Evidence map›Paper›PMID 11124974›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2000

D2 dopamine receptors in striatal medium spiny neurons reduce L-type Ca2+ currents and excitability via a novel PLC[beta]1-IP3-calcineurin-signaling cascade.

S Hernandez-Lopez, T Tkatch, E Perez-Garci, E Galarraga, J Bargas, H Hamm, D J Surmeier

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 231 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
231citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

231 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  19. Amyloid-β Causes NMDA Receptor Dysfunction and Dendritic Spine Loss through mGluR1 and AKAP150-Anchored Calcineurin Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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171 more citing papers are in PubMed but not listed here.

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.

S Hernandez-LopezDepartment of Physiology and Institute for Neuroscience, Northwestern University Medical School, Chicago, Illinois 60611, USA.
T Tkatch
E Perez-Garci
E Galarraga
J Bargas
H Hamm
D J Surmeier

Funding

DOPAMINERGIC AND MUSCARINIC SIGNALING IN THE STRIATUMR37NS034696 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DALTON JAMES SURMEIER · 2001 to 2026
$7.3M
Dopaminergic and Muscarinic Signaling in the StriatumR01NS034696 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SURMEIER, DALTON JAMES · 1996 to 2018
$4.3M
G PROTEIN STRUCTURE/FUNCTIONR01EY010291 · NEI · VANDERBILT UNIVERSITY · PI HAMM, HEIDI E · 1994 to 2010
$3.9M
DOPAMINERGIC SIGNALING IN THE NUCLEUS ACCUMBENSR01DA012958 · NIDA · NORTHWESTERN UNIVERSITY · PI SURMEIER, DALTON JAMES · 2000 to 2004
$1.3M
FIC NIH HHS TW 01214NEI NIH HHS R01 EY010291NIDA NIH HHS DA 12958NIDA NIH HHS R01 DA012958NINDS NIH HHS NS 34696NINDS NIH HHS R01 NS034696NINDS NIH HHS R37 NS034696
6 · The paper itself

Abstract

In spite of the recognition that striatal D(2) receptors are critical determinants in a variety of psychomotor disorders, the cellular mechanisms by which these receptors shape neuronal activity have remained a mystery. The studies presented here reveal that D(2) receptor stimulation in enkephalin-expressing medium spiny neurons suppresses transmembrane Ca(2+) currents through L-type Ca(2+) channels, resulting in diminished excitability. This modulation is mediated by G(beta)(gamma) activation of phospholipase C, mobilization of intracellular Ca(2+) stores, and activation of the calcium-dependent phosphatase calcineurin. In addition to providing a unifying mechanism to explain the apparently divergent effects of D(2) receptors in striatal medium spiny neurons, this novel signaling linkage provides a foundation for understanding how this pivotal receptor shapes striatal excitability and gene expression.

Indexed as

Action PotentialsAdenylyl Cyclase InhibitorsAnimalsBariumCalcineurinCalcineurin InhibitorsCalciumCalcium Channel AgonistsCalcium Channel BlockersCalcium Channels, L-TypeCorpus StriatumDopamineDopamine AgonistsDopamine AntagonistsDopamine D2 Receptor AntagonistsDose-Response Relationship, DrugAdenylyl Cyclase InhibitorsBariumCalcineurinCalcineurin InhibitorsCalciumCalcium Channel AgonistsCalcium Channel BlockersCalcium Channels, L-TypeDopamineDopamine AgonistsDopamine AntagonistsDopamine D2 Receptor AntagonistsEnzyme InhibitorsInositol 1,4,5-TrisphosphateIsoenzymesPhospholipase C betaReceptors, Dopamine D2SulpirideType C Phospholipases

Identifiers

PMID11124974
PMCPMC6773013

What OpenQuestion holds

Textmetadata
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.