Evidence map›Paper›PMID 26979295›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

Antidepressant-like Effects of Buprenorphine are Mediated by Kappa Opioid Receptors.

Edgardo Falcon, Caroline A Browne, Rosa M Leon, Vanessa C Fleites, Rachel Sweeney, Lynn G Kirby, Irwin Lucki

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 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 119 citations in OpenAlex.

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  18. Delta Opioid Receptor-Mediated Antidepressant-Like Effects of Diprenorphine in Mice.The Journal of pharmacology and experimental therapeutics · 2023
    Article
  19. Negative allosteric modulation of CBPharmacological research · 2022
    Article
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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

7 authors at 2 institutions in 1 country.

Edgardo FalconDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Caroline A BrowneDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Rosa M LeonDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Vanessa C FleitesDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Rachel SweeneyDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Lynn G KirbyDepartment of Pharmacology, Temple University School of Medicine, Philadelphia, PA, USA.
Irwin LuckiDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
University of Pennsylvania · USTemple University · US

Funding

Pilot Projects Core (PPC)P30DA013429 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI Munir Gunes Kutlu · 2000 to 2026
$34.6M
TRAINING PROGRAM IN NEUROPSYCHOPHARMACOLOGY-PREDOCTORALT32MH014654 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BERRETTINI, WADE H · 1985 to 2021
$5.0M
Buprenorphine for Depression and AnxietyR01MH092412 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI LUCKI, IRWIN · 2012 to 2016
$2.0M
NIDA NIH HHS P30 DA013429NIMH NIH HHS R01 MH092412NIMH NIH HHS T32 MH014654
6 · The paper itself

Abstract

Previous studies have identified potential antidepressant effects of buprenorphine (BPN), a drug with high affinity for mu opioid receptor (MORs) and kappa opioid receptors (KORs) and some affinity at delta opioid receptor (DOR) and opioid receptor-like 1 (ORL-1) receptors. Therefore, these studies examined which opioid receptors were involved in BPN's effects on animal behavior tests sensitive to antidepressant drugs. The acute effects of BPN were tested in the forced swim test (FST) using mice with genetic deletion of individual opioid receptors or after pharmacological blockade of receptors. For evaluating the effects of BPN on chronic stress, separate groups of mice were exposed to unpredictable chronic mild stress (UCMS) for 3 weeks and treated with BPN for at least 7 days before behavioral assessment and subsequent measurement of Oprk1, Oprm1, and Pdyn mRNA expression in multiple brain regions. BPN did not reduce immobility in mice with KOR deletion or after pretreatment with norbinaltorphimine, even though desipramine remained effective. In contrast, BPN reduced immobility in MOR and DOR knockout mice and in mice pretreated with the ORL-1 antagonist JTC-801. UCMS reduced sucrose preference, decreased time in the light side of the light/dark box, increased immobility in the FST and induced region-specific alterations in Oprk1, Oprm1, and PDYN mRNA expression in the frontal cortex and striatum. All of these changes were normalized following BPN treatment. The KOR was identified as a key player mediating the effects of BPN in tests sensitive to antidepressant drugs in mice. These studies support further development of BPN as a novel antidepressant.

Indexed as

AnimalsAntidepressive AgentsBehavior, AnimalBrainBuprenorphineMaleMice, Inbred C57BLMice, KnockoutReceptors, Opioid, deltaReceptors, Opioid, kappaReceptors, Opioid, muStress, PsychologicalAntidepressive AgentsBuprenorphineReceptors, Opioid, deltaReceptors, Opioid, kappaReceptors, Opioid, mu

Identifiers

PMID26979295
PMCPMC4946065
OpenAlexW2306924576

What OpenQuestion holds

Textmetadata
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.