Evidence map›Paper›PMID 22434189›Full record

ArticleNature communications2012

Transient activation of specific neurons in mice by selective expression of the capsaicin receptor.

Ali D Güler, Aundrea Rainwater, Jones G Parker, Graham L Jones, Emanuela Argilli, Benjamin R Arenkiel, Michael D Ehlers, Antonello Bonci, Larry S Zweifel, Richard D Palmiter

Abstract read
In one paragraph

Article in Nature communications, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. The effect of selective nigrostriatal dopamine excess on behaviors linked to the cognitive and negative symptoms of schizophrenia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  8. Article
  9. Dopamine systems and biological rhythms: Let's get a move on.Frontiers in integrative neuroscience · 2022
    Review
  10. Article
  11. ACS chemical neuroscience · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

10 authors.

Ali D GülerHoward Hughes Medical Institute and Department of Biochemistry, University of Washington, 1959 NE Pacific Street, Box 357370, Seattle, Washington 98195, USA.
Aundrea Rainwater
Jones G Parker
Graham L Jones
Emanuela Argilli
Benjamin R Arenkiel
Michael D Ehlers
Antonello Bonci
Larry S Zweifel
Richard D Palmiter

Funding

Phasic Dopamine and Symptom Domains of Mental IllnessR01MH104450 · NIMH · UNIVERSITY OF WASHINGTON · PI LARRY S ZWEIFEL · 2015 to 2026
$5.5M
MAPPING CONNECTIVITY ONTO POSTNATAL-BORN NEURONSR01NS078294 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI ARENKIEL, BENJAMIN R · 2012 to 2023
$3.6M
The molecular basis of emotional learningP30MH089887 · NIMH · UNIVERSITY OF WASHINGTON · PI NEUMAIER, JOHN F · 2009 to 2010
$1.4M
Non-invasive Chemical Genetic Control of Neuronal ActivityR01MH086339 · NIMH · DUKE UNIVERSITY · PI EHLERS, MICHAEL D · 2009 to 2011
$776k
Activity Influence on Adult-Born Neuron Circuit IntegrationR00NS064171 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI ARENKIEL, BENJAMIN R · 2011 to 2013
$726k
Intramural NIH HHSNIMH NIH HHS P30 MH089887NIMH NIH HHS P30MH089887NIMH NIH HHS R01 MH086339NIMH NIH HHS R01MH086339NIMH NIH HHS R01 MH104450NINDS NIH HHS R00 NS064171NINDS NIH HHS R00NS064171NINDS NIH HHS R01 NS078294
6 · The paper itself

Abstract

The ability to control the electrical activity of a neuronal subtype is a valuable tool in deciphering the role of discreet cell populations in complex neural circuits. Recent techniques that allow remote control of neurons are either labor intensive and invasive or indirectly coupled to neural electrical potential with low temporal resolution. Here we show the rapid, reversible and direct activation of genetically identified neuronal subpopulations by generating two inducible transgenic mouse models. Confined expression of the capsaicin receptor, TRPV1, allows cell-specific activation after peripheral or oral delivery of ligand in freely moving mice. Capsaicin-induced activation of dopaminergic or serotonergic neurons reversibly alters both physiological and behavioural responses within minutes, and lasts ~10 min. These models showcase a robust and remotely controllable genetic tool that modulates a distinct cell population without the need for invasive and labour-intensive approaches.

Indexed as

Action PotentialsAnimalsCapsaicinDopamineDopaminergic NeuronsElectric StimulationFemaleMaleMiceMice, Inbred C57BLMice, TransgenicPatch-Clamp TechniquesSerotonergic NeuronsTRPV Cation ChannelsCapsaicinDopamineTRPV Cation Channels

Identifiers

PMID22434189
PMCPMC3592340

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.