Cited by 81Hypothalamic control of reproductive hormonesNeuroendocrine regulation and behaviorRegulation of Appetite and Obesity

Definition of Brainstem Afferents to Gonadotropin-Releasing Hormone Neurons in the Mouse Using Conditional Viral Tract Tracing

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Campbell, Rebecca E., Herbison, Allan E.·2007·Endocrinology

Abstract

Brainstem monoamines have long been considered to play a role in regulating the activity of GnRH neurons, although their neuroanatomical relationship with these cells has remained unclear. Using a Cre-dependent pseudorabies virus (Ba2001) technique that permits retrograde tracing selectively from GnRH neurons in the mouse, we have examined the organization of brainstem inputs to rostral preoptic area (rPOA) GnRH neurons. Two days after injection of Ba2001 into the rPOA of adult female GnRH-Cre transgenic mice, five to nine GnRH neurons located immediately adjacent to the injection site were found to express green fluorescent protein (GFP), the marker of virus infection, with no GFP expression anywhere else in the brain. In mice killed 24 h later (3 d after injection), GFP-expressing cells were identified (in order of density) in the raphe nuclei, periaqueductal grey, locus coeruleus, nucleus tractus solitarius, and area postrema. This time course is compatible with these neurons representing primary afferent inputs to the GnRH neurons. Four and 6 d after Ba2001 injection, GFP-expressing cells were found in additional brain regions. Dual-label immunofluorescence experiments in 3-d postinjection mice demonstrated that 100% of GFP-expressing neurons in the raphe were positive for tryptophan hydroxylase, whereas 100% and approximately 50% of GFP neurons in the locus coeruleus and nucleus tractus solitarius, respectively, expressed tyrosine hydroxylase. These observations demonstrate that rPOA GnRH neurons receive direct projections from brainstem A2 and A6 noradrenergic neurons and that, surprisingly, the largest afferent input from the brainstem originates from raphe serotonin neurons in the mouse.

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  • Inputs from the A1, A2, and locus coeruleus (LC)-NA cell groups to GnRH neuron cell bodies have been demonstrated in various species.

    “Research over the last few decades has focused attention on the GnRH neurons and resulted in the demonstration of inputs from the A1, A2, and locus coeruleus (LC)-NA cell groups to the GnRH neuron cell bodies in various species20–23.”

    From Brainstem noradrenergic modulation of the kisspeptin neuron GnRH pulse generator in mice (2025) · cites this paper as [23]

    The Discussion (page not provided) reports direct inputs from A2 and A6 (locus coeruleus) neurons to mouse GnRH neurons, and describes A1/A2 inputs in rats and A1/A6 inputs in sheep. But the rat and sheep evidence places those inputs in the vicinity of GnRH cell bodies, not necessarily onto the cell bodies; the study found no direct A1 input in mice. (LLM, conf=0.87)

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Authors
Campbell, R. E., & Herbison, A. E.
Affiliations
University of Otago (NZ)
Venue
Endocrinology
Published
2007-12-01
Volume
148
Issue
12
Pages
5884-5890
ISSN
  • 0013-7227 (ISSN-L)
  • 1945-7170
OpenAlex
W2065907632
Cited by
81
References
3
Citations by year
2026: 1 · 2025: 2 · 2024: 3 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 1 · 2019: 3 · 2018: 3 · 2017: 2 · 2016: 4 · 2015: 3 · 2014: 8 · 2013: 3 · 2012: 9
FWCI
6.63
Type
journal article
Language
en
Open access
Locations
  • Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
Wellcome Trust
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
  • Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
Keywords
GnRH neurons, retrograde tracing, noradrenergic neurons, tryptophan hydroxylase, locus coeruleus, nucleus tractus solitarius, periaqueductal gray, area postrema, monoamines
MeSH terms
Animals, Brain Stem, Female, Immunohistochemistry, Gonadotropin-Releasing Hormone, Mice, Transgenic, Models, Biological, Neurons, Neurons, Afferent, Preoptic Area, Herpesvirus 1, Suid, Time Factors, Microscopy, Confocal, Green Fluorescent Proteins, Mice

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