Evidence map›Paper›PMID 24650589›Full record

ArticlePharmacology, biochemistry, and behavior2014

Female mice with deletion of Type One 5α-reductase have reduced reproductive responding during proestrus and after hormone-priming.

Carolyn J Koonce, Cheryl A Frye

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Carolyn J KoonceDepartment of Psychology, University at Albany-SUNY, Albany, NY, United States; Institute of Arctic Biology, University of Alaska-Fairbanks, Fairbanks, AK, United States; IDeA Network of Biomedical Excellence (INBRE), University of Alaska-Fairbanks, Fairbanks, AK, United States.
Cheryl A FryeDepartment of Psychology, University at Albany-SUNY, Albany, NY, United States; Department of Biological Sciences, University at Albany-SUNY, Albany, NY, United States; The Centers for Neuroscience and Life Sciences Research, University at Albany-SUNY, Albany, NY, United States; Department of Chemistry & Biochemistry, University of Alaska-Fairbanks, Fairbanks, AK, United States; Institute of Arctic Biology, University of Alaska-Fairbanks, Fairbanks, AK, United States; IDeA Network of Biomedical Excellence (INBRE), University of Alaska-Fairbanks, Fairbanks, AK, United States. Electronic address: cafrye@alaska.edu.
University at Albany, State University of New York · USUniversity of Alaska Fairbanks · US

Funding

The Administrative CoreP20GM103395 · NIGMS · UNIVERSITY OF ALASKA FAIRBANKS · PI BRIAN M BARNES · 2012 to 2026
$66.1M
Progestogens' non-classical effects and mechanisms for social & mood processesR01MH067698 · NIMH · UNIVERSITY OF ALASKA FAIRBANKS · PI DREW, KELLY L · 2004 to 2013
$2.4M
Progestins' non-genomic actions for socio-sexual behaviorR56MH067698 · NIMH · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI FRYE, CHERYL ANNE · 2009 to 2009
$379k
NIGMS NIH HHS P20 GM103395NIGMS NIH HHS P20GM103395NIMH NIH HHS MH-06769801NIMH NIH HHS R01 MH067698NIMH NIH HHS R56 MH067698PHS HHS RMH067698B
6 · The paper itself

Abstract

The capacity to form progesterone (P₄)'s 5α-reduced metabolite, 5α-pregnan-3α-ol-20-one (3α,5α-THP; a.k.a. allopregnanolone), in the brain may be related to facilitation of lordosis among estrogen-primed (E₂) mice. We investigated this idea further by comparing effects of endogenous and exogenous progestogens in mice that are deficient in the Type One 5α-reductase enzyme (5α-reductase knockout mice; 5α-RKO), and their wildtype counterparts for sexual behavior. Comparisons were made following administration of progestogens that are expected to increase 3α,5α-THP or not. Sexual receptivity of 5α-RKO mice and their wildtype counterparts was examined when mice were naturally-cycling (Experiment 1); ovariectomized (OVX), E₂-primed (10 μg, subcutaneous; SC) and administered P₄ (0, 125, 250, or 500 μg SC; Experiment 2); and OVX, E₂-primed and administered P₄, medroxyprogesterone acetate (MPA, 4 mg/kg, SC, which does not convert to 3α,5α-THP) or 3α,5α-THP (4 mg/kg, SC; Experiment 3). The percentage of mounts that elicited lordosis (lordosis quotient) or aggression/rejection behavior (aggression quotient), as well as the quality of lordosis (lordosis rating), was scored. Wildtype, but not 5α-RKO, mice in behavioral estrus demonstrated significantly greater lordosis quotients and lordosis ratings, but similar aggression quotients, compared to their diestrous counterparts. Among OVX and E₂-primed mice, P₄ facilitated lordosis of wildtype, but not 5α-RKO, mice. MPA neither facilitated lordosis of wildtype, nor 5α-RKO mice. 3α,5α-THP administered to wildtype or 5α-RKO mice increased lordosis quotients and lordosis ratings and decreased aggression quotients. 3α,5α-THP levels in the midbrain, one brain region important for sexual behavior, were increased during behavioral estrus, with P4 administered to WT, but not 5α-RKO mice, and 3α,5α-THP administered to WT and 5α-RKO mice. MPA did not increase 3α,5α-THP. Thus, deletion of Type One 5α-reductase among female mice may attenuate reproductive responding during the estrous cycle and after hormone-priming.

Indexed as

3-Oxo-5-alpha-Steroid 4-DehydrogenaseAnimalsCholestenone 5 alpha-ReductaseFemaleMaleMembrane ProteinsMiceMice, KnockoutProestrusProgesteroneReproductionSexual Behavior, Animal3-Oxo-5-alpha-Steroid 4-DehydrogenaseCholestenone 5 alpha-ReductaseMembrane ProteinsProgesteroneSrd5a1 protein, mouseAllopregnanoloneLordosisMedroxyprogesterone acetateMidbrainSexual behavior

Identifiers

PMID24650589
PMCPMC4098936
OpenAlexW2043752769

What OpenQuestion holds

Textmetadata
LicenceTDM
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.