Evidence map›Paper›PMID 18327293›Full record

ArticlePloS one2008

Endogenous morphine in SH-SY5Y cells and the mouse cerebellum.

Arnaud Muller, Elise Glattard, Omar Taleb, Véronique Kemmel, Alexis Laux, Monique Miehe, François Delalande, Guy Roussel, Alain Van Dorsselaer, Marie-Hélène Metz-Boutigue and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Morphine Binds Creatine Kinase B and Inhibits Its Activity.Frontiers in cellular neuroscience · 2018
    Article
  3. Article
  4. UDP-glucuronosyltransferase 1a enzymes are present and active in the mouse blastocyst.Drug metabolism and disposition: the biological fate of chemicals · 2014
    Article
  5. Review
  6. Article
  7. Article
  8. Urinary excretion of morphine and biosynthetic precursors in mice.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  9. Article
  10. Article
  11. 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

12 authors at 4 institutions in 1 country.

Arnaud MullerInserm, U575, Physiopathologie du Système Nerveux, Strasbourg, France.
Elise Glattard
Omar Taleb
Véronique Kemmel
Alexis Laux
Monique Miehe
François Delalande
Guy Roussel
Alain Van Dorsselaer
Marie-Hélène Metz-Boutigue
Dominique Aunis
Yannick Goumon
Inserm · FRNeuropsychologie Cognitive et Physiopathologie de la Schizophrénie · FRCentre National de la Recherche Scientifique · FRInstitut de Chimie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMorphine, the principal active agent in opium, is not restricted to plants, but is also present in different animal tissues and cell types, including the mammalian brain. In fact, its biosynthetic pathway has been elucidated in a human neural cell line. These data suggest a role for morphine in brain physiology (e.g., neurotransmission), but this hypothesis remains a matter of debate. Recently, using the adrenal neuroendocrine chromaffin cell model, we have shown the presence of morphine-6-glucuronide (M6G) in secretory granules and their secretion products, leading us to propose that these endogenous alkaloids might represent new neuroendocrine factors. Here, we investigate the potential function of endogenous alkaloids in the central nervous system. METHODOLOGY AND PRINCIPAL

findingsMicroscopy, molecular biology, electrophysiology, and proteomic tools were applied to human neuroblastoma SH-SY5Y cells (i) to characterize morphine and M6G, and (ii) to demonstrate the presence of the UDP-glucuronyltransferase 2B7 enzyme, which is responsible for the formation of M6G from morphine. We show that morphine is secreted in response to nicotine stimulation via a Ca(2+)-dependent mechanism involving specific storage and release mechanisms. We also show that morphine and M6G at concentrations as low as 10(-10) M are able to evoke specific naloxone-reversible membrane currents, indicating possible autocrine/paracrine regulation in SH-SY5Y cells. Microscopy and proteomic approaches were employed to detect and quantify endogenous morphine in the mouse brain. Morphine is present in the hippocampus, cortex, olfactory bulb, and cerebellum at concentration ranging from 1.45 to 7.5 pmol/g. In the cerebellum, morphine immunoreactivity is localized to GABA basket cells and their termini, which form close contacts on Purkinje cell bodies. CONCLUSIONS/SIGNIFICANCE: The presence of morphine in the brain and its localization in particular areas lead us to conclude that it has a specific function in neuromodulation and/or neurotransmission. Furthermore, its presence in cerebellar basket cell termini suggests that morphine has signaling functions in Purkinje cells that remain to be discovered.

Indexed as

Brain ChemistryAlkaloidsAnimalsCell Line, TumorCerebellumElectrophysiologyGlucuronosyltransferaseHumansMiceMorphineMorphine DerivativesNeuroblastomaPurkinje CellsSynaptic TransmissionAlkaloidsGlucuronosyltransferaseMorphinemorphine-6-glucuronideMorphine Derivatives

Identifiers

PMID18327293
PMCPMC2265639
OpenAlexW2086921213

What OpenQuestion holds

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LicenceCC BY
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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.