Evidence map›Paper›PMID 30673366›Full record

ArticleJournal of neurophysiology2019

D-type potassium channels normalize action potential firing between dorsal and ventral CA1 neurons of the mouse hippocampus.

Gregory J Ordemann, Christopher J Apgar, Darrin H Brager

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Sodium sensitivity of KJournal of neurophysiology · 2021
    Article
  9. Spatio-temporal heterogeneity in hippocampal metabolism in control and epilepsy conditions.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Article
  12. 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

3 authors.

Gregory J OrdemannDepartment of Neuroscience, Institute for Neuroscience, Center for Learning and Memory, University of Texas at Austin , Austin, Texas.
Christopher J ApgarDepartment of Neuroscience, Institute for Neuroscience, Center for Learning and Memory, University of Texas at Austin , Austin, Texas.
Darrin H BragerDepartment of Neuroscience, Institute for Neuroscience, Center for Learning and Memory, University of Texas at Austin , Austin, Texas.

Funding

PRE-DOCTORAL TRAINING IN INTERDISCIPLINARY NEUROSCIENCET32DA018926 · NIDA · UNIVERSITY OF TEXAS AUSTIN · PI Nace L Golding, AMY LEE · 2004 to 2026
$5.6M
Hippocampal channelopathies in Fragile X SyndromeR01MH100510 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI BRAGER, DARRIN H · 2015 to 2019
$1.9M
Hippocampal channelopathies in Fragile X SyndromeR56MH100510 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI BRAGER, DARRIN H · 2020 to 2020
$441k
NIDA NIH HHS T32 DA018926NIMH NIH HHS R01 MH100510NIMH NIH HHS R56 MH100510
6 · The paper itself

Abstract

Specific memory processes and neurological disorders can be ascribed to different dorsoventral regions of the hippocampus. Recently, differences in the anatomical and physiological properties between dorsal and ventral hippocampal CA1 neurons were described for both the rat and mouse hippocampus and have greatly contributed to our understanding of these processes. While differences in the subthreshold properties were similar between rat and mouse neurons, differences in action potential output between dorsal and ventral neurons were strikingly less divergent in mouse compared with rat CA1 neurons. Here, we investigate the mechanism underlying the lack of difference in action potential firing between dorsal and ventral CA1 pyramidal neurons in mouse hippocampus. Consistent with rat, we found that ventral CA1 neurons had a more depolarized resting membrane potential and higher input resistance than dorsal CA1 neurons in the mouse hippocampus. Despite these differences, action potential output in response to current injection was not significantly different. We found that ventral neurons have a more depolarized action potential threshold compared with dorsal neurons and that threshold in ventral neurons was more sensitive to block of K

Indexed as

Action PotentialsAnimalsCA1 Region, HippocampalMaleMiceMice, Inbred C57BLNeuronsShaker Superfamily of Potassium ChannelsShaker Superfamily of Potassium Channels4-APintrinsic excitabilitymorphologyoutside-out patch clamp

Identifiers

PMID30673366
PMCPMC6520617

What OpenQuestion holds

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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.