Evidence map›Paper›PMID 24937095›Full record

ArticleTranslational psychiatry2014

Implication of dopamine D3 receptor activation in the reversion of Parkinson's disease-related motivational deficits.

S Carnicella, G Drui, S Boulet, C Carcenac, M Favier, T Duran, M Savasta

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.0field-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

31 citing papers in PubMed, 75 citations in OpenAlex.

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  15. Risk of Drug-induced Movement Disorders with Newer Antipsychotic Agents.Tremor and other hyperkinetic movements (New York, N.Y.) · 2022
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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

7 authors at 2 institutions in 1 country.

S Carnicella1] Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Equipe 10, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France [2] Grenoble University, Grenoble, France.
G Drui1] Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Equipe 10, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France [2] Grenoble University, Grenoble, France.
S Boulet1] Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Equipe 10, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France [2] Grenoble University, Grenoble, France.
C Carcenac1] Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Equipe 10, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France [2] Grenoble University, Grenoble, France.
M Favier1] Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Equipe 10, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France [2] Grenoble University, Grenoble, France.
T Duran1] Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Equipe 10, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France [2] Grenoble University, Grenoble, France.
M Savasta1] Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Equipe 10, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France [2] Grenoble University, Grenoble, France [3] Department of Neurology and Psychiatry, Centre Hospitalier Universitaire de Grenoble, BP217, Grenoble, France.
Grenoble Institute of Neurosciences · FRUniversité Grenoble Alpes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to the classical motor symptoms, motivational and affective deficits are core impairments of Parkinson's disease (PD). We recently demonstrated, by lesional approaches in rats, that degeneration of the substantia nigra pars compacta (SNc) dopaminergic (DA) neurons is likely to have a crucial role in the development of these neuropsychiatry symptoms. We have also shown that, as in clinical investigations, chronic treatment with levodopa or the DA D2/D3 receptor (D2/D3R) agonist ropinirole specifically reverses these PD-related motivational deficits. The roles of specific DA receptor subtypes in such reversal effects remain, however, unknown. We therefore investigated here the precise involvement of D1, D2 and D3R in the reversal of the motivational and affective deficits related to SNc DA neuronal loss. Three weeks after bilateral and partial 6-hydroxydopamine (6-OHDA) SNc lesions, rats received 14 daily intraperitoneal administrations of the selective D1R agonist SKF-38393 (2.5 or 3.5 mg kg(-1)), the selective D2R agonist sumanirole (0.1 or 0.15 mg kg(-1)), or the preferring D3R gonist PD-128907 (0.1 or 0.15 mg kg(-1)). Anxiety-, depressive-like and motivated behaviors were assessed in an elevated-plus maze, a forced-swim test, and an operant sucrose self-administration procedure, respectively. All DA agonists attenuated anxiety- and depressive-like behaviors. However, only PD-128907 reversed the motivational deficits induced by 6-OHDA SNc lesions. This effect was blocked by a selective D3R (SB-277011A, 10 mg kg(-1)), but not D2R (L-741,626, 1.5 mg kg(-1)), antagonist. These data provide strong evidence for the role of D3R in motivational processes and identify this receptor as a potentially valuable target for the treatment of PD-related neuropsychiatric symptoms.

Indexed as

AnimalsBehavior, AnimalDisease Models, AnimalDopamine AgonistsDopamine AntagonistsDopaminergic NeuronsMotivationParkinson DiseaseRatsReceptors, Dopamine D1Receptors, Dopamine D2Receptors, Dopamine D3Substantia NigraDopamine AgonistsDopamine AntagonistsReceptors, Dopamine D1Receptors, Dopamine D2Receptors, Dopamine D3

Identifiers

PMID24937095
PMCPMC4080324
OpenAlexW2123599105

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.