Evidence map›Paper›PMID 26390873›Full record

ArticleThe international journal of neuropsychopharmacology2016

Methadone Reverses Analgesic Tolerance Induced by Morphine Pretreatment.

Luca Posa, Alison Accarie, Florence Noble, Nicolas Marie

Open access · goldAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 24 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

4 authors at 2 institutions in 1 country.

Luca PosaCentre National de la Recherche Scientifique, Unité Mixte de Recherche, Paris, France; Institut national de la santé et de la recherche médicale, Paris, France; Université Paris Descartes, Laboratoire de Neuropsychopharmacologie des Addictions, Paris, France.
Alison AccarieCentre National de la Recherche Scientifique, Unité Mixte de Recherche, Paris, France; Institut national de la santé et de la recherche médicale, Paris, France; Université Paris Descartes, Laboratoire de Neuropsychopharmacologie des Addictions, Paris, France.
Florence NobleCentre National de la Recherche Scientifique, Unité Mixte de Recherche, Paris, France; Institut national de la santé et de la recherche médicale, Paris, France; Université Paris Descartes, Laboratoire de Neuropsychopharmacologie des Addictions, Paris, France. florence.noble@parisdescartes.fr.
Nicolas MarieCentre National de la Recherche Scientifique, Unité Mixte de Recherche, Paris, France; Institut national de la santé et de la recherche médicale, Paris, France; Université Paris Descartes, Laboratoire de Neuropsychopharmacologie des Addictions, Paris, France.
Université Paris Cité · FRDélégation Paris 5 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOpiates such as morphine are the most powerful analgesics, but their protracted use is restrained by the development of tolerance to analgesic effects. Recent works suggest that tolerance to morphine might be due to its inability to promote mu opioid receptor endocytosis, and the co-injection of morphine with a mu opioid receptor internalizing agonist like [D-Ala(2),N-Me-Phe(4),Gly-ol(5)]enkephalin reduces tolerance to morphine. So far, no studies have been conducted to evaluate the ability of methadone to reduce morphine tolerance in morphine-pretreated animals, a treatment sequence that could be encountered in opiate rotation protocol. We investigated the ability of methadone (a mu opioid receptor internalizing agonist used in therapy) to reverse morphine tolerance and the associated cellular mechanisms in the periaqueductal gray matter, a region involved in pain control.

methodsWe measured analgesic response following a challenge dose of morphine in the hot plate test and investigated regulation of mu opioid receptor (coupling and endocytosis) and some cellular mechanisms involved in tolerance such as adenylate cyclase superactivation and changes in N-methyl-d-aspartate receptor subunits expression and phosphorylation state.

resultsA chronic treatment with morphine promoted tolerance to its analgesic effects and was associated with a lack of mu opioid receptor endocytosis, adenylate cyclase overshoot, NR2A and NR2B downregulation, and phosphorylation of NR1. We reported that a methadone treatment in morphine-treated mice reversed morphine tolerance to analgesia by promoting mu opioid receptor endocytosis and blocking cellular mechanisms of tolerance.

conclusionsOur data might lead to rational strategies to tackle opiate tolerance in the frame of opiate rotation.

Indexed as

Drug ToleranceAdenylyl CyclasesAnalgesics, OpioidAnimalsDose-Response Relationship, DrugDown-RegulationEndocytosisMaleMethadoneMiceMorphinePain MeasurementPhosphorylationReceptors, N-Methyl-D-AspartateReceptors, Opioid, muAdenylyl CyclasesAnalgesics, OpioidMethadoneMorphineReceptors, N-Methyl-D-AspartateReceptors, Opioid, muadenylate cyclaseanalgesiaendocytosismethadonemorphinemu opioid receptorNMDA receptor

Identifiers

PMID26390873
PMCPMC4966270
OpenAlexW2285959938

What OpenQuestion holds

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LicenceCC BY-NC
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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.