Effect of Central Injection of Neostigmine on the Bacterial Endotoxin Induced Suppression of GnRH/LH Secretion in Ewes during the Follicular Phase of the Estrous Cycle

Int J Mol Sci. 2019 Sep 17;20(18):4598. doi: 10.3390/ijms20184598.

Abstract

Induced by a bacterial infection, an immune/inflammatory challenge is a potent negative regulator of the reproduction process in females. The reduction of the synthesis of pro-inflammatory cytokine is considered as an effective strategy in the treatment of inflammatory induced neuroendocrine disorders. Therefore, the effect of direct administration of acetylcholinesterase inhibitor-neostigmine-into the third ventricle of the brain on the gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) secretions under basal and immune stress conditions was evaluated in this study. In the study, 24 adult, 2-years-old Blackhead ewes during the follicular phase of their estrous cycle were used. Immune stress was induced by the intravenous injection of LPS Escherichia coli in a dose of 400 ng/kg. Animals received an intracerebroventricular injection of neostigmine (1 mg/animal) 0.5 h before LPS/saline treatment. It was shown that central administration of neostigmine might prevent the inflammatory-dependent decrease of GnRH/LH secretion in ewes and it had a stimulatory effect on LH release. This central action of neostigmine is connected with its inhibitory action on local pro-inflammatory cytokines, such as interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)α synthesis in the hypothalamus, which indicates the importance of this mediator in the inhibition of GnRH secretion during acute inflammation.

Keywords: GnRH; cytokines; inflammation; luteinizing hormone; neostigmine; reproduction disorders.

MeSH terms

  • Cholinesterase Inhibitors / administration & dosage*
  • Endotoxins / adverse effects*
  • Estrous Cycle / drug effects*
  • Estrous Cycle / metabolism*
  • Follicular Phase / drug effects
  • Follicular Phase / metabolism
  • Gonadotropin-Releasing Hormone / biosynthesis*
  • Hydrocortisone / biosynthesis
  • Hypothalamus / metabolism
  • Lipopolysaccharides / adverse effects
  • Luteinizing Hormone / biosynthesis*
  • Neostigmine / administration & dosage*
  • alpha7 Nicotinic Acetylcholine Receptor / metabolism

Substances

  • Cholinesterase Inhibitors
  • Endotoxins
  • Lipopolysaccharides
  • alpha7 Nicotinic Acetylcholine Receptor
  • Gonadotropin-Releasing Hormone
  • Neostigmine
  • Luteinizing Hormone
  • Hydrocortisone