Bisphenol AP is anti-estrogenic and may cause adverse effects at low doses relevant to human exposure.

A recent increase in the use of bisphenol A (BPA) alternatives to manufacture plastics has led to safety concerns. Here, we evaluated the estrogenic and anti-estrogenic activities of bisphenol AP (BPAP), a poorly studied BPA alternative, using in vitro, in vivo and in silico tools. BPAP exhibited weak estrogenicity but strong anti-estrogenicity (IC ₅₀  = 2.35 μM) in a GeneBLAzer™ β-lactamase reporter gene assay. BPAP, when administered alone or in combination with E ₂ (50 μg kg ^-1 bw d ^-1 ) for 3 d, significantly decreased the uterine weights of post-weaning CD-1 mice at doses of 10 mg kg ^-1 bw d ^-1 and higher. When administered alone to prepubertal CD-1 mice for 10 d, BPAP significantly decreased the uterine weights at doses of 80 μg kg ^-1 bw d ^-1 and higher. Toxicogenomic analysis showed that BPAP regulated an opposite patterns of gene expression than that of E ₂ in mouse uteri. In a glucose tolerance test using male mice, BPAP was found to disrupt the blood glucose homeostasis at low doses relevant to human exposure (1 and 100 μg kg ^-1 bw d ^-1 ). Our results suggest that BPAP should be of great concern which might affect the sexual development in immature feminine and disrupt the blood glucose homeostasis at very low doses.
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