Evidence map›Paper›PMID 29383683›Full record

ArticleMolecular neurobiology2018

Disruption of A2AR-D2R Heteroreceptor Complexes After A2AR Transmembrane 5 Peptide Administration Enhances Cocaine Self-Administration in Rats.

Dasiel O Borroto-Escuela, Karolina Wydra, Xiang Li, David Rodriguez, Jens Carlsson, Joanna Jastrzębska, Malgorzata Filip, Kjell Fuxe

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 54 citations in OpenAlex.

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  15. Allosteric Interactions between Adenosine AInternational journal of molecular sciences · 2021
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  18. Adenosine ACells · 2020
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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

8 authors at 5 institutions in 5 countries.

Dasiel O Borroto-EscuelaDepartment of Neuroscience, Karolinska Institutet, Retzius väg 8, 17177, Stockholm, Sweden.
Karolina WydraInstitute of Pharmacology, Department of Drug Addiction Pharmacology, Polish Academy of Sciences, 12 Smetna Street, 31-343, Kraków, Poland.
Xiang LiDepartment of Neuroscience, Karolinska Institutet, Retzius väg 8, 17177, Stockholm, Sweden.
David RodriguezScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, SE-106 91, Stockholm, Sweden.
Jens CarlssonScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, SE-106 91, Stockholm, Sweden.
Joanna JastrzębskaInstitute of Pharmacology, Department of Drug Addiction Pharmacology, Polish Academy of Sciences, 12 Smetna Street, 31-343, Kraków, Poland.
Malgorzata FilipInstitute of Pharmacology, Department of Drug Addiction Pharmacology, Polish Academy of Sciences, 12 Smetna Street, 31-343, Kraków, Poland.
Kjell FuxeDepartment of Neuroscience, Karolinska Institutet, Retzius väg 8, 17177, Stockholm, Sweden. Kjell.Fuxe@ki.se.ORCID http://orcid.org/0000-0002-5736-373X
Maj Institute of Pharmacology · PLStockholm University · SEJilin University · CNKarolinska Institutet · SEUniversity of Urbino · IT

Funding

AFA Försäkring 130328Hjärnfonden FO2016-0302Karolinska Institutet Forskningsstiftelser 2016-2017Vetenskapsrådet 2013-5708Vetenskapsrådet 62X-00715-50-3
6 · The paper itself

Abstract

Antagonistic allosteric A2AR-D2R receptor-receptor interactions in heteroreceptor complexes counteract cocaine self-administration and cocaine seeking in rats as seen in biochemical and behavioral experiments. It was shown that the human A2AR transmembrane five (TM5) was part of the interface of the human A2AR-D2R receptor heteromer. In the current paper, the rat A2AR synthetic TM5 (synthTM5) peptide disrupts the A2AR-D2R heteroreceptor complex in HEK293 cells as shown by the bioluminescence resonance energy transfer method. Rat A2AR synthTM5 peptide, microinjected into the nucleus accumbens, produced a complete counteraction of the inhibitory effects of the A2AR agonist CGS21680 on cocaine self-administration. It was linked to a disappearance of the accumbal A2AR-D2R heteroreceptor complexes and the A2AR agonist induced inhibition of D2R recognition using proximity ligation assay and biochemical binding techniques. However, possible effects of the A2AR synthTM5 peptide on accumbal A2AR-D3R and A2AR-D4R heteroreceptor complexes remain to be excluded. Evidence is provided that accumbal A2AR-D2R-like heteroreceptor complexes with their antagonistic receptor-receptor interactions can be major targets for treatment of cocaine use disorder.

Indexed as

Amino Acid SequenceAnimalsCocaineDNA, ComplementaryFluorescence Resonance Energy TransferHEK293 CellsHumansMalePeptidesRats, Sprague-DawleyReceptor, Adenosine A2AReceptors, Dopamine D2Self AdministrationCocaineDNA, ComplementaryPeptidesReceptor, Adenosine A2AReceptors, Dopamine D2Adenosine A2A receptorCocaine self-administrationDimerizationDopamine D2 receptorHeteroreceptor complexesInterfering peptidesSubstance use disorder

Identifiers

PMID29383683
PMCPMC6061166
OpenAlexW2793853342

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.