The endogenous hydrogen sulfide generating system regulates ovulation

Free Radic Biol Med. 2019 Jul:138:43-52. doi: 10.1016/j.freeradbiomed.2019.03.028. Epub 2019 Mar 28.

Abstract

The generation of free-radicals such as nitric oxide has been implicated in the regulation of ovarian function, including ovulation. Tissues that generate nitric oxide typically generate another free-radical gas, hydrogen sulfide (H2S), although little is known about the role of H2S in ovarian function. The hypothesis of this study was that H2S regulates ovulation. Treatment with luteinizing hormone (LH) increased the levels of mRNA and protein of the H2S generating enzyme cystathionine γ-lyase (CTH) in granulosa cells of mice and humans in vivo and in vitro. Pharmacological inhibition of H2S generating enzymes reduced the number of follicles ovulating in mice in vivo and in vitro, and this inhibitory action was reversed by cotreatment with a H2S donor. Addition of a H2S donor to cultured mouse granulosa cells increased basal and LH-dependent abundance of mRNA encoding amphiregulin, betacellulin and tumor necrosis alpha induced protein 6, proteins important for cumulus expansion and follicle rupture. Inhibition of CTH activity reduced abundance of mRNA encoding matrix metalloproteinase-2 and -9 and tissue-type plasminogen activator, and cotreatment with the H2S donor increased the levels of these mRNA above those stimulated by LH alone. We conclude that the H2S generating system plays an important role in the propagation of the preovulatory cascade and rupture of the follicle at ovulation.

Keywords: Follicle; Granulosa cells; Ovary; Ovulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphiregulin / genetics
  • Amphiregulin / metabolism
  • Animals
  • Betacellulin / genetics
  • Betacellulin / metabolism
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Cell Size
  • Chorionic Gonadotropin / pharmacology
  • Cystathionine gamma-Lyase / genetics*
  • Cystathionine gamma-Lyase / metabolism
  • Enzyme Inhibitors / pharmacology
  • Female
  • Gene Expression Regulation / drug effects*
  • Granulosa Cells / cytology
  • Granulosa Cells / drug effects*
  • Granulosa Cells / metabolism
  • Humans
  • Hydrogen Sulfide / agonists
  • Hydrogen Sulfide / metabolism*
  • Hydroxylamine / pharmacology
  • Luteinizing Hormone / pharmacology
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nitric Oxide / metabolism
  • Ovulation / drug effects*
  • Ovulation / physiology
  • Primary Cell Culture
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Signal Transduction
  • Sulfides / pharmacology*
  • Tissue Plasminogen Activator / genetics
  • Tissue Plasminogen Activator / metabolism

Substances

  • AREG protein, human
  • Amphiregulin
  • BTC protein, human
  • Betacellulin
  • Cell Adhesion Molecules
  • Chorionic Gonadotropin
  • Enzyme Inhibitors
  • RNA, Messenger
  • Sulfides
  • TNFAIP6 protein, human
  • Hydroxylamine
  • Nitric Oxide
  • Luteinizing Hormone
  • Tissue Plasminogen Activator
  • MMP2 protein, human
  • Matrix Metalloproteinase 2
  • MMP9 protein, human
  • Matrix Metalloproteinase 9
  • Cystathionine gamma-Lyase
  • sodium bisulfide
  • Hydrogen Sulfide