Butylparaben multigenerational reproductive assessment by continuous breeding in Hsd:Sprague Dawley SD rats following dietary exposure
•Public safety concerns of endocrine disruption by parabens have been on the rise.•Toxicity was assessed using multigenerational continuous breeding study design.•Increased liver weight and hepatic hypertrophy occurred in perinatally exposed rats.•Reproduction and pubertal development were unperturb...
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Veröffentlicht in: | Reproductive toxicology (Elmsford, N.Y.) N.Y.), 2020-09, Vol.96, p.258-272 |
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Sprache: | eng |
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Zusammenfassung: | •Public safety concerns of endocrine disruption by parabens have been on the rise.•Toxicity was assessed using multigenerational continuous breeding study design.•Increased liver weight and hepatic hypertrophy occurred in perinatally exposed rats.•Reproduction and pubertal development were unperturbed by butylparaben exposure.
Butylparaben (BP) is an antimicrobial agent utilized for decades as a preservative in numerous consumer products. The safety of parabens has recently come under scrutiny based on reports of estrogenic activity and suggested adverse effects upon the reproductive system. Due to the limited availability of studies that address the potential for BP exposure to induce reproductive toxicity, and clear evidence of human exposure, the National Toxicology Program conducted a multigenerational continuous breeding study to evaluate the impact of dietary BP-exposure at 0, 5000, 15,000, or 40,000 ppm on reproductive and developmental parameters in Hsd:Sprague Dawley SD rats. BP-exposure was not associated with adverse alterations of fertility, fecundity, pubertal attainment, or reproductive parameters in F0, F1, or F2 generations. Exposure-dependent increases in liver weights, and incidences of non-neoplastic liver lesions suggest the liver is a target organ of BP toxicity. No findings were observed that would support the purported mechanism of BP-induced endocrine disruption in perinatally-exposed rodents. |
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ISSN: | 0890-6238 1873-1708 |
DOI: | 10.1016/j.reprotox.2020.07.006 |