Evidence map›Paper›PMID 32770257›Full record

ArticlePsychopharmacology2020

Behavioral and dopamine transporter binding properties of the modafinil analog (S, S)-CE-158: reversal of the motivational effects of tetrabenazine and enhancement of progressive ratio responding.

Renee A Rotolo, Predrag Kalaba, Vladimir Dragacevic, Rose E Presby, Julia Neri, Emily Robertson, Jen-Hau Yang, Merce Correa, Vasiliy Bakulev, Natalia N Volkova and 3 more

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  7. 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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  20. Vigor, Effort-Related Aspects of Motivation and Anhedonia.Current topics in behavioral neurosciences · 2022
    Review
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

13 authors at 5 institutions in 4 countries.

Renee A RotoloDepartment of Psychological Sciences, University of Connecticut, Storrs, CT, USA.
Predrag KalabaDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, Althanstraße 14, 1090, Vienna, Austria.
Vladimir DragacevicDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, Althanstraße 14, 1090, Vienna, Austria.
Rose E PresbyDepartment of Psychological Sciences, University of Connecticut, Storrs, CT, USA.
Julia NeriDepartment of Psychological Sciences, University of Connecticut, Storrs, CT, USA.
Emily RobertsonDepartment of Psychological Sciences, University of Connecticut, Storrs, CT, USA.
Jen-Hau YangDepartment of Psychological Sciences, University of Connecticut, Storrs, CT, USA.
Merce CorreaDepartment of Psychological Sciences, University of Connecticut, Storrs, CT, USA.
Vasiliy BakulevUral Federal University named after the first President of Russia B. N.Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russia.
Natalia N VolkovaUral Federal University named after the first President of Russia B. N.Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russia.
Christian PiflCentre for Brain Research, Medical University of Vienna, Vienna, Austria.
Gert LubecDepartment of Neuroproteomics, Paracelsus Medical University, Salzburg, Austria. gert.lubec@lubeclab.com.
John D SalamoneDepartment of Psychological Sciences, University of Connecticut, Storrs, CT, USA. john.salamone@uconn.edu.
University of Connecticut · USUniversity of Vienna · ATUral Federal University · RUMedical University of Vienna · ATParacelsus Medical University · AT

Funding

Physiological markers of forebrain circuit engagement regulating effort-based decision making.R01MH121350 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI SALAMONE, JOHN D · 2019 to 2021
$1.2M
Development of rat models of the effort-related symptoms of depressionR03MH094966 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI SALAMONE, JOHN D · 2012 to 2013
$151k
NIMH NIH HHS R01 MH121350NIMH NIH HHS R03 MH094966
6 · The paper itself

Abstract

rationaleAtypical dopamine (DA) transport blockers such as modafinil and its analogs may be useful for treating motivational symptoms of depression and other disorders. Previous research has shown that the DA depleting agent tetrabenazine can reliably induce motivational deficits in rats, as evidenced by a shift towards a low-effort bias in effort-based choice tasks. This is consistent with human studies showing that people with major depression show a bias towards low-effort activities.

objectivesRecent studies demonstrated that the atypical DA transport (DAT) inhibitor (S)-CE-123 reversed tetrabenazine-induced motivational deficits, increased progressive ratio (PROG) lever pressing, and increased extracellular DA in the nucleus accumbens. In the present studies, a recently synthesized modafinil analog, (S, S)-CE-158, was assessed in a series of neurochemical and behavioral studies in rats.

results(S, S)-CE-158 demonstrated the ability to reverse the effort-related effects of tetrabenazine and increase selection of high-effort PROG lever pressing in rats tested on PROG/chow feeding choice task. (S, S)-CE-158 showed a high selectivity for inhibiting DAT compared with other monoamine transporters, and systemic administration of (S, S)-CE-158 increased extracellular DA in the nucleus accumbens during the behaviorally active time course, which is consistent with the effects of (S)-CE-123 and other DAT inhibitors that enhance high-effort responding.

conclusionsThese studies provide an initial neurochemical characterization of a novel atypical DAT inhibitor, and demonstrate that this compound is active in models of effort-related choice. This research could contribute to the development of novel compounds for the treatment of motivational dysfunctions in humans.

Indexed as

Adrenergic Uptake InhibitorsAnimalsChoice BehaviorDopamine Plasma Membrane Transport ProteinsDose-Response Relationship, DrugFeeding BehaviorHEK293 CellsHumansMaleModafinilMotivationNucleus AccumbensProtein BindingRatsRats, Sprague-DawleyTetrabenazineAdrenergic Uptake InhibitorsDopamine Plasma Membrane Transport ProteinsModafinilTetrabenazineAnergiaDepressionDopamineFatigueModafinilMotivationSynthesisTransport

Identifiers

PMID32770257
PMCPMC7572767
OpenAlexW3048315010

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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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.