Decreased Sperm Number and Motile Activity on the F1 Offspring Maternally Exposed to Butyl p-Hydroxybenzoic Acid(Butyl Paraben).
Open Access
- 1 January 2002
- journal article
- Published by Japanese Society of Veterinary Science in The Journal of Veterinary Medical Science
- Vol. 64 (3) , 227-235
- https://doi.org/10.1292/jvms.64.227
Abstract
Butyl p-hydroxybenzoic acid (butyl paraben, BP) is widely used as a preservative in food and cosmetic products. Routledge et al showed that BP is weakly estrogenic in both in vitro and in vivo (rat uterotrophic) analyses. We investigated whether maternal exposures to BP during gestation and lactation periods affected the development of the reproductive organs of the F1 offspring. Pregnant Sprague-Dawley rats were injected subcutaneously with 100 or 200 mg/kg of BP from gestation day (GD) 6 to postnatal day (PND) 20. In the group exposed to 200 mg/kg of BP, the proportion of pups born alive and the proportion of pups surviving to weaning were decreased. The body weights of female offspring were significantly decreased at PND 49. The weights of testes, seminal vesicles and prostate glands were significantly decreased in rats exposed to 100 mg/kg of BP on PND 49. In contrast, the weights of female reproductive organs were not affected by BP. The sperm count and the sperm motile activity in the epididymis were significantly decreased at doses of 100 and 200 mg/kg of BP. In accordance with the sperm count in the epididymis, the number of round spermatids and elongated spermatids in the seminiferous tubule (stage VII) were significantly decreased by BP. Testicular expression of estrogen receptor (ER)-α and ER-β mRNA was significantly increased in 200 mg/kg of BP treated group at PND 90. Taken together, these results indicated that maternal exposure of BP might have adverse effects on the F1 male offspring.Keywords
This publication has 43 references indexed in Scilit:
- Effect of neonatal exposure to estrogenic compounds on development of the excurrent ducts of the rat testis through puberty to adulthood.Environmental Health Perspectives, 1999
- Neonatal exposure of male rats to estradiol benzoate causes rete testis dilation and backflow impairment of spermatogenesisThe Anatomical Record, 1998
- Immunolocalisation of oestrogen receptor-α within the testis and excurrent ducts of the rat and marmoset monkey from perinatal life to adulthoodJournal of Endocrinology, 1997
- Review Article: Evaluation of Testicular Toxicity in Safety Evaluation Studies: The Appropriate Use of Spermatogenic StagingToxicologic Pathology, 1997
- Targeted disruption of the estrogen receptor gene in male mice causes alteration of spermatogenesis and infertilityEndocrinology, 1996
- Declining semen quality and increasing incidence of testicular cancer: is there a common cause?Environmental Health Perspectives, 1995
- Oestrogenic activity of an environmentally persistent alkylphenol in the reproductive tract but not the brain of rodentsThe Journal of Steroid Biochemistry and Molecular Biology, 1995
- Evidence for decreasing quality of semen during past 50 years.BMJ, 1992
- Quantitative analysis of Sertoli cells in neonatally oestrogen-treated ratsReproduction, 1987
- PrefaceJournal of the American College of Toxicology, 1984