Evidence map›Paper›PMID 15901780›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Regulation of alpha-synuclein expression in limbic and motor brain regions of morphine-treated mice.

Barbara Ziolkowska, Agnieszka Gieryk, Wiktor Bilecki, Agnieszka Wawrzczak-Bargiela, Krzysztof Wedzony, Agnieszka Chocyk, Patria E Danielson, Elizabeth A Thomas, Brian S Hilbush, J Gregor Sutcliffe and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-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

16 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Morphine Antidependence ofEvidence-based complementary and alternative medicine : eCAM · 2016
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. 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

11 authors at 4 institutions in 2 countries.

Barbara ZiolkowskaInstitute of Pharmacology, Polish Academy of Sciences, 31-343 Kraków, Poland.
Agnieszka Gieryk
Wiktor Bilecki
Agnieszka Wawrzczak-Bargiela
Krzysztof Wedzony
Agnieszka Chocyk
Patria E Danielson
Elizabeth A Thomas
Brian S Hilbush
J Gregor Sutcliffe
Ryszard Przewlocki
Polish Academy of Sciences · PLScripps Research Institute · USMaj Institute of Pharmacology · PLMarker Gene Technologies (United States) · US

Funding

GENE EXPRESSION IN RAT BRAINR01GM032355 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SUTCLIFFE, J GREGOR · 1985 to 2010
$4.2M
NIGMS NIH HHS GM32355NIGMS NIH HHS R01 GM032355
6 · The paper itself

Abstract

Chronic exposure to opiates produces dependence and addiction, which may result from neuroadaptations in the dopaminergic reward pathway and its target brain regions. The neuronal protein alpha-synuclein has been implicated in neuronal plasticity and proposed to serve as a negative regulator of dopamine neurotransmission. Thus, alpha-synuclein could mediate some effects of opiates in the brain. The present study investigated the influence of acute and chronic morphine administration on alpha-synuclein mRNA and protein expression in the brains of mice. Downregulation of alpha-synuclein mRNA was observed in the basolateral amygdala, dorsal striatum, nucleus accumbens, and ventral tegmental area of mice withdrawn from chronic morphine treatment. The changes were the most pronounced after longer periods of withdrawal (48 h). In contrast, levels of alpha-synuclein protein, as assessed by Western blotting, were significantly increased in the amygdala and striatum/accumbens (but not in the mesencephalon) of morphine-withdrawn mice. In both brain regions, levels of alpha-synuclein were elevated for as long as 2 weeks after treatment cessation. Because alpha-synuclein is a presynaptic protein, the detected opposite changes in its mRNA and protein levels are likely to take place in different populations of projection neurons whose somata are in different brain areas. Axonal localization of alpha-synuclein was confirmed by immunofluorescent labeling. An attempt to identify postsynaptic neurons innervated by alpha-synuclein-containing axon terminals revealed their selective apposition to calbindin D28K-negative projection neurons in the basolateral amygdala. The observed changes in alpha-synuclein levels are discussed in connection with their putative role in mediating suppression of dopaminergic neurotransmission during opiate withdrawal.

Indexed as

alpha-SynucleinAnalysis of VarianceAnimalsBlotting, WesternDiagnostic ImagingDrug Administration ScheduleGene Expression RegulationImmunohistochemistryIn Situ HybridizationLimbic SystemMaleMiceMice, Inbred C57BLMorphineNarcoticsReverse Transcriptase Polymerase Chain Reactionalpha-SynucleinMorphineNarcoticsRNA, Messenger

Identifiers

PMID15901780
PMCPMC6724864
OpenAlexW2170070931

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.