Juvenile Toxicity Rodent Model to Study Toxicological Effects of Bisphenol A (BPA) at Dose Levels Derived From Italian Children Biomonitoring Study

Toxicol Sci. 2020 Feb 1;173(2):387-401. doi: 10.1093/toxsci/kfz226.

Abstract

Bisphenol A (BPA) is a plasticizer with endocrine disrupting properties particularly relevant for children health. Recently BPA has been associated with metabolic dysfunctions but no data are yet available in specific, long-term studies. This study aimed to evaluate BPA modes of action and hazards during animal juvenile life-stage, corresponding to childhood. Immature Sprague-Dawley rats of both sexes were orally treated with 0 (vehicle only-olive oil), 2, 6, and 18 mg/kg bw per day of BPA for 28 days, from weaning to sexual maturity. Dose levels were obtained from the PERSUADED biomonitoring study in Italian children. Both no-observed-adverse-effect-level (NOAEL)/low-observed-adverse-effect-level (LOAEL) and estimated benchmark dose (BMD) approaches were applied. General toxicity, parameters of sexual development, endocrine/reproductive/functional liver and kidney biomarkers, histopathology of target tissues, and gene expression in hypothalamic-pituitary area and liver were studied. No mortality or general toxicity occurred. Sex-specific alterations were observed in liver, thyroid, spleen, leptin/adiponectin serum levels, and hypothalamic-pituitary gene expression. Thyroid homeostasis and liver were the most sensitive targets of BPA exposure in the peripubertal phase. The proposed LOAEL was 2 mg/kg bw, considering as critical effect the liver endpoints, kidney weight in male and adrenal histomorphometrical alterations and osteopontin upregulation in female rats. The BMD lower bounds were 0.05 and 1.33 mg/kg bw in males and females, considering liver and thyroid biomarkers, respectively. Overall, BPA evaluation at dose levels derived from children biomonitoring study allowed to identify sex-specific, targeted toxicological effects that may have significant impact on risk assessment for children.

Keywords: benchmark dose; food contaminant; hazard characterization; low-observed-adverse-effect-level; sex-related effects.

MeSH terms

  • Adiponectin
  • Administration, Oral
  • Adrenal Glands
  • Age Factors
  • Animals
  • Benzhydryl Compounds / analysis
  • Benzhydryl Compounds / blood
  • Benzhydryl Compounds / toxicity*
  • Biological Monitoring
  • Biomarkers / blood
  • Body Weight / drug effects
  • Endocrine Disruptors / toxicity
  • Female
  • Gene Expression
  • Genitalia
  • Hormones / analysis*
  • Hormones / blood*
  • Hypothalamo-Hypophyseal System
  • Liver
  • Male
  • Pancreas
  • Phenols / analysis
  • Phenols / blood
  • Phenols / toxicity*
  • Rats, Sprague-Dawley
  • Spleen
  • Thyroid Gland

Substances

  • Adiponectin
  • Benzhydryl Compounds
  • Biomarkers
  • Endocrine Disruptors
  • Hormones
  • Phenols
  • bisphenol A