Evidence map›Paper›PMID 30104963›Full record

ArticleFrontiers in neural circuits2018

Hyperactive Response of Direct Pathway Striatal Projection Neurons to L-dopa and D1 Agonism in Freely Moving Parkinsonian Mice.

Ben Sagot, Li Li, Fu-Ming Zhou

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neural circuits, 2018. 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
1.2field-weighted citation impact, top 22% 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, 25 citations in OpenAlex.

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  13. Evolving concepts on bradykinesia.Brain : a journal of neurology · 2020
    Review
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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

3 authors at 1 institution in 1 country.

Ben SagotDepartment of Pharmacology, College of Medicine, The University of Tennessee Health Science Center, Memphis, TN, United States.
Li LiDepartment of Pharmacology, College of Medicine, The University of Tennessee Health Science Center, Memphis, TN, United States.
Fu-Ming ZhouDepartment of Pharmacology, College of Medicine, The University of Tennessee Health Science Center, Memphis, TN, United States.
University of Tennessee Health Science Center · US

Funding

Ion channel mechanisms of striatal dopaminergic motor stimulationR01NS097671 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI ZHOU, FU-MING · 2016 to 2020
$1.7M
NINDS NIH HHS R01 NS097671
6 · The paper itself

Abstract

Dopamine (DA) profoundly stimulates motor function as demonstrated by the hypokinetic motor symptoms in Parkinson's disease (PD) and by the hyperkinetic motor side effects during dopaminergic treatment of PD. Dopamine (DA) receptor-bypassing, optogenetics- and chemogenetics-induced spike firing of striatal DA D1 receptor (D1R)-expressing, direct pathway medium spiny neurons (dSPNs or dMSNs) promotes movements. However, the endogenous D1R-mediated effects, let alone those of DA replacement, on dSPN spike activity in freely-moving animals is not established. Here we show that using transcription factor Pitx3 null mutant (Pitx3Null) mice as a model for severe and consistent DA denervation in the dorsal striatum in Parkinson's disease, antidromically identified striatonigral neurons (D1R-expressing dSPNs) had a lower baseline spike firing rate than that in DA-intact normal mice, and these neurons increased their spike firing more strongly in Pitx3Null mice than in WT mice in response to injection of L-dopa or the D1R agonist, SKF81297; the increase in spike firing temporally coincided with the motor-stimulating effects of L-dopa and SKF81297. Taken together, these results provide the first evidence from freely moving animals that in parkinsonian striatum, identified behavior-promoting dSPNs become hyperactive upon the administration of L-dopa or a D1 agonist, likely contributing to the profound dopaminergic motor stimulation in parkinsonian animals and PD patients.

Indexed as

Parkinson DiseaseAnimalsBehavior, AnimalDenervationDisease Models, AnimalDopamine AgonistsDopaminergic NeuronsHomeodomain ProteinsHyperkinesisLevodopaMiceMice, Inbred C57BLMice, TransgenicNeostriatumNeuronsReceptors, Dopamine D1Dopamine Agonistshomeobox protein PITX3Homeodomain ProteinsLevodopaReceptors, Dopamine D1Transcription Factors4-dihydroxyphenylalanine (L-dopa)antidromic stimulation collisionbasal gangliadopamine receptorL-3medium spiny neuronstriatumsubstantia nigratetrode spike recording

Identifiers

PMID30104963
PMCPMC6077202
OpenAlexW2846803016

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.