Evidence map›Paper›PMID 39299806›Full record

ArticleeNeuro2024

Examining Brain Activity Responses during Rat Ultrasonic Vocalization Playback: Insights from a Novel fMRI Translational Paradigm.

Lauren E Granata, Arnold Chang, Habiba Shaheed, Anjali Shinde, Praveen Kulkarni, Ajay Satpute, Heather C Brenhouse, Jennifer A Honeycutt

Abstract read
In one paragraph

Article in eNeuro, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Lauren E GranataDevelopmental Neuropsychobiology Laboratory, Department of Psychology, Northeastern University, Boston, Massachusetts 02115.ORCID https://orcid.org/0000-0002-3497-7296
Arnold ChangCenter for Translational Neuroimaging, Department of Psychology, Northeastern University, Boston, Massachusetts 02115.
Habiba ShaheedDevelopmental Neuropsychobiology Laboratory, Department of Psychology, Northeastern University, Boston, Massachusetts 02115.
Anjali ShindeCenter for Translational Neuroimaging, Department of Psychology, Northeastern University, Boston, Massachusetts 02115.
Praveen KulkarniCenter for Translational Neuroimaging, Department of Psychology, Northeastern University, Boston, Massachusetts 02115.
Ajay SatputeAffective and Brain Sciences Lab, Department of Psychology, Northeastern University, Boston, Massachusetts 02115.ORCID https://orcid.org/0000-0003-0227-0816
Heather C BrenhouseDevelopmental Neuropsychobiology Laboratory, Department of Psychology, Northeastern University, Boston, Massachusetts 02115.ORCID https://orcid.org/0000-0001-7591-4964
Jennifer A HoneycuttDevelopmental Neuropsychobiology Laboratory, Department of Psychology, Northeastern University, Boston, Massachusetts 02115 jhoneycu@bowdoin.edu.ORCID https://orcid.org/0000-0002-4879-0203

Funding

The Maine Biomedical Research Network (INBRE)P20GM103423 · NIGMS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI JAMES A COFFMAN · 2012 to 2026
$60.0M
NIGMS NIH HHS P20 GM103423
6 · The paper itself

Abstract

Despite decades of preclinical investigation, there remains limited understanding of the etiology and biological underpinnings of anxiety disorders. Sensitivity to potential threat is characteristic of anxiety-like behavior in humans and rodents, but traditional rodent behavioral tasks aimed to assess threat responsiveness lack translational value, especially with regard to emotionally valenced stimuli. Therefore, development of novel preclinical approaches to serve as analogues to patient assessments is needed. In humans, the fearful face task is widely used to test responsiveness to socially communicated threat signals. In rats, ultrasonic vocalizations (USVs) are analogous social cues associated with positive or negative affective states that can elicit behavioral changes in the receiver. It is therefore likely that when rats hear aversive alarm call USVs (22 kHz), they evoke translatable changes in brain activity comparable with the fearful face task. We used functional magnetic resonance imaging in male and female rats to assess changes in BOLD activity induced by exposure to aversive 22 kHz alarm calls emitted in response to threatening stimuli, prosocial (55 kHz) USVs emitted in response to appetitive stimuli, or a computer-generated 22 kHz tone. Results show patterns of regional activation that are specific to each USV stimulus. Notably, limbic regions clinically relevant to psychiatric disorders (e.g., amygdala, bed nucleus of the stria terminalis) are preferentially activated by either aversive 22 kHz or appetitive 55 kHz USVs. These results support the use of USV playback as a promising translational tool to investigate affective processing under conditions of distal threat in preclinical rat models.

Indexed as

BrainMagnetic Resonance ImagingVocalization, AnimalAnimalsFearFemaleMaleRatsRats, Sprague-Dawleybasolateral amygdalabed nucleus of the stria terminalisnegative valence systemstask-based fMRItranslational neuroscienceultrasonic vocalization

Identifiers

PMID39299806
PMCPMC11451431

What OpenQuestion holds

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LicenceCC BY
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.