Evidence map›Paper›PMID 11606650›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2001

A dopamine- and protein kinase A-dependent mechanism for network adaptation in retinal ganglion cells.

C F Vaquero, A Pignatelli, G J Partida, A T Ishida

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2001. 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
1.3field-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

31 citing papers in PubMed, 63 citations in OpenAlex.

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  13. Fixation strategies for retinal immunohistochemistry.Progress in retinal and eye research · 2015
    Review
  14. Article
  15. Article
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  19. Article
  20. Dopaminergic modulation of ganglion-cell photoreceptors in rat.The European journal of neuroscience · 2012
    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

4 authors at 1 institution in 1 country.

C F VaqueroSection of Neurobiology, Physiology, and Behavior, University of California, Davis, California 95616, USA.
A Pignatelli
G J Partida
A T Ishida
University of California, Davis · US

Funding

Transgenic Mouse and Biobank CoreP01CA095616 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BRENNAN, CAMERON · 2003 to 2012
$20.3M
VISION RESEARCH CORE GRANTP30EY012576 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI Thomas M. Glaser · 1999 to 2026
$18.9M
PHARMACOLOGY &PHYSIOLOGY OF RETINAL GANGLION CELLSR01EY008120 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI ISHIDA, ANDREW T · 1995 to 2017
$6.7M
PHARMACOLOGY AND PHYSIOLOGY OF RETINAL GANGLION CELLSR29EY008120 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI ISHIDA, ANDREW T · 1989 to 1993
–
NCI NIH HHS P01 CA095616NEI NIH HHS EY08120NEI NIH HHS P30 EY012576NEI NIH HHS P30 EY12576NEI NIH HHS R01 EY008120
6 · The paper itself

Abstract

Vertebrates can detect light intensity changes in vastly different photic environments, in part, because postreceptoral neurons undergo "network adaptation." Previous data implicated dopaminergic, cAMP-dependent inhibition of retinal ganglion cells in this process yet left unclear how this occurs and whether this occurs in darkness versus light. To test for light- and dopamine-dependent changes in ganglion cell cAMP levels in situ, we immunostained dark- and light-adapted retinas with anti-cAMP antisera in the presence and absence of various dopamine receptor ligands. To test for direct effects of dopamine receptor ligands and membrane-permeable protein kinase ligands on ganglion cell excitability, we recorded spikes from isolated ganglion cells in perforated-patch whole-cell mode before and during application of these agents by microperfusion. Our immunostainings show that light, endogenous dopamine, and exogenous dopamine elevate ganglion cell cAMP levels in situ by activating D1-type dopamine receptors. Our spike recordings show that D1-type agonists and 8-bromo cAMP reduce spike frequency and curtail sustained spike firing and that these effects entail protein kinase A activation. These effects resemble those of background light on ganglion cell responses to light flashes. Network adaptation could thus be produced, to some extent, by dopaminergic modulation of ganglion cell spike generation, a mechanism distinct from modulation of transmitter release onto ganglion cells or of transmitter-gated currents in ganglion cells. Combining these observations with results obtained in studies of photoreceptor, bipolar, and horizontal cells indicates that all three layers of neurons in the retina are equipped with mechanisms for adaptation to ambient light intensity.

Indexed as

8-Bromo Cyclic Adenosine MonophosphateAction PotentialsAdaptation, OcularAnimalsCalcium Channel BlockersCell SeparationCyclic AMPCyclic AMP-Dependent Protein KinasesDarknessDichlororibofuranosylbenzimidazoleDopamineDopamine AgonistsDopamine AntagonistsGoldfishIn Vitro TechniquesLight5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole-3',5'-monophosphorothioate8-Bromo Cyclic Adenosine MonophosphateCalcium Channel BlockersCyclic AMPCyclic AMP-Dependent Protein KinasesDichlororibofuranosylbenzimidazoleDopamineDopamine AgonistsDopamine AntagonistsReceptors, Dopamine D1Thionucleotides

Identifiers

PMID11606650
PMCPMC3245881
OpenAlexW1676323133

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.