Evidence map›Paper›PMID 32210746›Full record

ArticleFrontiers in neuroscience2020

A Feasibility Study to Investigate Chemogenetic Modulation of the Locus Coeruleus by Means of Single Unit Activity.

Latoya Stevens, Kristl Vonck, Lars Emil Larsen, Wouter Van Lysebettens, Charlotte Germonpré, Veerle Baekelandt, Chris Van den Haute, Evelien Carrette, Wytse Jan Wadman, Paul Boon and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Latoya Stevens4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Kristl Vonck4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Lars Emil Larsen4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Wouter Van Lysebettens4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Charlotte Germonpré4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Veerle BaekelandtLaboratory for Neurobiology and Gene Therapy, Center for Molecular Medicine, Leuven Brain Institute, KU Leuven, Leuven, Belgium.
Chris Van den HauteLaboratory for Neurobiology and Gene Therapy, Center for Molecular Medicine, Leuven Brain Institute, KU Leuven, Leuven, Belgium.
Evelien Carrette4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Wytse Jan Wadman4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Paul Boon4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Robrecht Raedt4BRAIN, Institute for Neuroscience, Department of Neurology, Ghent University, Ghent, Belgium.
Ghent University · BEKU Leuven · BEVIB-KU Leuven Center for Brain & Disease Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimSelective chemogenetic modulation of locus coeruleus (LC) neurons would allow dedicated investigation of the role of the LC-NA pathway in brain excitability and disorders such as epilepsy. This study investigated the feasibility of an experimental set-up where chemogenetic modification of the brainstem locus coeruleus NA neurons is aimed at and followed by LC unit activity recording in response to clozapine.

methodsThe LC of male Sprague-Dawley rats was injected with 10 nl of adeno-associated viral vector AAV2/7-PRSx8-hM3Dq-mCherry (

resultsUnit recordings could be performed in 12 rats and in a total of 12 neurons (DREADDs:

conclusionLC unit recording is feasible in an experimental set-up following manipulations for DREADD induction. A relatively low transduction efficiency of the used AAV was found. In view of this finding, the effect of injected clozapine on LC-NA could not be investigated as a reliable outcome parameter for activation of chemogenetically modified LC neurons. The use of AAV2/7, a vector previously applied successfully to target dopaminergic neurons in the substantia nigra, leads to insufficient chemogenetic modification of the LC compared to transduction with AAV2/9.

Indexed as

chemogeneticsclozapinedesigner receptor exclusively activated by designer drugslocus coeruleusunit recordingvagus nerve stimulation

Identifiers

PMID32210746
PMCPMC7067893
OpenAlexW3009565234

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.