Evidence map›Paper›PMID 15843602›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Gonadal steroid attenuation of developing hamster facial motoneuron loss by axotomy: equal efficacy of testosterone, dihydrotestosterone, and 17-beta estradiol.

Christopher B Huppenbauer, Lisa Tanzer, Lydia L DonCarlos, Kathryn J Jones

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.8field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
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  4. Biological Sex Disparities in Alzheimer's Disease.Current topics in behavioral neurosciences · 2025
    Review
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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 2 countries.

Christopher B HuppenbauerDepartment of Cell Biology, Neurobiology, and Anatomy, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois 60153, USA.
Lisa Tanzer
Lydia L DonCarlos
Kathryn J Jones
Loyola University Chicago · US

Funding

Androgen Receptor Expression in Developing Rat ForebrainR01MH062588 · NIMH · LOYOLA UNIVERSITY CHICAGO · PI DONCARLOS, LYDIA L · 2001 to 2005
$1.4M
STEROID HORMONES AND NEURONAL REGENERATIONR01NS028238 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI JONES, KATHRYN JANE · 1990 to 2001
$668k
ONTOGENY OF ESTROGEN TARGET NEURONS IN THE FOREBRAINR29MH048794 · NIMH · LOYOLA UNIVERSITY CHICAGO · PI DONCARLOS, LYDIA L · 1992 to 1996
–
NIMH NIH HHS MH48794NIMH NIH HHS MH62588NIMH NIH HHS R01 MH062588NINDS NIH HHS NS-28238NINDS NIH HHS R01 NS028238
6 · The paper itself

Abstract

In the hamster facial nerve injury paradigm, we have established that androgens enhance both functional recovery from facial nerve paralysis and the rate of regeneration in the adult, through intrinsic effects on the nerve cell body response to injury and via an androgen receptor (AR)-mediated mechanism. Whether these therapeutic effects of gonadal steroids encompass neuroprotection from axotomy-induced cell death is the focus of the present study. Virtually 100% of adult hamster facial motoneurons (FMNs) survive axotomy at the stylomastoid foramen (SMF), whereas, before postnatal day 15 (P15), developing FMNs undergo substantial axotomy-induced cell death. The first part of the present study focuses on determining when ARs are first expressed in developing hamster FMNs. Using AR immunocytochemistry, it was found that males express ARs by P2 and females by P4, which is the earliest demonstration of AR expression in mammalian motoneurons reported thus far in the literature. The second half examines the neuroprotective effects of testosterone propionate, 17-beta estradiol, and dihydrotestosterone on FMNs of P7 hamsters after facial nerve transection at the SMF. The results demonstrate that androgens and estrogens are equally able to rescue approximately 20% of FMNs from axotomy-induced cell death, with the effects permanent. This study is the first to investigate the effects of both androgens and estrogens on axotomy-induced cell death in one system and, with our previously published work, to validate the hamster FMN injury paradigm as a model of choice in the investigation of both neurotherapeutic and neuroprotective actions of gonadal steroids.

Indexed as

Age FactorsAnimalsAnimals, NewbornAxotomyBrain StemCell CountCell DeathCricetinaeDihydrotestosteroneDisease Models, AnimalDose-Response Relationship, DrugEstradiolFacial Nerve InjuriesFemaleFunctional LateralityGene Expression Regulation, DevelopmentalDihydrotestosteroneEstradiolGonadal Steroid HormonesReceptors, AndrogenTestosterone

Identifiers

PMID15843602
PMCPMC6724945
OpenAlexW2005333476

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.