Evidence map›Paper›PMID 35140231›Full record

ArticleNature communications2022

A diencephalic circuit in rats for opioid analgesia but not positive reinforcement.

Maggie W Waung, Kayla A Maanum, Thomas J Cirino, Joseph R Driscoll, Chris O'Brien, Svetlana Bryant, Kasra A Mansourian, Marisela Morales, David J Barker, Elyssa B Margolis

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 20 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

10 authors at 3 institutions in 1 country.

Maggie W WaungUCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.
Kayla A MaanumUCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.
Thomas J CirinoUCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.
Joseph R DriscollUCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.
Chris O'BrienDepartment of Psychology, Rutgers University, New Brunswick, NJ, USA.ORCID http://orcid.org/0000-0001-8533-658X
Svetlana BryantDepartment of Psychology, Rutgers University, New Brunswick, NJ, USA.
Kasra A MansourianUCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.
Marisela MoralesNational Institute on Drug Abuse, Neuronal Networks Section, National Institutes of Health, Baltimore, MD, USA.ORCID http://orcid.org/0000-0002-3845-9402
David J BarkerDepartment of Psychology, Rutgers University, New Brunswick, NJ, USA.
Elyssa B MargolisUCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA. Elyssa.Margolis@ucsf.edu.ORCID http://orcid.org/0000-0001-8777-302X
University of California, San Francisco · USRutgers, The State University of New Jersey · USNational Institutes of Health · US

Funding

The role of the VTA-lateral habenula circuit in opioid mediated behaviorsR01DA042025 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARGOLIS, ELYSSA · 2017 to 2021
$1.8M
Defining the differential roles of Glutamatergic and GABAergic projections from the Lateral Preoptic Area to the Lateral Habenula in Reward, Aversion, and Drug-Seeking Behavior.R00DA043572 · NIDA · RUTGERS, THE STATE UNIV OF N.J. · PI BARKER, DAVID J · 2019 to 2021
$747k
The Role of Mesencephalic Circuits in MigraineK08NS097632 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WAUNG, MAGGIE W · 2017 to 2020
$637k
NIDA NIH HHS K99 DA043572NIDA NIH HHS R00 DA043572NIDA NIH HHS R01 DA042025NINDS NIH HHS K08 NS097632
6 · The paper itself

Abstract

Mu opioid receptor (MOR) agonists are potent analgesics, but also cause sedation, respiratory depression, and addiction risk. The epithalamic lateral habenula (LHb) signals aversive states including pain, and here we found that it is a potent site for MOR-agonist analgesia-like responses in rats. Importantly, LHb MOR activation is not reinforcing in the absence of noxious input. The LHb receives excitatory inputs from multiple sites including the ventral tegmental area, lateral hypothalamus, entopeduncular nucleus, and the lateral preoptic area of the hypothalamus (LPO). Here we report that LHb-projecting glutamatergic LPO neurons are excited by noxious stimulation and are preferentially inhibited by MOR selective agonists. Critically, optogenetic stimulation of LHb-projecting LPO neurons produces an aversive state that is relieved by LHb MOR activation, and optogenetic inhibition of LHb-projecting LPO neurons relieves the aversiveness of ongoing pain.

Indexed as

Analgesics, OpioidReinforcement, PsychologyAnalgesiaAnimalsFemaleHabenulaHyperalgesiaHypothalamic Area, LateralMaleNeural PathwaysNeuronsPreoptic AreaRatsReceptors, Opioid, muVentral Tegmental AreaAnalgesics, OpioidReceptors, Opioid, mu

Identifiers

PMID35140231
PMCPMC8828762
OpenAlexW4210915051

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.