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Effects of Low-Dose Developmental Bisphenol A Exposure on Metabolic Parameters and Gene Expression in Male and Female Fischer 344 Rat Offspring
BACKGROUND: Bisphenol A (BPA) is an endocrine-disrupting chemical that may contribute to development of obesity and metabolic disorders. Humans are constantly exposed to low concentrations of BPA, and studies support that the developmental period is particularly sensitive. OBJECTIVES: The aim was to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Environmental Health Perspectives
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743697/ https://www.ncbi.nlm.nih.gov/pubmed/28657538 http://dx.doi.org/10.1289/EHP505 |
Sumario: | BACKGROUND: Bisphenol A (BPA) is an endocrine-disrupting chemical that may contribute to development of obesity and metabolic disorders. Humans are constantly exposed to low concentrations of BPA, and studies support that the developmental period is particularly sensitive. OBJECTIVES: The aim was to investigate the effects of low-dose developmental BPA exposure on metabolic parameters in male and female Fischer 344 (F344) rat offspring. METHODS: Pregnant F344 rats were exposed to BPA via their drinking water, corresponding to [Formula: see text] (BPA0.5; [Formula: see text]) or [Formula: see text] (BPA50; [Formula: see text]), from gestational day (GD) 3.5 until postnatal day (PND) 22, and controls were given vehicle ([Formula: see text]). Body weight (BW), adipose tissue, liver (weight, histology, and gene expression), heart weight, and lipid profile were investigated in the 5-wk-old offspring. RESULTS: Males and females exhibited differential susceptibility to the different doses of BPA. Developmental BPA exposure increased plasma triglyceride levels ([Formula: see text] compared with [Formula: see text] , females BPA50 [Formula: see text]; [Formula: see text] compared with [Formula: see text] , males BPA0.5 [Formula: see text]) in F344 rat offspring compared with controls. BPA exposure also increased adipocyte cell density by 122% in inguinal white adipose tissue (iWAT) of female offspring exposed to BPA0.5 compared with controls ([Formula: see text] number of adipocytes/HPF compared with [Formula: see text] number of adipocytes/HPF; [Formula: see text]) and by 123% in BPA0.5 females compared with BPA50 animals ([Formula: see text] number of adipocytes/high power field (HPF) compared with [Formula: see text] number of adipocytes/HPF; [Formula: see text]). In iWAT of male offspring, adipocyte cell density was increased by 129% in BPA50-exposed animals compared with BPA0.5-exposed animals ([Formula: see text] number of adipocytes/HPF compared with [Formula: see text] number of adipocytes/HPF; [Formula: see text]). Furthermore, the expression of genes involved in lipid and adipocyte homeostasis was significantly different between exposed animals and controls depending on the tissue, dose, and sex. CONCLUSIONS: Developmental exposure to [Formula: see text] of BPA, which is 8–10 times lower than the current preliminary EFSA (European Food Safety Authority) tolerable daily intake (TDI) of [Formula: see text] and is within the range of environmentally relevant levels, was associated with sex-specific differences in the expression of genes in adipose tissue plasma triglyceride levels in males and adipocyte cell density in females when F344 rat offspring of dams exposed to BPA at [Formula: see text] were compared with the offspring of unexposed controls. https://doi.org/10.1289/EHP505 |
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