Evidence map›Paper›PMID 22171034›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Essential role for phosphatidylinositol 4,5-bisphosphate in the expression, regulation, and gating of the slow afterhyperpolarization current in the cerebral cortex.

Claudio Villalobos, Robert C Foehring, Jonathan C Lee, Rodrigo Andrade

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Targeting 5-HTNeuroscience letters · 2022
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Phosphatidylinositol 4,5-bisphosphate (PIPThe Journal of physiology · 2017
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. A sodium-pump-mediated afterhyperpolarization in pyramidal neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    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

4 authors.

Claudio VillalobosDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.
Robert C Foehring
Jonathan C Lee
Rodrigo Andrade

Funding

Slowly Inactivating K+ Channels in Pyramidal NeuronsR01NS044163 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI FOEHRING, ROBERT C, SPAIN, WILLIAM J · 2003 to 2022
$6.5M
MECHANISMS AND REGULATION OF 5HT RECEPTORS IN THE CNSR01MH043985 · NIMH · WAYNE STATE UNIVERSITY · PI ANDRADE, RODRIGO · 1993 to 2017
$5.7M
MECHANISMS AND REGULATION OF 5-HT RECEPTORS IN THE CNSR29MH043985 · NIMH · SAINT LOUIS UNIVERSITY · PI ANDRADE, RODRIGO · 1988 to 1992
–
NIMH NIH HHS MH43985NIMH NIH HHS R01 MH043985NIMH NIH HHS R29 MH043985NINDS NIH HHS NS044163NINDS NIH HHS R01 NS044163
6 · The paper itself

Abstract

Many neurons of the CNS and peripheral nervous system express a slow afterhyperpolarization that is mediated by a slow calcium-activated potassium current. Previous work has shown that this aftercurrent regulates repetitive firing and is an important target for neuromodulators signaling through receptors coupled to G-proteins of the Gα(q-11) and Gα(s) subtypes. Yet, despite considerable effort, a molecular-level understanding of the potassium current underlying the slow afterhyperpolarization and its modulation has proven elusive. Here, we use a combination of pharmacological and molecular biological approaches in cortical brain slices to show that the functional expression of the slow calcium-activated afterhyperpolarizing current in pyramidal cells is critically dependent on membrane phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P(2)] and that this dependence accounts for its inhibition by 5-HT(2A) receptors. Furthermore, we show that PtdIns(4,5)P(2) regulates the calcium sensitivity of I(sAHP) in a manner that suggests it acts downstream from the rise in intracellular calcium. These results clarify key functional aspects of the slow afterhyperpolarization current and its modulation by 5-HT(2A) receptors and point to a key role for PtdIns(4,5)P(2) in the gating of this current.

Indexed as

AnimalsCalciumCerebral CortexMaleMembrane PotentialsMicePatch-Clamp TechniquesPhosphatidylinositol 4,5-DiphosphatePotassiumPyramidal CellsRatsRats, Sprague-DawleyReceptor, Serotonin, 5-HT2ACalciumPhosphatidylinositol 4,5-DiphosphatePotassiumReceptor, Serotonin, 5-HT2A

Identifiers

PMID22171034
PMCPMC3263352

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.