Carbon Black Nanoparticles Selectively Alter Follicle-Stimulating Hormone Expression in vitro and in vivo in Female

Charlotte Avet1, Emmanuel N Paul2, Ghislaine Garrel1

  • 1Université de Paris, BFA, UMR 8251, CNRS, ERL U1133, Inserm, Paris, France.

Frontiers in Neuroscience
|December 23, 2021
PubMed

Insights

Carbon black nanoparticles (CB NPs) exposure in female mice increases follicle-stimulating hormone (FSH) levels and gene expression without affecting luteinizing hormone (LH), potentially causing gonadotropin imbalance.

Area of Science:

  • Toxicology
  • Reproductive Endocrinology
  • Nanotechnology

Background:

  • Nanoparticle toxicity impacts female reproductive health, but mechanisms require clarification.
  • Pituitary gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), regulate reproductive functions.
  • Carbon black nanoparticles (CB NPs) are prevalent in occupational settings.

Purpose of the Study:

  • To investigate the effects of CB NPs on pituitary gonadotropins (LH and FSH) in female mice.
  • To elucidate the underlying mechanisms of CB NP action on gonadotropin regulation.

Main Methods:

  • Adult female mice were exposed to CB NPs via intratracheal administration over 4 weeks.
  • In vitro studies used primary pituitary cell cultures and the LβT2 gonadotrope cell line.
  • Circulating hormone levels, gene expression (Fshb), and cell signaling pathways (cAMP/PKA) were analyzed.

Main Results:

  • CB NP exposure did not disrupt estrous cyclicity but increased circulating FSH and pituitary Fshb expression.
  • CB NPs dose-dependently upregulated FSH, but not LH, gene expression and release in pituitary and LβT2 cells.
  • CB NPs enhanced GnRH's stimulatory effect on Fshb expression and activated the cAMP/PKA pathway in LβT2 cells.

Conclusions:

  • Occupational exposure to CB NPs alters FSH but not LH expression in female mice.
  • CB NPs may lead to gonadotropin imbalance through the cAMP/PKA signaling pathway.
  • Further research is needed to understand the full reproductive health implications of CB NP exposure.

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