Evidence map›Paper›PMID 26691962›Full record

ArticleNeuroscience2016

Anabolic steroids alter the physiological activity of aggression circuits in the lateral anterior hypothalamus.

T R Morrison, R W Sikes, R H Melloni

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Contemporary Pharmacotherapeutics and the Management of Aggressive Behavior in an Adolescent Animal Model of Maladaptive Aggression.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2020
    Article
  2. Review
  3. Review
  4. Article
  5. 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

3 authors at 1 institution in 1 country.

T R MorrisonBehavioral Neuroscience Program, Department of Psychology, Northeastern University, Boston, MA 02115, United States.
R W SikesDepartment of Physical Therapy, Rehabilitation, and Movement Sciences, Northeastern University, Boston, MA 02115, United States.
R H MelloniBehavioral Neuroscience Program, Department of Psychology, Northeastern University, Boston, MA 02115, United States. Electronic address: r.melloni@neu.edu.
Northeastern University · US

Funding

ADOLESCENT ANABOLIC STEROIDS, VASOPRESSIN AND AGGRESSIONR01DA010547 · NIDA · NORTHEASTERN UNIVERSITY · PI MELLONI, RICHARD H. · 2003 to 2015
$2.8M
ADOLESCENT ANABOLIC STEROIDS, VASOPRESSION, &AGGRESSIONR29DA010547 · NIDA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MELLONI, RICHARD H. · 1996 to 2002
$137k
NIDA NIH HHS R01 DA010547NIDA NIH HHS R01 DA10547NIDA NIH HHS R29 DA010547
6 · The paper itself

Abstract

Syrian hamsters exposed to anabolic/androgenic steroids (AAS) during adolescence consistently show increased aggressive behavior across studies. Although the behavioral and anatomical profiles of AAS-induced alterations have been well characterized, there is a lack of data describing physiological changes that accompany these alterations. For instance, behavioral pharmacology and neuroanatomical studies show that AAS-induced changes in the vasopressin (AVP) neural system within the latero-anterior hypothalamus (LAH) interact with the serotonin (5HT) and dopamine (DA) systems to modulate aggression. To characterize the electrophysiological profile of the AAS aggression circuit, we recorded LAH neurons in adolescent male hamsters in vivo and microiontophoretically applied agonists and antagonists of aggressive behavior. The interspike interval (ISI) of neurons from AAS-treated animals correlated positively with aggressive behaviors, and adolescent AAS exposure altered parameters of activity in regular firing neurons while also changing the proportion of neuron types (i.e., bursting, regular, irregular). AAS-treated animals had more responsive neurons that were excited by AVP application, while cells from control animals showed the opposite effect and were predominantly inhibited by AVP. Both DA D2 antagonists and 5HT increased the firing frequency of AVP-responsive cells from AAS animals and dual application of AVP and D2 antagonists doubled the excitatory effect of AVP or D2 antagonist administration alone. These data suggest that multiple DA circuits in the LAH modulate AAS-induced aggressive responding. More broadly, these data show that multiple neurochemical interactions at the neurophysiological level are altered by adolescent AAS exposure.

Indexed as

Action PotentialsAggressionAnabolic AgentsAnimalsDopamine D2 Receptor AntagonistsHypothalamic Area, LateralHypothalamus, AnteriorMaleMesocricetusNeuronsReceptors, Dopamine D2SalicylamidesSerotoninSteroidsVasopressinsAnabolic AgentsDopamine D2 Receptor AntagonistseticloprideReceptors, Dopamine D2SalicylamidesSerotoninSteroidsVasopressinsaggressiondevelopmentdopaminehypothalamusserotoninvasopressin

Identifiers

PMID26691962
PMCPMC4720269
OpenAlexW2194750199

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.