Evidence map›Paper›PMID 28280255›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

Dendritic GIRK Channels Gate the Integration Window, Plateau Potentials, and Induction of Synaptic Plasticity in Dorsal But Not Ventral CA1 Neurons.

Ruchi Malik, Daniel Johnston

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–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

39 citing papers in PubMed.

  1. Article
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  5. T-type CaCell reports · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Neuronal G protein-gated KAmerican journal of physiology. Cell physiology · 2022
    Review
  10. Review
  11. Article
  12. Article
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  15. Article
  16. Roles of PLCβ, PIPJournal of cellular physiology · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors.

Ruchi MalikCenter for Learning and Memory and Department of Neuroscience, University of Texas at Austin, Austin, Texas 78712 ruchi@ca1.clm.utexas.edu djohnston@mail.clm.utexas.edu.ORCID 0000-0003-0611-8790
Daniel JohnstonCenter for Learning and Memory and Department of Neuroscience, University of Texas at Austin, Austin, Texas 78712 ruchi@ca1.clm.utexas.edu djohnston@mail.clm.utexas.edu.ORCID 0000-0002-9733-1011

Funding

Cellular Information Processing in the HippocampusR01NS084473 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI JOHNSTON, DANIEL · 2013 to 2017
$1.7M
NINDS NIH HHS R01 NS084473
6 · The paper itself

Abstract

Studies comparing neuronal activity at the dorsal and ventral poles of the hippocampus have shown that the scale of spatial information increases and the precision with which space is represented declines from the dorsal to ventral end. These dorsoventral differences in neuronal output and spatial representation could arise due to differences in computations performed by dorsal and ventral CA1 neurons. In this study, we tested this hypothesis by quantifying the differences in dendritic integration and synaptic plasticity between dorsal and ventral CA1 pyramidal neurons of rat hippocampus. Using a combination of somatic and dendritic patch-clamp recordings, we show that the threshold for LTP induction is higher in dorsal CA1 neurons and that a G-protein-coupled inward-rectifying potassium channel mediated regulation of dendritic plateau potentials and dendritic excitability underlies this gating. By contrast, similar regulation of LTP is absent in ventral CA1 neurons. Additionally, we show that generation of plateau potentials and LTP induction in dorsal CA1 neurons depends on the coincident activation of Schaffer collateral and temporoammonic inputs at the distal apical dendrites. The ventral CA1 dendrites, however, can generate plateau potentials in response to temporally dispersed excitatory inputs. Overall, our results highlight the dorsoventral differences in dendritic computation that could account for the dorsoventral differences in spatial representation.

Indexed as

Action PotentialsAnimalsBarium CompoundsCA1 Region, HippocampalChloridesDendritesExcitatory Postsynaptic PotentialsG Protein-Coupled Inwardly-Rectifying Potassium ChannelsIon Channel GatingMaleNeuronal PlasticityNeuronsOrgan Culture TechniquesRatsRats, Sprague-Dawleybarium chlorideBarium CompoundsChloridesG Protein-Coupled Inwardly-Rectifying Potassium ChannelsCA1 pyramidal neuronsdorsoventral axisG-protein-coupled inward-rectifying potassium channelslong-term potentiationmembrane potentialplateau potentials

Identifiers

PMID28280255
PMCPMC5394901

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.