Evidence map›Paper›PMID 23046854›Full record

ArticlePharmacology, biochemistry, and behavior2013

RU486 blocks effects of allopregnanolone on the response to restraint stress.

Lynda Uphouse, Sarah Adams, Chandra Suma Johnson Miryala, James Hassell, Cindy Hiegel

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 12 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

5 authors at 1 institution in 1 country.

Lynda UphouseDepartment of Biology, Texas Woman's University, United States. LUphouse@mail.twu.edu
Sarah Adams
Chandra Suma Johnson Miryala
James Hassell
Cindy Hiegel
Texas Woman's University · US

Funding

REDUCED LORDOSIS BEHAVIOR AFTER INTRACEREBRAL 8-OH-DPATR01HD028419 · NICHD · TEXAS WOMAN'S UNIVERSITY · PI UPHOUSE, LYNDA L · 1991 to 2011
$2.0M
NICHD NIH HHS R01 HD028419PHS HHS NIHHD28419
6 · The paper itself

Abstract

These experiments were designed to provide information about the potential involvement of progesterone receptors in the ability of allopregnanolone (3α-hydroxy-5α-pregnan-20-one) to reduce the lordosis-inhibiting effects of restraint stress. Ovariectomized Fischer rats were hormonally primed with 10 μg estradiol benzoate and 4 mg/kg allopregnanolone or vehicle. One hour before allopregnanolone, rats were injected with the progesterone receptor antagonist, RU486 (11β-(4-dimethylamino)phenyl-17β-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one), or vehicle. Four hours after allopregnanolone or vehicle, sexual behavior was examined before and after a 5-min restraint stress. Lordosis behavior of rats primed only with estradiol benzoate declined after the 5 min of restraint while allopregnanolone prevented this decline. RU486 attenuated the ability of allopregnanolone to prevent the restraint-induced decline in lordosis behavior. These findings are consistent with earlier suggestions that progesterone receptors are involved in allopregnanolone's ability to reduce the effects of restraint stress.

Indexed as

AnimalsDrug InteractionsFemaleMaleMifepristonePosturePregnanoloneRatsRats, Inbred F344Receptors, ProgesteroneSexual Behavior, AnimalStress, PsychologicalMifepristonePregnanoloneReceptors, Progesterone

Identifiers

PMID23046854
PMCPMC3545068
OpenAlexW1991849828

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.