug effects; Low dose; Male; Medical sciences; Metals and various inorganic compounds; Mice; Nesting Behavior - drug effects; Opposite effects; Puberty; Reproduction - drug effects; Sex Factors; Sexual Maturation - drug effects; Sexual Maturation - physiology; Teratology. Teratogens; Time Factors; Toxicology; Vagina - drug effects; Lead; Opposite effects; Puberty; Dose–response; Female reproduction; Low dose; Nutrition; Rodentia; Oral administration; Feeding; Heavy metal; Dose activity relation; Vertebrata; Reproduction; Reduction; Mammalia; Age of onset; Diet; Mouse; Animal; Female; Dose-response
• ISSN: 0890-6238; 1873-1708
• DOI: 10.1016/j.reprotox.2006.03.016

We report results from a replication in second and third generation female mice of accelerated time to puberty associated with low Pb exposure levels
[1]. Mice in the 2nd generation study are offspring of mice from the initial study; the 3rd generation mice are offspring from mice in the 2nd generation study. For each generation the time to puberty onset was markedly influenced by exposure to dietary lead. Modest increases in blood lead concentration from a normal background of 2–3 to 8–13
μg/dl delayed the onset of puberty by 10–20% from a normal of 33–35 days to about 40–43 days; reducing blood lead from 2–3 to 0.7
μg/dl was associated with profound acceleration of puberty to 21 days, an enhancement by over 30%. This dose–response relationship, which replicates previous novel findings, has possible ecological as well as public health significance and indicates that lead is able to induce biologically significant changes at blood lead levels previously thought to be without effect.