Evidence map›Paper›PMID 33075809›Full record

ArticleEndocrinology2020

Androgen Suppresses In Vivo and In Vitro LH Pulse Secretion and Neural Kiss1 and Tac2 Gene Expression in Female Mice.

Lourdes A Esparza, Tomohiro Terasaka, Mark A Lawson, Alexander S Kauffman

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
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

20 citing papers in PubMed, 31 citations in OpenAlex.

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  14. Reproductive capacity after gender-affirming testosterone therapy.Human reproduction (Oxford, England) · 2023
    Article
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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

4 authors at 1 institution in 1 country.

Lourdes A EsparzaDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of California San Diego, La Jolla, California.
Tomohiro TerasakaDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of California San Diego, La Jolla, California.
Mark A LawsonDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of California San Diego, La Jolla, California.
Alexander S KauffmanDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of California San Diego, La Jolla, California.
University of California San Diego · US

Funding

The Role of FSH in Female InfertilityP50HD012303 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LAWSON, MARK ANDREW · 1985 to 2020
$7.5M
CRR LIGAND ASSAY AND ANALYSIS CORER24HD102061 · NICHD · UNIVERSITY OF VIRGINIA · PI HAISENLEDER, DANIEL J. · 2019 to 2023
$2.2M
Neuroendocrine regulation of puberty and reproductive developmentR01HD090161 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KAUFFMAN, ALEXANDER S · 2017 to 2021
$1.9M
Neuroendocrine Actions of Androgens in Female ReproductionR01HD082567 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MELLON, PAMELA L · 2015 to 2019
$1.6M
NICHD NIH HHS P50 HD012303NICHD NIH HHS R01 HD082567NICHD NIH HHS R01 HD090161NICHD NIH HHS R24 HD102061
6 · The paper itself

Abstract

Androgens can affect the reproductive axis of both sexes. In healthy women, as in men, elevated exogenous androgens decrease gonad function and lower gonadotropin levels; such circumstances occur with anabolic steroid abuse or in transgender men (genetic XX individuals) taking androgen supplements. The neuroendocrine mechanisms by which endogenous or exogenous androgens regulate gonadotropin release, including aspects of pulsatile luteinizing hormone (LH) secretion, remain unknown. Because animal models are valuable for interrogating neural and pituitary mechanisms, we studied effects of androgens in the normal male physiological range on in vivo LH secretion parameters in female mice and in vitro LH secretion patterns from isolated female pituitaries. We also assessed androgen effects on hypothalamic and gonadotrope gene expression in female mice, which may contribute to altered LH secretion profiles. We used a nonaromatizable androgen, dihydrotestosterone (DHT), to isolate effects occurring specifically via androgen receptor (AR) signaling. Compared with control females, DHT-treated females exhibited markedly reduced in vivo LH pulsatility, with decreases in pulse frequency, amplitude, peak, and basal LH levels. Correlating with reduced LH pulsatility, DHT-treated females also exhibited suppressed arcuate nucleus Kiss1 and Tac2 expression. Separate from these neural effects, we determined in vitro that the female pituitary is directly inhibited by AR signaling, resulting in lower basal LH levels and reduced LH secretory responses to gonadotropin-releasing hormone pulses, along with lower gonadotropin gene expression. Thus, in normal adult females, male levels of androgen acting via AR can strongly inhibit the reproductive axis at both the neural and pituitary levels.

Indexed as

AndrogensAnimalsDihydrotestosteroneFemaleGonadotropin-Releasing HormoneHypothalamusKisspeptinsLuteinizing HormoneMaleMiceNeuronsPituitary GlandProtein PrecursorsSignal TransductionTachykininsAndrogensDihydrotestosteroneGonadotropin-Releasing HormoneKiss1 protein, mouseKisspeptinsLuteinizing HormonepreprotachykininProtein PrecursorsTachykininsandrogenandrogen receptorDHTGnRHgonadotropeKiss1kisspeptinneurokinin BpituitaryTac2

Identifiers

PMID33075809
PMCPMC7671291
OpenAlexW3093395452

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.