Perfluorooctane sulfonate impairs rat Leydig cell development during puberty

Chemosphere. 2018 Jan:190:43-53. doi: 10.1016/j.chemosphere.2017.09.116. Epub 2017 Sep 26.

Abstract

Perfluorooctane sulfonate (PFOS) possibly delays male sexual development. However, its effects on pubertal Leydig cell development are unclear. The objective of the present study was to investigate the effects of in vivo PFOS exposure on rat Leydig cell development during puberty. Immature male Sprague Dawley rats were gavaged 5 or 10 mg/kg PFOS on postnatal day 35 for 21 days. Compared to the control (0 mg/kg), PFOS lowered serum testosterone levels without altering luteinizing hormone and follicle-stimulating hormone levels on postnatal day 56. PFOS in vivo downregulated mRNA or protein levels of Leydig cells (Lhcgr, Cyp11a1, and Cyp17a1). PFOS in vitro inhibited androgen secretion in immature Leydig cells at ≥ 50 nM, most possibly via downregulating Hsd17b3 mRNA level. At ≥ 500 nM, PFOS downregulated Lhcgr, inhibited BCL-2 and increased BAX levels to cause Leydig cell apoptosis. In conclusion, PFOS at a lower dose directly inhibited pubertal development of Leydig cells.

Keywords: Leydig cell development; Leydig cells; Perfluorooctane sulfonate; Rat; Testis.

MeSH terms

  • Alkanesulfonic Acids / toxicity*
  • Animals
  • Apoptosis / drug effects
  • Down-Regulation
  • Fluorocarbons / toxicity*
  • Leydig Cells / drug effects*
  • Leydig Cells / pathology
  • Luteinizing Hormone / drug effects
  • Luteinizing Hormone / metabolism
  • Male
  • Proteins / drug effects
  • Proteins / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sexual Maturation / drug effects*
  • Testosterone / blood

Substances

  • Alkanesulfonic Acids
  • Fluorocarbons
  • Proteins
  • RNA, Messenger
  • Testosterone
  • Luteinizing Hormone
  • perfluorooctane sulfonic acid