Evidence map›Paper›PMID 35883437›Full record

ArticleBiomolecules2022

A Novel and Selective Dopamine Transporter Inhibitor,

Shima Kouhnavardi, Alev Ecevitoglu, Vladimir Dragačević, Fabrizio Sanna, Edgar Arias-Sandoval, Predrag Kalaba, Michael Kirchhofer, Jana Lubec, Marco Niello, Marion Holy and 15 more

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  4. Potential therapeutics for effort-related motivational dysfunction: assessing novel atypical dopamine transport inhibitors.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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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

25 authors at 7 institutions in 5 countries.

Shima KouhnavardiProgramme for Proteomics, Paracelsus Medical University, 5020 Salzburg, Austria.
Alev EcevitogluDepartment of Psychological Sciences, University of Connecticut, Storrs, CT 06269-1020, USA.
Vladimir DragačevićDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, 1090 Vienna, Austria.
Fabrizio SannaDepartment of Biomedical Sciences, Division of Neuroscience and Clinical Pharmacology, University of Cagliari, 09100 Cagliari, Italy.ORCID 0000-0002-9923-4231
Edgar Arias-SandovalDepartment of Psychobiology, Universitat Jaume I, 12071 Castellón de la Plana, Spain.ORCID 0000-0002-5943-1708
Predrag KalabaProgramme for Proteomics, Paracelsus Medical University, 5020 Salzburg, Austria.
Michael KirchhoferDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, 1090 Vienna, Austria.
Jana LubecProgramme for Proteomics, Paracelsus Medical University, 5020 Salzburg, Austria.
Marco NielloInstitute of Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-0518-5791
Marion HolyInstitute of Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.
Martin ZehlDepartment of Analytical Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.ORCID 0000-0001-9685-0373
Matthias PillweinProgramme for Proteomics, Paracelsus Medical University, 5020 Salzburg, Austria.
Judith WackerligDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, 1090 Vienna, Austria.
Rita MurauCenter for Behavioral Brain Sciences, Institut für Biochemie und Zellbiologie, Otto-von-Guericke-Universität Magdeburg, 39120 Magdeburg, Germany.
Andrea MohrmannCenter for Behavioral Brain Sciences, Institut für Biochemie und Zellbiologie, Otto-von-Guericke-Universität Magdeburg, 39120 Magdeburg, Germany.
Kathryn R BeardDepartment of Psychological Sciences, University of Connecticut, Storrs, CT 06269-1020, USA.
Harald H SitteInstitute of Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-1339-7444
Ernst UrbanDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, 1090 Vienna, Austria.
Claudia SaghedduDepartment of Biomedical Sciences, Division of Neuroscience and Clinical Pharmacology, University of Cagliari, 09100 Cagliari, Italy.ORCID 0000-0002-5315-2898
Marco PistisDepartment of Biomedical Sciences, Division of Neuroscience and Clinical Pharmacology, University of Cagliari, 09100 Cagliari, Italy.ORCID 0000-0002-4622-3205
Roberto PlasenzottiDivision of Biomedical Research, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0001-7652-1249
John D SalamoneDepartment of Psychological Sciences, University of Connecticut, Storrs, CT 06269-1020, USA.
Thierry LangerDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, 1090 Vienna, Austria.
Gert LubecProgramme for Proteomics, Paracelsus Medical University, 5020 Salzburg, Austria.
Francisco J MonjeCenter for Physiology and Pharmacology, Department of Neurophysiology and Neuropharmacology, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-6496-0030
University of Vienna · ATMedical University of Vienna · ATUniversity of Cagliari · ITUniversity of Connecticut · USCenter for Behavioral Brain Sciences · DEParacelsus Medical University · ATUniversitat Jaume I · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dopamine (DA), the most abundant human brain catecholaminergic neurotransmitter, modulates key behavioral and neurological processes in young and senescent brains, including motricity, sleep, attention, emotion, learning and memory, and social and reward-seeking behaviors. The DA transporter (DAT) regulates transsynaptic DA levels, influencing all these processes. Compounds targeting DAT (e.g., cocaine and amphetamines) were historically used to shape mood and cognition, but these substances typically lead to severe negative side effects (tolerance, abuse, addiction, and dependence). DA/DAT signaling dysfunctions are associated with neuropsychiatric and progressive brain disorders, including Parkinson's and Alzheimer diseases, drug addiction and dementia, resulting in devastating personal and familial concerns and high socioeconomic costs worldwide. The development of low-side-effect, new/selective medicaments with reduced abuse-liability and which ameliorate DA/DAT-related dysfunctions is therefore crucial in the fields of medicine and healthcare. Using the rat as experimental animal model, the present work describes the synthesis and pharmacological profile of (

Indexed as

DopamineDopamine Plasma Membrane Transport ProteinsAnimalsHippocampusHumansMotivationNeuronal PlasticityRatsDopamineDopamine Plasma Membrane Transport Proteinsdopaminedopamine transportereffort-related behavioremotional behaviorhippocampuslearning and memorymodafinilsynaptic plasticity

Identifiers

PMID35883437
PMCPMC9312958
OpenAlexW4283451750

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.