Abstract

Gonadotropin releasing hormone (GnRH) neurons provide neuronal input to the preoptic area (POA) and the arcuate nucleus (Arc), two regions involved critically in the regulation of neuroendocrine functions and associated behaviors. These areas contain tyrosine hydroxylase immunoreactive (TH-IR) neurons, which play location-specific roles in the neuroendocrine control of both the luteinizing hormone and prolactin secretion, as well as, sexually motivated behaviors. Concerning changes in the activity of GnRH neurons and the secretion pattern of GnRH seen under the influence of rising serum estrogen levels and during lactation, we tested the hypothesis that the functional state of GnRH neurons is mediated via direct synaptic connections to TH-IR neurons in the POA and Arc. In addition, we examined putative changes of these inputs in lactating mice and in mothers separated from their pups. Confocal microscopic and pre-embedding immunohistochemical studies on ovariectomized mice treated with 17β-estradiol (OVX+E2) provided evidence for direct appositions and asymmetric synapses between GnRH-IR fiber varicosities and TH-IR neurons in the POA and the Arc. As TH co-localizes with kisspeptin (KP) in the POA, confocal microscopic analysis was continued on sections additionally labeled for KP. The TH-IR neurons showed a lower level of co-labeling for KP in lactating mice compared to OVX+E2 mice (16.1 ± 5% vs. 57.8 ± 4.3%). Removing the pups for 24 h did not alter significantly the KP production in TH-IR neurons (17.3 ± 4.6%). The mean number of GnRH-IR varicosities on preoptic and arcuate TH cells did not differ in the three animal models investigated. This study shows evidence that GnRH neurons provide direct synaptic inputs to POA and Arc dopaminergic neurons. The scale of anatomical connectivity with these target cells was unaltered during lactation indicating a maintained GnRH input, inspite of the altered hormonal condition.

Highlights

  • The gonadotropin-releasing hormone (GnRH) neurons are thought to form the final common pathway for central regulation of fertility by receiving input from phenotypically diverse neurons of several brain regions, and projecting to the median eminence, where their peptide hormone is released to reach the adenohypophysis

  • The inhibitory signal transmission is predominantly activated via the shortloop feedback effect of prolactin itself, but neuronal afferents may contribute to the regulation of dopaminergic neurons [6]

  • The neuronal inputs can be supplementary in function to keep prolactin levels low, but may exert opposite effects to facilitate prolactin secretion at late pregnancy and/or during lactation

Read more

Summary

Introduction

The gonadotropin-releasing hormone (GnRH) neurons are thought to form the final common pathway for central regulation of fertility by receiving input from phenotypically diverse neurons of several brain regions, and projecting to the median eminence, where their peptide hormone is released to reach the adenohypophysis. It is well-known, that cellular elements of the neuronal circuit regulating GnRH secretion receive indirect information about the secretory activity of GnRH neurons via hormonal feedback from the periphery; in contrast, it is less understood whether efferents of GnRH neurons can directly influence the hypothalamic neuronal circuitry that controls fertility.

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call