Multiple dexamethasone treatment affects morphometric parameters of gonadotrophic cells in adult female rats

N Negić1, N Nestorović, M Manojlović-Stojanoski

  • 1Institute for Biological Research Sinisa Stanković, Belgrade, Serbia and Montenegro. negicn@ibiss.bg.ac.yu

Insights

Dexamethasone (Dx) treatment in female rats altered pituitary gonadotrophic cells. This study observed significant changes in luteinizing hormone (LH) and follicle-stimulating hormone (FSH) cell volume and number, impacting reproductive function.

Area of Science:

  • Endocrinology
  • Reproductive Biology
  • Cell Biology

Background:

  • Glucocorticoids, such as dexamethasone (Dx), are known to affect various biological systems.
  • The reproductive system is particularly sensitive to hormonal fluctuations, including those induced by glucocorticoids.

Purpose of the Study:

  • To investigate the impact of dexamethasone (Dx) treatment on the histological and morphometric characteristics of pituitary gonadotrophic cells (LH and FSH cells) in adult female rats.

Main Methods:

  • Adult female Wistar rats were administered dexamethasone (Dx) over three consecutive days.
  • Pituitary glands were collected 24 and 72 hours post-treatment for analysis.
  • Peroxidase-anti-peroxidase (PAP) immunocytochemistry was employed to study LH and FSH cells.
  • Stereological and morphometric analyses were performed to quantify cellular changes.

Main Results:

  • Dexamethasone (Dx) treatment significantly reduced the volume of LH cells and their nuclei at both 24 and 72 hours post-injection.
  • The volume density of LH cells increased at 24 hours but normalized by 72 hours.
  • The number of LH cells per unit area significantly increased at both time points.
  • FSH cells exhibited similar changes to LH cells, with a notable sustained increase in volume density.

Conclusions:

  • Dexamethasone (Dx) significantly alters the immunocytochemical and morphometric features of pituitary gonadotrophic (LH and FSH) cells in female rats.
  • These observed changes suggest a potential disruption of reproductive hormone regulation following glucocorticoid exposure.

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