Neuroendocrine and behavioral effects of maternal exposure to oral bisphenol A in female mice

• Published in: Journal of endocrinology Vol. 220; no. 3; pp. 375 - 388
• Main Authors: Naulé, Lydie, Picot, Marie, Martini, Mariangela, Parmentier, Caroline, Hardin-Pouzet, Hélène, Keller, Matthieu, Franceschini, Isabelle, Mhaouty-Kodja, Sakina
• Format: Journal Article
• Language: English
• Published: England BioScientifica 01-03-2014
• Subjects: Animals; Benzhydryl Compounds - adverse effects; Estradiol - metabolism; Female; Humans; Life Sciences; Male; Maternal Exposure - adverse effects; Mice; Mice, Inbred C57BL; Neurosecretory Systems - drug effects; Neurosecretory Systems - metabolism; Other; Ovary - growth & development; Ovary - metabolism; Phenols - adverse effects; Pregnancy; Prenatal Exposure Delayed Effects - etiology; Prenatal Exposure Delayed Effects - metabolism; Prenatal Exposure Delayed Effects - psychology; Preoptic Area - drug effects; Sexual Behavior, Animal - drug effects; Uterus - growth & development; Uterus - metabolism; bisphenol A; nervous system; female mice; behaviors; kisspeptin; reproduction; bisphenol a; behavior
• ISSN: 0022-0795; 1479-6805
• DOI: 10.1530/JOE-13-0607

Bisphenol A (BPA) is a widespread estrogenic compound. We investigated the effects of maternal exposure to BPA at reference doses on sexual behavior and neuroendocrine functions of female offspring in C57BL/6J mice. The dams were orally exposed to vehicle alone or vehicle-containing BPA at doses equivalent to the no observed adverse effect level (5 mg/kg body weight per day) and tolerable daily intake (TDI, 0.05 mg/kg body weight per day) level from gestational day 15 until weaning. Developmental exposure to BPA increased the lordosis quotient in naive females exposed to BPA at the TDI dose only. BPA exposure had no effect on olfactory preference, ability to express masculine behaviors or number of calbindin-positive cells, a sexually dimorphic population of the preoptic area. BPA at both doses selectively increased kisspeptin cell number in the preoptic periventricular nucleus of the rostral periventricular area of the third ventricle in adult females. It did not affect the number of GNRH-positive cells or percentage of kisspeptin appositions on GNRH neurons in the preoptic area. These changes were associated with higher levels of estradiol (E2) at the TDI dose while levels of LH, estrus cyclicity, ovarian and uterine weights, and fertility remained unaffected. Delay in the time of vaginal opening was observed during the postnatal period at TDI dose, without any alteration in body growth. This shows that developmental exposure to BPA at reference doses did not masculinize and defeminize the neural circuitry underlying sexual behavior in female mice. The TDI dose specifically exacerbated responses normally induced by ovarian E2, through estrogen receptor α, during the postnatal/prepubertal period.