Evidence map›Paper›PMID 34487822›Full record

ArticleNeuroscience2021

Role of Basolateral Amygdalar Somatostatin 2 Receptors in a Rat Model of Chronic Anxiety.

Denise L Gaskins, Andrew R Burke, Tammy J Sajdyk, William A Truitt, Amy D Dietrich, Anantha Shekhar

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

6 authors at 4 institutions in 1 country.

Denise L GaskinsStark Neurosciences Research Institute, Indiana University School of Medicine, 320 W. 15th Street, Indianapolis, IN 46202, USA; Graduate Program in Medical Neuroscience, Indiana University School of Medicine, 320 W. 15th Street, Indianapolis, IN 46202, USA.
Andrew R BurkeStark Neurosciences Research Institute, Indiana University School of Medicine, 320 W. 15th Street, Indianapolis, IN 46202, USA; Department of Anatomy Cellular Biology & Physiology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202, USA.
Tammy J SajdykDepartment of Psychiatry, Indiana University School of Medicine, 355 W. 16th Street, Indianapolis, IN 46202, USA; Indiana Clinical and Translational Sciences Institute, Indiana University School of Medicine, 410 W 10th St Suite 1000, Indianapolis, IN 46202, USA; Department of Pediatrics, Division of Hematology/Oncology, Indiana University School of Medicine, 705 Riley Hospital Drive, Indianapolis, IN 46202, USA.
William A TruittStark Neurosciences Research Institute, Indiana University School of Medicine, 320 W. 15th Street, Indianapolis, IN 46202, USA; Department of Anatomy Cellular Biology & Physiology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202, USA. Electronic address: btruitt@iupui.edu.
Amy D DietrichStark Neurosciences Research Institute, Indiana University School of Medicine, 320 W. 15th Street, Indianapolis, IN 46202, USA; Department of Anatomy Cellular Biology & Physiology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202, USA.
Anantha ShekharStark Neurosciences Research Institute, Indiana University School of Medicine, 320 W. 15th Street, Indianapolis, IN 46202, USA; Department of Psychiatry, Indiana University School of Medicine, 355 W. 16th Street, Indianapolis, IN 46202, USA; Indiana Clinical and Translational Sciences Institute, Indiana University School of Medicine, 410 W 10th St Suite 1000, Indianapolis, IN 46202, USA; Department of Psychiatry, University of Pittsburgh School of Medicine, 3550 Terrace Street, Suite 401, Pittsburgh, PA 15261, USA.
Indiana University – Purdue University Indianapolis · USIndiana Clinical and Translational Sciences Institute · USIndiana University School of MedicineRiley Hospital for Children · US

Funding

NEUROBIOLOGY OF PANIC AND ANXIETY DISORDERSR01MH052619 · NIMH · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SHEKHAR, ANANTHA · 1996 to 2016
$5.0M
Serotonin and CRF Pathways in Anxiety &HPA RegulationR01MH065702 · NIMH · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI LOWRY, CHRISTOPHER A, SHEKHAR, ANANTHA · 2003 to 2013
$2.8M
NEURAL REGULATION OF SOCIAL FAMILIARITY INDUCED ANXIOLYSIS ALZHEIMER S SupplementR01MH106568 · NIMH · INDIANA UNIVERSITY INDIANAPOLIS · PI TRUITT, WILLIAM ANTHONY · 2015 to 2019
$2.8M
Mechanisms of Serotonin Modulation of PanicR01MH122843 · NIMH · INDIANA UNIVERSITY INDIANAPOLIS · PI TRUITT, WILLIAM ANTHONY · 2020 to 2024
$2.6M
NIMH NIH HHS R01 MH052619NIMH NIH HHS R01 MH065702NIMH NIH HHS R01 MH106568NIMH NIH HHS R01 MH122843
6 · The paper itself

Abstract

Repeated exposure to stress has been implicated in inducing chronic anxiety states. Stress related increases in anxiety responses are likely mediated by activation of corticotropin-releasing factor receptors (CRFR) in the amygdala, particularly the basolateral amygdala (BLA). Within the BLA, acute injections of the CRFR agonist urocortin 1 (Ucn1) leads to acute anxiety, whereas repeated daily injections of subthreshold-doses of Ucn1 produces a long-lasting, persistent anxiety-like phenotype, a phenomenon referred to as Ucn1-priming. Relative gene expressions from the BLA of vehicle and Ucn1-primed rats were analyzed with quantitative RT-PCR using a predesigned panel of 82 neuroscience-related genes. Compared to vehicle-primed rats, only expression of the somatostatin receptor 2 gene (Sstr2) was significantly reduced in the BLA of Ucn1-primed rats. The contribution of Sstr2 on an anxiety phenotype was tested by injecting a Sstr2 antagonist into the BLA in un-primed rats. The Sstr2 antagonist increased anxiety-like behavior. Notably, pretreatment with Sstr2 agonist injected into the BLA blocked anxiety-inducing effects of acute Ucn1 BLA-injections and delayed anxiety expression during Ucn1-priming. However, concomitant Sstr2 agonist pretreatment during Ucn-1 priming did not prevent either the development of a chronic anxiety state or a reduction of BLA Sstr2 expression induced by priming. The data demonstrate that the persistent anxiety-like phenotype observed with Ucn1-priming in the BLA is associated with a selective reduction of Sstr2 gene expression. Although Sstr2 activation in the BLA blocks acute anxiogenic effects of stress and down-regulation of BLA Sstr2, it does not suppress the long-term consequences of prolonged exposure to stress-related challenges.

Indexed as

Basolateral Nuclear ComplexAnimalsAnxietyRatsRats, WistarReceptors, SomatostatinSomatostatinUrocortinsReceptors, SomatostatinSomatostatinSstr2 protein, ratUrocortinsamygdalaanxietyneuropeptidesocial interaction

Identifiers

PMID34487822
PMCPMC9744088
OpenAlexW3196960424

What OpenQuestion holds

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Registered trials

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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.