Evidence map›Paper›PMID 33647571›Full record

ArticlePsychoneuroendocrinology2021

Chronic psychosocial stress and experimental pubertal delay affect socioemotional behavior and amygdala functional connectivity in adolescent female rhesus macaques.

Melanie Pincus, Jodi R Godfrey, Eric Feczko, Eric Earl, Oscar Miranda-Dominguez, Damien Fair, Mark E Wilson, Mar M Sanchez, Clare Kelly

Open access · hybridAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2021. 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
1.1field-weighted citation impact, top 29% 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, 12 citations in OpenAlex.

  1. Review
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  4. 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

9 authors at 6 institutions in 2 countries.

Melanie PincusDivision of Developmental and Cognitive Neuroscience, Yerkes National Primate Research Center, Emory University, Atlanta, GA, USA.
Jodi R GodfreyDivision of Developmental and Cognitive Neuroscience, Yerkes National Primate Research Center, Emory University, Atlanta, GA, USA.
Eric FeczkoMasonic Institute for the Developing Brain (MIDB), University of Minnesota, Minneapolis, MN, USA; Institute of Child Development, College of Education and Human Development, University of Minnesota, Minneapolis, MN, USA; Department of Pediatrics, University of Minnesota Medical School, University of Minnesota, Minneapolis, MN, USA.
Eric EarlDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, USA.
Oscar Miranda-DominguezMasonic Institute for the Developing Brain (MIDB), University of Minnesota, Minneapolis, MN, USA; Institute of Child Development, College of Education and Human Development, University of Minnesota, Minneapolis, MN, USA; Department of Pediatrics, University of Minnesota Medical School, University of Minnesota, Minneapolis, MN, USA.
Damien FairMasonic Institute for the Developing Brain (MIDB), University of Minnesota, Minneapolis, MN, USA; Institute of Child Development, College of Education and Human Development, University of Minnesota, Minneapolis, MN, USA; Department of Pediatrics, University of Minnesota Medical School, University of Minnesota, Minneapolis, MN, USA.
Mark E WilsonDivision of Developmental and Cognitive Neuroscience, Yerkes National Primate Research Center, Emory University, Atlanta, GA, USA; Department of Psychiatry & Behavioral Sciences, Emory University, USA.
Mar M SanchezDivision of Developmental and Cognitive Neuroscience, Yerkes National Primate Research Center, Emory University, Atlanta, GA, USA.
Clare KellySchool of Psychology, Trinity College Dublin, Dublin, Ireland; Department of Psychiatry at the School of Medicine, Trinity College Dublin, Dublin, Ireland; Trinity College Institute of Neuroscience, Trinity College, Dublin, Ireland.
Emory University · USMidwest Orthopaedic Research Foundation · USMinnesota Department of Education · USOregon Health & Science University · USTrinity College Dublin · IEUniversity of Minnesota Medical Center · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Neurobiology of increased vulnerability to social stressors during adolescenceR01MH079100 · NIMH · EMORY UNIVERSITY · PI WILSON, MARK E · 2008 to 2012
$3.6M
Stress and Pubertal Timing Affect Amygdala Functional Circuitry in FemalesR03HD082534 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KELLY, ANNE MARIE CLARE · 2015 to 2016
$188k
NICHD NIH HHS R03 HD082534NIH HHS P51 OD011132NIMH NIH HHS R01 MH079100
6 · The paper itself

Abstract

In females, pubertal onset appears to signal the opening of a window of increased vulnerability to the effects of stress on neurobehavioral development. What is the impact of pubertal timing on this process? We assessed the effects of pubertal timing and stress on behavior and amygdala functional connectivity (FC) in adolescent female macaques, whose social hierarchy provides an ethologically valid model of chronic psychosocial stress. Monkeys experienced puberty spontaneously (n = 34) or pubertal delay via Lupron treatment from age 16-33 months (n = 36). We examined the effects of stress (continuous dimension spanning dominant/low-stress to subordinate/high-stress) and experimental pubertal delay (Lupron-treated vs. Control) on socioemotional behavior and FC at 43-46 months, after all animals had begun puberty. Regardless of treatment, subordinate monkeys were more submissive and less affiliative, and exhibited weaker FC between amygdala and dorsolateral prefrontal cortex and stronger FC between amygdala and temporal pole. Regardless of social rank, Lupron-treated monkeys were also more submissive and less affiliative but were less anxious and exhibited less displacement behavior in a "Human Intruder" task than untreated monkeys; they exhibited stronger FC between amygdala and orbitofrontal cortex. No interactions between rank and Lupron treatment were observed. These similar behavioral outcomes may reflect the common factor of delayed puberty - whether this is stress-related (untreated subordinate animals) or pharmacologically-induced (treated animals). In the brain, however, delayed puberty and subordination stress had separable effects, suggesting that the overlapping socioemotional outcomes may be mediated by distinct neuroplastic mechanisms. To gain further insights, additional longitudinal studies are required.

Indexed as

Puberty, DelayedStress, PsychologicalAmygdalaAnimalsEmotionsFemaleLeuprolideMacaca mulattaSocial BehaviorLeuprolideAdolescenceAmygdalaDevelopmentFunctional connectivityNonhuman primatesPubertySocioemotional behaviorStress

Identifiers

PMID33647571
PMCPMC11578542
OpenAlexW3129335568

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.