Evidence map›Paper›PMID 21389985›Full record

ArticleNature2011

Amygdala circuitry mediating reversible and bidirectional control of anxiety.

Kay M Tye, Rohit Prakash, Sung-Yon Kim, Lief E Fenno, Logan Grosenick, Hosniya Zarabi, Kimberly R Thompson, Viviana Gradinaru, Charu Ramakrishnan, Karl Deisseroth

Open access · greenAbstract read
In one paragraph

Article in Nature, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 725 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
725citing papers in PubMed, 1 pooled it
35.0field-weighted citation impact, top 1% 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

725 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,288 citations in OpenAlex.

  1. Pooled it
  2. Review
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  15. Identification of somatostatinProceedings of the National Academy of Sciences of the United States of America · 2026
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  17. Negative-Valence Neurons in the Larval Zebrafish Pallium.bioRxiv : the preprint server for biology · 2026
    Article
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  20. Review

665 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

Kay M TyeDepartment of Bioengineering, Stanford University, Stanford, California 94305, USA.
Rohit Prakash
Sung-Yon Kim
Lief E Fenno
Logan Grosenick
Hosniya Zarabi
Kimberly R Thompson
Viviana Gradinaru
Charu Ramakrishnan
Karl Deisseroth
Stanford University · US

Funding

Calcium channels, newborn neurons, and CNS circuit dynamicsR01DA020794 · NIDA · STANFORD UNIVERSITY · PI DEISSEROTH, KARL A. · 2005 to 2014
$4.1M
NIH Director's Pioneer Award (RMI)DP1OD000616 · OD · STANFORD UNIVERSITY · PI DEISSEROTH, KARL A. · 2005 to 2009
$3.8M
A Novel Strategy for Combating Obesity: Reprogramming Neural CircuitsDP2DK102256 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI TYE, KAY MAXINE · 2013 to 2018
$2.7M
Technology development for fast optical interrogation of living neural circuitryR01MH075957 · NIMH · STANFORD UNIVERSITY · PI DEISSEROTH, KARL A. · 2008 to 2012
$2.6M
The effects of thalamoamygdalar synaptic potentiation on learning performanceF32MH088010 · NIMH · STANFORD UNIVERSITY · PI TYE, KAY MAXINE · 2009 to 2011
$120k
NIDA NIH HHS R01 DA020794NIDDK NIH HHS DP2 DK102256NIH HHS DP1 OD000616NIMH NIH HHS 1F32MH088010-01NIMH NIH HHS F32 MH088010NIMH NIH HHS R01 MH075957
6 · The paper itself

Abstract

Anxiety--a sustained state of heightened apprehension in the absence of immediate threat--becomes severely debilitating in disease states. Anxiety disorders represent the most common of psychiatric diseases (28% lifetime prevalence) and contribute to the aetiology of major depression and substance abuse. Although it has been proposed that the amygdala, a brain region important for emotional processing, has a role in anxiety, the neural mechanisms that control anxiety remain unclear. Here we explore the neural circuits underlying anxiety-related behaviours by using optogenetics with two-photon microscopy, anxiety assays in freely moving mice, and electrophysiology. With the capability of optogenetics to control not only cell types but also specific connections between cells, we observed that temporally precise optogenetic stimulation of basolateral amygdala (BLA) terminals in the central nucleus of the amygdala (CeA)--achieved by viral transduction of the BLA with a codon-optimized channelrhodopsin followed by restricted illumination in the downstream CeA--exerted an acute, reversible anxiolytic effect. Conversely, selective optogenetic inhibition of the same projection with a third-generation halorhodopsin (eNpHR3.0) increased anxiety-related behaviours. Importantly, these effects were not observed with direct optogenetic control of BLA somata, possibly owing to recruitment of antagonistic downstream structures. Together, these results implicate specific BLA-CeA projections as critical circuit elements for acute anxiety control in the mammalian brain, and demonstrate the importance of optogenetically targeting defined projections, beyond simply targeting cell types, in the study of circuit function relevant to neuropsychiatric disease.

Indexed as

AmygdalaAnimalsAnxietyAnxiety DisordersHalorhodopsinsLightMiceModels, NeurologicalNeural PathwaysNeuronsStress, PhysiologicalSynapsesHalorhodopsins

Identifiers

PMID21389985
PMCPMC3154022
OpenAlexW2060978874

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.