Evidence map›Paper›PMID 20236221›Full record

ArticleJournal of neurochemistry2010

Role of adrenoceptors in the regulation of dopamine/DARPP-32 signaling in neostriatal neurons.

Masato Hara, Ryuichi Fukui, Eriko Hieda, Mahomi Kuroiwa, Helen S Bateup, Tatsuhiko Kano, Paul Greengard, Akinori Nishi

Open access · greenAbstract read
In one paragraph

Article in Journal of neurochemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 58 citations in OpenAlex.

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  12. αMolecular neurobiology · 2018
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  17. Dopamine reverses reward insensitivity in apathy following globus pallidus lesions.Cortex; a journal devoted to the study of the nervous system and behavior · 2013
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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 2 institutions in 2 countries.

Masato HaraDepartment of Anesthesiology, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
Ryuichi Fukui
Eriko Hieda
Mahomi Kuroiwa
Helen S Bateup
Tatsuhiko Kano
Paul Greengard
Akinori Nishi
Kurume University · JPRockefeller University · US

Funding

THE ROLE OF DARPPS IN THE ACUTE AND CHRONIC EFFECTS OF COCAINE AND AMPHETAMINEP01DA010044 · NIDA · ROCKEFELLER UNIVERSITY · PI GREENGARD, PAUL · 1996 to 2015
$23.6M
Transgenic Core - Greengard (pgs. 218 - 235)P50MH074866 · NIMH · ROCKEFELLER UNIVERSITY · PI GREENGARD, PAUL · 2005 to 2009
$11.6M
NIDA NIH HHS DA10044NIDA NIH HHS P01 DA010044NIMH NIH HHS MH074866NIMH NIH HHS P50 MH074866
6 · The paper itself

Abstract

Studies in animal models of Parkinson's disease have revealed that degeneration of noradrenaline neurons is involved in the motor deficits. Several types of adrenoceptors are highly expressed in neostriatal neurons. However, the selective actions of these receptors on striatal signaling pathways have not been characterized. In this study, we investigated the role of adrenoceptors in the regulation of dopamine/dopamine- and cAMP-regulated phosphoprotein of M(r) 32 kDa (DARPP-32) signaling by analyzing DARPP-32 phosphorylation at Thr34 [protein kinase A (PKA)-site] in mouse neostriatal slices. Activation of beta(1)-adrenoceptors induced a rapid and transient increase in DARPP-32 phosphorylation. Activation of alpha(2)-adrenoceptors also induced a rapid and transient increase in DARPP-32 phosphorylation, which subsequently decreased below basal levels. In addition, activation of alpha(2)-adrenoceptors attenuated, and blockade of alpha(2)-adrenoceptors enhanced dopamine D(1) and adenosine A(2A) receptor/DARPP-32 signaling. Chemical lesioning of noradrenergic neurons mimicked the effects of alpha(2)-adrenoceptor blockade. Under conditions of alpha(2)-adrenoceptor blockade, the dopamine D(2) receptor-induced decrease in DARPP-32 phosphorylation was attenuated. Our data demonstrate that beta(1)- and alpha(2)-adrenoceptors regulate DARPP-32 phosphorylation in neostriatal neurons. G(i) activation by alpha(2)-adrenoceptors antagonizes G(s)/PKA signaling mediated by D(1) and A(2A) receptors in striatonigral and striatopallidal neurons, respectively, and thereby enhances D(2) receptor/G(i) signaling in striatopallidal neurons. alpha(2)-Adrenoceptors may therefore be a therapeutic target for the treatment of Parkinson's disease.

Indexed as

Adrenergic alpha-2 Receptor AntagonistsAnimalsCatalytic DomainCyclic AMP Response Element-Binding ProteinDopamineDopamine and cAMP-Regulated Phosphoprotein 32GTP-Binding Protein alpha Subunits, Gi-GoMaleMiceMice, Inbred C57BLNeostriatumNeuronsOrgan Culture TechniquesParkinson DiseasePhosphorylationReceptor, Adenosine A2AAdrenergic alpha-2 Receptor AntagonistsCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinDopamineDopamine and cAMP-Regulated Phosphoprotein 32GTP-Binding Protein alpha Subunits, Gi-GoPpp1r1b protein, mouseReceptor, Adenosine A2AReceptors, AdrenergicReceptors, Adrenergic, alpha-2Receptors, Adrenergic, beta-1Receptors, Dopamine D2Threonine

Identifiers

PMID20236221
PMCPMC2861145
OpenAlexW2022199598

What OpenQuestion holds

Textmetadata
LicenceTDM
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.