n-Butylparaben exposure through gestation and lactation impairs spermatogenesis and steroidogenesis causing reduced fertility in the F1 generation male rats.
Animals
Dose-Response Relationship, Drug
Endocrine Disruptors
/ toxicity
Female
Fertility
/ drug effects
Gene Expression Regulation, Developmental
/ drug effects
Lactation
Leydig Cells
/ drug effects
Male
Parabens
/ toxicity
Pregnancy
Prenatal Exposure Delayed Effects
/ chemically induced
Rats
Receptors, Steroid
/ genetics
Sexual Maturation
/ drug effects
Sperm Count
Spermatogenesis
/ drug effects
Spermatozoa
/ drug effects
Testis
/ drug effects
Endocrine disruptors
Fertility
Gestation and lactational exposure
Puberty
Spermatogenesis
Steroidogenesis
n-Butylparaben
Journal
Environmental pollution (Barking, Essex : 1987)
ISSN: 1873-6424
Titre abrégé: Environ Pollut
Pays: England
ID NLM: 8804476
Informations de publication
Date de publication:
Jan 2020
Jan 2020
Historique:
received:
01
04
2019
revised:
23
07
2019
accepted:
23
07
2019
pubmed:
2
11
2019
medline:
23
2
2020
entrez:
2
11
2019
Statut:
ppublish
Résumé
Parabens are class of preservatives used in vast majority of commercial products, and a potential Endocrine Disrupting Chemical (EDC). The present study was undertaken to delineate the effects of n-butylparaben on F1 male progeny exposed maternally through gestation and lactation via subcutaneous route. The F0 dams were given subcutaneous injections of n-butylparaben from gestation day (GD) 6 to postnatal day (PND) 21 with doses of 10, 100, 1000 mg/kg Bw/day in corn oil. The F1 male rats were monitored for pubertal development and sexual maturation; these were sacrificed on PND 30, 45 and 75. On PND 75, these F1 male rats were subjected for fertility assessment with unexposed female rats. A delayed testicular descent at 100 and 1000 mg/kg Bw dose and delayed preputial separation at 10 mg/kg Bw dose was observed in exposed F1 male rats. Decreased sperm count, motility and Daily Sperm Production was observed at 100 mg/kg Bw dose at PND 75. Interestingly, the sperm transit time in the epididymis was accelerated at this dose. Significant perturbed testicular expression of steroid receptors (ERα and β, AR), INSL3 and StAR genes with increased T and LH levels indicates direct effect on spermatogenesis and steroidogenesis. These F1 generation adult rats were sub-fertile with increased (%) pre- and post-implantation loss at 100 and 1000 mg/kg Bw/day dose. This is the first report on n-butylparaben highlighting the involvement of testicular leydig cells with accelerated sperm transit time leading to reduced fertility in the maternally exposed F1 male rats through estrogenic/anti-androgenic action.
Identifiants
pubmed: 31672375
pii: S0269-7491(19)31684-7
doi: 10.1016/j.envpol.2019.112957
pii:
doi:
Substances chimiques
Endocrine Disruptors
0
Parabens
0
Receptors, Steroid
0
butylparaben
3QPI1U3FV8
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
112957Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.