Evidence map›Paper›PMID 27238893›Full record

ArticleNeuroscience2016

Anabolic-androgenic steroids decrease dendritic spine density in the nucleus accumbens of male rats.

Kathryn Wallin-Miller, Grace Li, Diana Kelishani, Ruth I Wood

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Neurosteroids and the mesocorticolimbic system.Neuroscience and biobehavioral reviews · 2023
    Review
  6. Review
  7. Perinatal activation of ERJournal of neurophysiology · 2021
    Article
  8. Review
  9. Sex Differences and the Effects of Estradiol on Striatal Function.Current opinion in behavioral sciences · 2018
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
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.

Kathryn Wallin-MillerNeuroscience Graduate Program, University of Southern California, Los Angeles, CA 90033, USA. Electronic address: kwallin@usc.edu.
Grace LiDepartment of Cell and Neurobiology, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA. Electronic address: lir@usc.edu.
Diana KelishaniDepartment of Cell and Neurobiology, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA; Department of Pharmaceutical Biosciences, Uppsala University, Sweden.
Ruth I WoodDepartment of Cell and Neurobiology, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA. Electronic address: riw@usc.edu.
University of Southern California · US

Funding

Anabolic-androgenic steroids promote risky decision makingR01DA029613 · NIDA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JAKOWEC, MICHAEL WALTER, WOOD, RUTH I. · 2011 to 2019
$2.9M
NIDA NIH HHS R01 DA029613
6 · The paper itself

Abstract

Recent studies have demonstrated that anabolic-androgenic steroids (AAS) modify cognitive processes such as decision making and behavioral flexibility. However, the neural mechanisms underlying these AAS-induced cognitive changes remain poorly understood. The mesocorticolimbic dopamine (DA) system, particularly the nucleus accumbens (Acb), is important for reward, motivated behavior, and higher cognitive processes such as decision making. Therefore, AAS-induced plasticity in the DA system is a potential structural substrate for the observed cognitive alterations. High doses of testosterone (the most commonly-used AAS) increase dendritic spine density in limbic regions including the amygdala and hippocampus. However, effects on Acb are unknown. This was the focus of the present study. Adolescent male Long-Evans rats were treated chronically for 8weeks with high-dose testosterone (7.5mg/kg in water with 13% cyclodextrin) or vehicle sc. Brains were stained by Golgi-Cox to analyze neuronal morphology in medium spiny neurons of the shell region of Acb (AcbSh). Eightweeks of testosterone treatment significantly decreased spine density in AcbSh compared to brains of vehicle-treated rats (F1,14=5.455, p<0.05). Testosterone did not significantly affect total spine number, dendritic length, or arborization measured by Sholl analysis. These results show that AAS alter neuronal morphology in AcbSh by decreasing spine density throughout the dendritic tree, and provides a potential mechanism for AAS to modify cognition and decision-making behavior.

Indexed as

Analysis of VarianceAndrogensAnimalsCell SizeDendritic SpinesDisease Models, AnimalMaleNucleus AccumbensRats, Long-EvansSubstance-Related DisordersTestosteroneAndrogensTestosteroneanabolic agentsdendritic spine densitymedium spiny neuronsnucleus accumbenstestosterone

Identifiers

PMID27238893
PMCPMC4927385
OpenAlexW2402597005

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.