| Cumulative Dietary Energy Intake Determines the Onset of Puberty in Female Rats Jenny Odum,1 Helen Tinwell,1 Graham Tobin,2 and John Ashby1 1Syngenta Central Toxicology Laboratory, Macclesfield, Cheshire, United Kingdom; 2Harlan Teklad UK, Bicester, Oxfordshire, United Kingdom Abstract
Laboratory animal diets for studies to determine the endocrine-disrupting potential of chemicals are under scrutiny because they can affect both assay control values and assay sensitivity. Although phytoestrogen content is important, we have previously shown that a phytoestrogen-rich diet and a phytoestrogen-free diet were equally uterotrophic to rats and advanced vaginal opening (VO) when compared with the standard diet RM1. Abolition of the effects by the gonadotrophin-releasing hormone antagonist Antarelix indicated that these effects were mediated through the hypothalamus-pituitary-reproductive organ axis. In the present study, we investigated the relationship between cumulative energy intake and sexual maturation in female rats. Infant formula (IF) at different concentrations and synthetic diets, with a wide range of metabolizable energy (ME) values, were used to modulate energy intake. Increasing energy intake was associated with an increase in uterine weight (absolute and adjusted for body weight) for both IF and the synthetic diets. In both cases, the increased uterine weight was directly proportional to energy intake. Body weight was unaffected by IF consumption but, in the case of the diets, was increased proportionally with energy consumption. Antarelix abolished the uterine weight increases with both formula and the diets, whereas body weight was unaffected. The mean day of VO was also advanced by high-ME diets and IF, whereas body weight at VO was unaffected. VO occurred at an energy intake of approximately 2,300kJ/rat determined by measuring total food intake from weaning to VO, indicating that this cumulative energy intake was the trigger for puberty. ME is therefore a critical factor in the choice of diets for endocrine disruption studies. Key words: energy intake, metabolizable energy, phytoestrogens, puberty, soy, uterotrophic assay. Environ Health Perspect 112:1472-1480 (2004) . doi:10.1289/ehp.7039 available via http://dx.doi.org/ [Online 21 July 2004]
Address correspondence to J. Ashby, Syngenta Central Toxicology Laboratory, Alderley Park, Macclesfield, Cheshire, SK10 4TJ UK. Telephone: 44-0-1625-512833. Fax: 44-0-1625-590249. E-mail: john.ashby@syngenta.com The authors are employed by Syngenta and Harlan Teklad. Received 17 February 2004 ; accepted 21 July 2004.
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