Effects of melatonin on development and hormone secretion of sheep theca cells in vitro

Theriogenology. 2023 Mar 1:198:172-182. doi: 10.1016/j.theriogenology.2022.12.036. Epub 2022 Dec 27.

Abstract

Theca cells (TCs) play a unique role in the structure and function of the ovary. They are not only the structural basis of the follicle but also the androgen-secreting cells in female mammals, which can affect the normal development and atresia of the follicle. The results showed that melatonin receptor (MTR) MT1 and MT2 were expressed on sheep TCs. In the present study, the effects of different concentrations of MT at 0, 10-10, 10-8, 10-6 and 10-4 M/L on sheep TCs with regards to the antioxidant levels, proliferation, apoptosis and steroid hormone secretion were investigated. The results showed that in sheep TCs, all concentrations of MT significantly decreased reactive oxygen species (ROS) concentration and BAX expression; increased Cat, Sod1, and BCL-2 expression. The proliferation viability of TCs was significantly inhibited in all groups except for 10-10 M/L MT, and the expression of cyclin D1 and CDK4 was significantly reduced. MT significantly increased StAR expression and progesterone secretion in TCs, but there was no significant effect on androgen secretion and CYP11A1, CYP17A1 and 3β-HSD expression in all groups. MT-induced progesterone secretion was completely inhibited by Luzindole (a nonspecific MT1 and MT2 inhibitor) and partially inhibited by 4p-PDOT (specific MT2 inhibitor). MT-induced progesterone secretion can be inhibited by LY294002 (PI3K/AKT pathway inhibitor). This study indicated that MT inhibits apoptosis and proliferation of in vitro cultured sheep TCs, which has implications for slowing ovarian atresia and aging. MT activates the PI3K/Akt pathway to mediate the synthesis and secretion of progesterone by TCs. This study provides a basis for further exploration of the role of TCs on follicle development and ovarian steroid hormone secretion.

Keywords: Apoptosis; Hormone secretion; Melatonin; Proliferation; Theca cells.

MeSH terms

  • Androgens / metabolism
  • Animals
  • Female
  • Mammals
  • Melatonin* / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Progesterone / pharmacology
  • Proto-Oncogene Proteins c-akt / metabolism
  • Receptor, Melatonin, MT2 / metabolism
  • Sheep
  • Theca Cells

Substances

  • Melatonin
  • Progesterone
  • Proto-Oncogene Proteins c-akt
  • Androgens
  • Phosphatidylinositol 3-Kinases
  • Receptor, Melatonin, MT2