Evidence map›Paper›PMID 20519576›Full record

ArticleJournal of neurophysiology2010

Cell specific dopamine modulation of the transient potassium current in the pyloric network by the canonical D1 receptor signal transduction cascade.

Hongmei Zhang, Edmund W Rodgers, Wulf-Dieter C Krenz, Merry C Clark, Deborah J Baro

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2010. 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 24% 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, 26 citations in OpenAlex.

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  11. Review
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  13. Tonic dopamine induces persistent changes in the transient potassium current through translational regulation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
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  15. Article
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

5 authors at 1 institution in 1 country.

Hongmei ZhangDepartment of Biology, Georgia State University, Atlanta, Georgia 30302-4010, USA.
Edmund W Rodgers
Wulf-Dieter C Krenz
Merry C Clark
Deborah J Baro
Georgia State University · US

Funding

Mechanisms underlying opposing neuronal responses to brief vs. prolonged dopamineR01DA024039 · NIDA · GEORGIA STATE UNIVERSITY · PI BARO, DEBORAH JEAN · 2008 to 2012
$1.7M
NIDA NIH HHS DA024039NIDA NIH HHS R01 DA024039
6 · The paper itself

Abstract

Dopamine (DA) modifies the motor pattern generated by the pyloric network in the stomatogastric ganglion (STG) of the spiny lobster, Panulirus interruptus, by directly acting on each of the circuit neurons. The 14 pyloric neurons fall into six cell types, and DA actions are cell type specific. The transient potassium current mediated by shal channels (I(A)) is a common target of DA modulation in most cell types. DA shifts the voltage dependence of I(A) in opposing directions in pyloric dilator (PD) versus lateral pyloric (LP) neurons. The mechanism(s) underpinning cell-type specific DA modulation of I(A) is unknown. DA receptors (DARs) can be classified as type 1 (D1R) or type 2 (D2R). D1Rs and D2Rs are known to increase and decrease intracellular cAMP concentrations, respectively. We hypothesized that the opposing DA effects on PD and LP I(A) were due to differences in DAR expression patterns. In the present study, we found that LP expressed somatodendritic D1Rs that were concentrated near synapses but did not express D2Rs. Consistently, DA modulation of LP I(A) was mediated by a Gs-adenylyl cyclase-cAMP-protein kinase A pathway. Additionally, we defined antagonists for lobster D1Rs (flupenthixol) and D2Rs (metoclopramide) in a heterologous expression system and showed that DA modulation of LP I(A) was blocked by flupenthixol but not by metoclopramide. We previously showed that PD neurons express D2Rs, but not D1Rs, thus supporting the idea that cell specific effects of DA on I(A) are due to differences in receptor expression.

Indexed as

8-Bromo Cyclic Adenosine MonophosphateAction PotentialsAnimalsColforsinCyclic AMPDopamineDopamine AntagonistsDose-Response Relationship, DrugDrug InteractionsElectric StimulationGanglia, InvertebrateIn Vitro TechniquesIsoquinolinesNerve NetNeuronsPalinuridae8-Bromo Cyclic Adenosine MonophosphateColforsinCyclic AMPDopamineDopamine AntagonistsedelfosineIsoquinolinesN-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamidePhospholipid EthersPotassiumPotassium Channel BlockersProtein Kinase InhibitorsReceptors, Dopamine D1SulfonamidesTetraethylammoniumTetrodotoxin

Identifiers

PMID20519576
PMCPMC2934939
OpenAlexW2144891104

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.