Evidence map›Paper›PMID 37610243›Full record

ArticleEndocrinology2023

Effect of Fetal Pituitary-Testes Suppression on Brain Sexual Differentiation and Reproductive Function in Male Sheep.

Rebecka Amodei, Sonnet S Jonker, Mary Smallman, William Whitler, Charles T Estill, Charles E Roselli

Open access · greenAbstract read
In one paragraph

Article in Endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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 at 2 institutions in 1 country.

Rebecka AmodeiDepartment of Chemical Physiology and Biochemistry, Oregon Health & Science University, Portland, OR 97239-3098, USA.
Sonnet S JonkerCenter for Developmental Health, Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR 97239-3098, USA.
Mary SmallmanDepartment of Animal and Rangeland Sciences, Oregon State University, Corvallis, OR 97331-4501, USA.
William WhitlerCollege of Veterinary Medicine, Oregon State University, Corvallis, OR 97331-4501, USA.
Charles T EstillDepartment of Animal and Rangeland Sciences, Oregon State University, Corvallis, OR 97331-4501, USA.
Charles E RoselliDepartment of Chemical Physiology and Biochemistry, Oregon Health & Science University, Portland, OR 97239-3098, USA.ORCID 0000-0002-9772-6101
Oregon Health & Science University · USOregon State University · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
A Ram Model of Neuroendocrine FunctionR01OD011047 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI ROSELLI, CHARLES E. · 2012 to 2023
$4.8M
NIH HHS P51 OD011092NIH HHS R01 OD011047
6 · The paper itself

Abstract

We previously demonstrated that treating fetal lambs on gestational day 62 with the long-acting gonadotrophin-releasing hormone (GnRH) antagonist degarelix (DG) suppresses pituitary-testicular function during midgestation. The objective of this study was to investigate whether impaired gonadotrophic drive during this fetal period has enduring effects on sexual differentiation and reproductive function in adult male sheep. We assessed the effects of prenatal administration of DG, with or without testosterone (T) replacement, on various sexually dimorphic behavioral traits in adult rams, including sexual partner preferences, as well as neuroendocrine responsiveness and testicular function. Our findings revealed that DG treatment had no effect on genital differentiation or somatic growth. There were some indications that DG treatment suppressed juvenile play behavior and adult sexual motivation; however, male-typical sexual differentiation of reproductive behavior, sexual partner preference, and gonadotropin feedback remained unaffected and appeared to be fully masculinized and defeminized. DG-treated rams showed an increased LH response to GnRH stimulation and a decreased T response to human chorionic gonadotropin stimulation, suggesting impaired Leydig cell function and reduced T feedback. Both effects were reversed by cotreatment with T propionate. DG treatment also suppressed the expression of CYP17 messenger RNA, a key enzyme for T biosynthesis. Despite the mild hypogonadism induced by DG treatment, ejaculate volume, sperm motility, and sperm morphology were not affected. In summary, these results suggest that blocking GnRH during midgestation does not have enduring effects on brain sexual differentiation but does negatively affect the testes' capacity to synthesize T.

Indexed as

Pituitary DiseasesTestisAdultAnimalsBrainFemaleGonadotropin-Releasing HormoneHumansMalePregnancySemenSex DifferentiationSheepSheep, DomesticSperm MotilityGonadotropin-Releasing HormoneGnRHLH secretionsexual behaviorsexual differentiationsexually dimorphic nucleussexual partner preference

Identifiers

PMID37610243
PMCPMC10484288
OpenAlexW4386084654

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.