Evidence map›Paper›PMID 39117904›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2024

Identification of a stress-responsive subregion of the basolateral amygdala in male rats.

Robert J Aukema, Gavin N Petrie, Avi K Matarasso, Samantha L Baglot, Leonardo A Molina, Tamás Füzesi, Sandra Kadhim, Andrei S Nastase, Itzel Rodriguez Reyes, Jaideep S Bains and 3 more

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. 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

13 authors.

Robert J AukemaHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.ORCID http://orcid.org/0000-0003-3490-3390
Gavin N PetrieHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Avi K MatarassoBioengineering, University of Washington, Seattle, WA, 98195, USA.
Samantha L BaglotHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.ORCID http://orcid.org/0000-0001-8898-2122
Leonardo A MolinaHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Tamás FüzesiHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.ORCID http://orcid.org/0000-0001-9261-9828
Sandra KadhimHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Andrei S NastaseHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Itzel Rodriguez ReyesAnesthesiology and Pain Medicine, University of Washington, Seattle, WA, 98195, USA.
Jaideep S BainsHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Maria MorenaHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.ORCID http://orcid.org/0000-0001-6590-8130
Michael R BruchasBioengineering, University of Washington, Seattle, WA, 98195, USA.ORCID http://orcid.org/0000-0003-4713-7816
Matthew N HillHotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada. mnhill@ucalgary.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The basolateral amygdala (BLA) is reliably activated by psychological stress and hyperactive in conditions of pathological stress or trauma; however, subsets of BLA neurons are also readily activated by rewarding stimuli and can suppress fear and avoidance behaviours. The BLA is highly heterogeneous anatomically, exhibiting continuous molecular and connectivity gradients throughout the entire structure. A critical gap remains in understanding the anatomical specificity of amygdala subregions, circuits, and cell types explicitly activated by acute stress and how they are dynamically activated throughout stimulus exposure. Using a combination of topographical mapping for the activity-responsive protein FOS and fiber photometry to measure calcium transients in real-time, we sought to characterize the spatial and temporal patterns of BLA activation in response to a range of novel stressors (shock, swim, restraint, predator odour) and non-aversive, but novel stimuli (crackers, citral odour). We report four main findings: (1) the BLA exhibits clear spatial activation gradients in response to novel stimuli throughout the medial-lateral and dorsal-ventral axes, with aversive stimuli strongly biasing activation towards medial aspects of the BLA; (2) novel stimuli elicit distinct temporal activation patterns, with stressful stimuli exhibiting particularly enhanced or prolonged temporal activation patterns; (3) changes in BLA activity are associated with changes in behavioural state; and (4) norepinephrine enhances stress-induced activation of BLA neurons via the ß-noradrenergic receptor. Moving forward, it will be imperative to combine our understanding of activation gradients with molecular and circuit-specificity.

Indexed as

Basolateral Nuclear ComplexStress, PsychologicalAnimalsMaleNeuronsOdorantsProto-Oncogene Proteins c-fosRatsRats, Sprague-DawleyProto-Oncogene Proteins c-fos

Identifiers

PMID39117904
PMCPMC11480132

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.