Betamethasone causes intergenerational reproductive impairment in male rats

• Published in: Reproductive toxicology (Elmsford, N.Y.) Vol. 71; pp. 108 - 117
• Main Authors: Borges, Cibele dos Santos, Pacheco, Taina Louise, da Silva, Katiussia Pinho, Fernandes, Fábio Henrique, Gregory, Mary, Pupo, André Sampaio, Salvadori, Daisy Maria F., Cyr, Daniel G., Kempinas, Wilma De G.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.08.2017
• Subjects: Animals; Betamethasone - toxicity; Betamethasone intergenerational effects; DNA Fragmentation; Female; Fertility; Fertility - drug effects; Glucocorticoids - toxicity; Life Sciences; Male; Pregnancy; Prenatal Exposure Delayed Effects; Puberty onset; Rats, Wistar; Reproduction - drug effects; Seminal vesicle contractility; Seminal Vesicles - drug effects; Seminal Vesicles - physiology; Sexual Behavior, Animal - drug effects; Sperm Count; Sperm Motility - drug effects; Sperm quality; Spermatozoa - drug effects; Testis - drug effects; Testis - metabolism; Testis - pathology; Sperm quality; Seminal vesicle contractility; Betamethasone intergenerational effects; Puberty onset; Fertility
• ISSN: 0890-6238; 1873-1708; 1873-1708
• DOI: 10.1016/j.reprotox.2017.04.012

•Betamethasone (BM) induces Hypothalamus-Pituitary-Gonadal axis disorders in F2 rats.•There was puberty onset delay and reduction in Leydig cells volume and function.•Impairment of sexual behavior and contractility of seminal vesicle.•Ιncreased DNA damage and decreased sperm quality and male fertility in F2 rats.•BM treatment causes intergenerational reproductive effects. Prenatal betamethasone (BM) exposure in rats negatively impacts sperm quality and male fertility. Studies have shown that BM can cause multi-generational effects on the pituitary-adrenal-axis of rats. The objective of this study was to assess the reproductive development and fertility of male rats (F2) whose fathers (F1) were exposed to BM (0.1mg/kg) on gestational days 12, 13, 18 and 19. In F2 rats, there was a significant reduction in body weights of the BM-treated group at PND 1 as well as delayed onset of puberty, and decreases in FSH levels, Leydig cell volume, sperm number and motility, seminal vesicle contractility and ejaculated volume. Furthermore, increased serum LH levels, sperm DNA damage and abnormal morphology were observed, resulting in reduced fertility. In conclusion, prenatal BM-treatment leads to intergenerational long-term reproductive impairment in male rats, raising concern regarding the widespread use of BM in preterm births.