» Articles » PMID: 34632005

Gestational and Lactational Exposure to BPA or BPS Has Minimal Effects on Skeletal Outcomes in Adult Female Mice

Overview
Journal Bone Rep
Date 2021 Oct 11
PMID 34632005
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Bisphenol-A (BPA) and bisphenol-S (BPS) are estrogen disrupting chemicals (EDCs) found in the environment and common household items. Estrogen is a primary hormonal regulator of bone growth and development; however, the impact of gestational BPA or BPS exposure on skeletal health of offspring remains relatively unknown. In this longitudinal study, adult female mice were randomized into three groups: 200 μg BPA/kg BW (BPA), 200 μg BPS/kg BW (BPS) or control (CON). Animals in each group were further randomized to exercise treatment (EX) or sedentary (SED) control, resulting in six overall groups. BPA/BPS/CON and EX/SED treatment were initiated prior to mating and continued through mating, gestation, and lactation. One female offspring from each dam ( = 6/group) was assessed at 17 weeks of age to evaluate effects of EDC exposure on the adult skeleton. Cortical geometry of the mid-diaphysis and trabecular microarchitecture of the distal femur were assessed via micro-computed tomography. Biomechanical strength and mineral apposition rate of the femoral diaphysis were assessed via three-point bending and dynamic histomorphometry, respectively. Sclerostin expression was measured using immunohistochemistry. Two-factor ANOVA or ANCOVA were used to determine the effects of maternal exercise and BPA or BPS exposure on trabecular and cortical bone outcomes, respectively. Consistent with prior studies, there were no significant differences in body weight, femoral length, cortical geometry, trabecular microarchitecture, or biomechanical strength between groups in female offspring. In conclusion, gestational BPA exposure and maternal exercise have minimal impact on skeletal outcomes in female adult offspring.

Citing Articles

Prenatal and Neonatal Bone Health: Updated Review on Early Identification of Newborns at High Risk for Osteopenia.

Perrone S, Caporilli C, Grassi F, Ferrocino M, Biagi E, DellOrto V Nutrients. 2023; 15(16).

PMID: 37630705 PMC: 10459154. DOI: 10.3390/nu15163515.


Skeletal effects following developmental flame-retardant exposure are specific to sex and chemical class in the adult Wistar rat.

Schkoda S, Horman B, Witchey S, Jansson A, Macari S, Patisaul H Front Toxicol. 2023; 5:1216388.

PMID: 37577032 PMC: 10414991. DOI: 10.3389/ftox.2023.1216388.


Experimental Exposure to Bisphenol A Has Minimal Effects on Bone Tissue in Growing Rams-A Preliminary Study.

Brankovic J, Leskovec J, Sturm S, Cerkvenik-Flajs V, Sterpin S, Osredkar J Animals (Basel). 2022; 12(17).

PMID: 36077899 PMC: 9454980. DOI: 10.3390/ani12172179.

References
1.
Mao J, Jain A, Denslow N, Nouri M, Chen S, Wang T . Bisphenol A and bisphenol S disruptions of the mouse placenta and potential effects on the placenta-brain axis. Proc Natl Acad Sci U S A. 2020; 117(9):4642-4652. PMC: 7060676. DOI: 10.1073/pnas.1919563117. View

2.
Doube M . The Ellipsoid Factor for Quantification of Rods, Plates, and Intermediate Forms in 3D Geometries. Front Endocrinol (Lausanne). 2015; 6:15. PMC: 4329874. DOI: 10.3389/fendo.2015.00015. View

3.
Pereira M, Gohin S, Lund N, Hvid A, Smitham P, Oddy M . Sclerostin does not play a major role in the pathogenesis of skeletal complications in type 2 diabetes mellitus. Osteoporos Int. 2016; 28(1):309-320. PMC: 5206261. DOI: 10.1007/s00198-016-3718-0. View

4.
Chen X, Wang Z, Duan N, Zhu G, Schwarz E, Xie C . Osteoblast-osteoclast interactions. Connect Tissue Res. 2017; 59(2):99-107. PMC: 5612831. DOI: 10.1080/03008207.2017.1290085. View

5.
Diel P, Schulz T, Smolnikar K, Strunck E, Vollmer G, Michna H . Ability of xeno- and phytoestrogens to modulate expression of estrogen-sensitive genes in rat uterus: estrogenicity profiles and uterotropic activity. J Steroid Biochem Mol Biol. 2000; 73(1-2):1-10. DOI: 10.1016/s0960-0760(00)00051-0. View