Evidence map›Paper›PMID 26725834›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

Chemogenetic and Optogenetic Activation of Gαs Signaling in the Basolateral Amygdala Induces Acute and Social Anxiety-Like States.

Edward R Siuda, Ream Al-Hasani, Jordan G McCall, Dionnet L Bhatti, Michael R Bruchas

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Identification of a stress-responsive subregion of the basolateral amygdala in male rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
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  16. Wireless optoelectronic photometers for monitoring neuronal dynamics in the deep brain.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Article
  18. Review
  19. Gs/Gi Regulation of Bone Cell Differentiation: Review and Insights from Engineered Receptors.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2016
    Review
  20. Resolving Behavioral Output via Chemogenetic Designer Receptors Exclusively Activated by Designer Drugs.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    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

5 authors at 1 institution in 1 country.

Edward R SiudaDepartment of Anesthesiology, Division of Basic Research, Washington University School of Medicine, St Louis, Missouri, USA.
Ream Al-HasaniDepartment of Anesthesiology, Division of Basic Research, Washington University School of Medicine, St Louis, Missouri, USA.
Jordan G McCallDepartment of Anesthesiology, Division of Basic Research, Washington University School of Medicine, St Louis, Missouri, USA.ORCID 0000-0001-8295-0664
Dionnet L BhattiDepartment of Anesthesiology, Division of Basic Research, Washington University School of Medicine, St Louis, Missouri, USA.
Michael R BruchasDepartment of Anesthesiology, Division of Basic Research, Washington University School of Medicine, St Louis, Missouri, USA.
Washington University in St. Louis · US

Funding

Washington University Center for Translational NeuroscienceP30NS057105 · NINDS · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 2006 to 2011
$8.7M
WIRELESS IN VIVO OPTICAL CONTROL OF STRESS NEURAL CIRCUITS AND GPCR SIGNALINGR01DA037152 · NIDA · WASHINGTON UNIVERSITY · PI BRUCHAS, MICHAEL R. · 2013 to 2016
$1.2M
Opioid and Noradrenergic Mechanisms in Stress and Drug SeekingR00DA025182 · NIDA · WASHINGTON UNIVERSITY · PI BRUCHAS, MICHAEL R. · 2011 to 2013
$723k
LOCUS COERULEUS NEURAL CIRCUITS AND SIGNALING IN NOCICEPTION AND STRESSR21DA035144 · NIDA · WASHINGTON UNIVERSITY · PI BRUCHAS, MICHAEL R. · 2013 to 2014
$418k
DEFINING DYNORPHIN-CRF CIRCUITS IN STRESS AND NICOTINE BEHAVIORSK99DA038725 · NIDA · WASHINGTON UNIVERSITY · PI AL-HASANI, REAM · 2015 to 2016
$280k
Dissecting the role of locus coeruleus circuitry in anxiety-like behaviorsF31MH101956 · NIMH · WASHINGTON UNIVERSITY · PI MCCALL, JORDAN G. · 2013 to 2014
$56k
NIDA NIH HHS K99 DA038725NIDA NIH HHS R00 DA025182NIDA NIH HHS R01 DA037152NIDA NIH HHS R21 DA035144NIMH NIH HHS F31 MH101956NINDS NIH HHS P30 NS057105
6 · The paper itself

Abstract

Anxiety disorders are debilitating psychiatric illnesses with detrimental effects on human health. These heightened states of arousal are often in the absence of obvious threatening cues and are difficult to treat owing to a lack of understanding of the neural circuitry and cellular machinery mediating these conditions. Activation of noradrenergic circuitry in the basolateral amygdala is thought to have a role in stress, fear, and anxiety, and the specific cell and receptor types responsible is an active area of investigation. Here we take advantage of two novel cellular approaches to dissect the contributions of G-protein signaling in acute and social anxiety-like states. We used a chemogenetic approach utilizing the Gαs DREADD (rM3Ds) receptor and show that selective activation of generic Gαs signaling is sufficient to induce acute and social anxiety-like behavioral states in mice. Second, we use a recently characterized chimeric receptor composed of rhodopsin and the β2-adrenergic receptor (Opto-β2AR) with in vivo optogenetic techniques to selectively activate Gαs β-adrenergic signaling exclusively within excitatory neurons of the basolateral amygdala. We found that optogenetic induction of β-adrenergic signaling in the basolateral amygdala is sufficient to induce acute and social anxiety-like behavior. These findings support the conclusion that activation of Gαs signaling in the basolateral amygdala has a role in anxiety. These data also suggest that acute and social anxiety-like states may be mediated through signaling pathways identical to β-adrenergic receptors, thus providing support that inhibition of this system may be an effective anxiolytic therapy.

Indexed as

AnimalsAnxietyBasolateral Nuclear ComplexBehavior, AnimalGTP-Binding Protein alpha SubunitsHEK293 CellsHumansMaleMice, Inbred C57BLNeuronsOptogeneticsReceptors, Adrenergic, beta-2Signal TransductionSocial BehaviorGTP-Binding Protein alpha SubunitsReceptors, Adrenergic, beta-2

Identifiers

PMID26725834
PMCPMC4908638
OpenAlexW2224362692

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.