Evidence map›Paper›PMID 25392497›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Sexual differentiation of the brain requires perinatal kisspeptin-GnRH neuron signaling.

Jenny Clarkson, Ellen R Busby, Milen Kirilov, Günther Schütz, Nancy M Sherwood, Allan E Herbison

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

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  9. Maternal organophosphate flame retardant exposure alters the developing mesencephalic dopamine system in fetal rat.Toxicological sciences : an official journal of the Society of Toxicology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jenny ClarksonCentre for Neuroendocrinology and Department of Physiology, School of Medical Sciences, University of Otago, Dunedin 9054, New Zealand.
Ellen R BusbyDepartment of Biology, University of Victoria, Victoria, British Columbia, V8P 5C2 Canada, and.
Milen KirilovMolecular Biology of the Cell, German Cancer Research Centre, 69120 Heidelberg, Germany.
Günther SchützMolecular Biology of the Cell, German Cancer Research Centre, 69120 Heidelberg, Germany.
Nancy M SherwoodDepartment of Biology, University of Victoria, Victoria, British Columbia, V8P 5C2 Canada, and.
Allan E HerbisonCentre for Neuroendocrinology and Department of Physiology, School of Medical Sciences, University of Otago, Dunedin 9054, New Zealand, allan.herbison@otago.ac.nz.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sex differences in brain function underlie robust differences between males and females in both normal and disease states. Although alternative mechanisms exist, sexual differentiation of the male mammalian brain is initiated predominantly by testosterone secreted by the testes during the perinatal period. Despite considerable advances in understanding how testosterone and its metabolite estradiol sexually differentiate the brain, little is known about the mechanism that generates the male-specific perinatal testosterone surge. In mice, we show that a male-specific activation of GnRH neurons occurs 0-2 h following birth and that this correlates with the male-specific surge of testosterone occurring up to 5 h after birth. The necessity of GnRH signaling for the sexually differentiating effects of the perinatal testosterone surge was demonstrated by the persistence of female-like brain characteristics in adult male, GnRH receptor knock-out mice. Kisspeptin neurons have recently been identified to be potent, direct activators of GnRH neurons. We demonstrate that a population of kisspeptin neurons appears in the preoptic area of only the male between E19 and P1. The importance of kisspeptin inputs to GnRH neurons for the process of sexual differentiation was demonstrated by the lack of a normal neonatal testosterone surge, and disordered brain sexual differentiation of male mice in which the kisspeptin receptor was deleted selectively from GnRH neurons. These observations demonstrate the necessity of perinatal GnRH signaling for driving brain sexual differentiation and indicate that kisspeptin inputs to GnRH neurons are essential for this process to occur.

Indexed as

Signal TransductionAnimalsAnimals, NewbornFemaleGonadotropin-Releasing HormoneMaleMiceMice, KnockoutNeuronsPregnancyPreoptic AreaReceptors, G-Protein-CoupledReceptors, Kisspeptin-1Receptors, LHRHSex CharacteristicsSex DifferentiationGonadotropin-Releasing HormoneKiss1r protein, mouseReceptors, G-Protein-CoupledReceptors, Kisspeptin-1Receptors, LHRHTestosteroneTyrosine 3-MonooxygenaseVasopressinsGnRHGPR54kisspeptinsexual differentiationtestosterone

Identifiers

PMID25392497
PMCPMC6608447

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.