Evidence map›Paper›PMID 22277752›Full record

ReviewAmerican journal of physiology. Cell physiology2012

ENaCs and ASICs as therapeutic targets.

Yawar J Qadri, Arun K Rooj, Catherine M Fuller

Abstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Sensory Innervation of the Larynx and the Search for Mucosal Mechanoreceptors.Journal of speech, language, and hearing research : JSLHR · 2021
    Article
  6. Article
  7. Article
  8. A NaThe Journal of biological chemistry · 2019
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Extraoral Taste Receptor Discovery: New Light on Ayurvedic Pharmacology.Evidence-based complementary and alternative medicine : eCAM · 2017
    Review
  17. Amiloride Analogs as ASIC1a Inhibitors.CNS neuroscience & therapeutics · 2016
    Article
  18. Article
  19. Article
  20. Review
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 at 1 institution in 1 country.

Yawar J QadriDepartment of Physiology and Biophysics, University of Alabama at Birmingham, AL 35294, USA.
Arun K Rooj
Catherine M Fuller
University of Alabama at Birmingham · US

Funding

SODIUM ENTRY INTO AMILORIDE-SENSITIVE EPITHELIAR01DK037206 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FULLER, CATHERINE M · 1986 to 2014
$3.9M
NIDDK NIH HHS R01 DK037206PHS HHS 37206
6 · The paper itself

Abstract

The epithelial Na(+) channel (ENaC) and acid-sensitive ion channel (ASIC) branches of the ENaC/degenerin superfamily of cation channels have drawn increasing attention as potential therapeutic targets in a variety of diseases and conditions. Originally thought to be solely expressed in fluid absorptive epithelia and in neurons, it has become apparent that members of this family exhibit nearly ubiquitous expression. Therapeutic opportunities range from hypertension, due to the role of ENaC in maintaining whole body salt and water homeostasis, to anxiety disorders and pain associated with ASIC activity. As a physiologist intrigued by the fundamental mechanics of salt and water transport, it was natural that Dale Benos, to whom this series of reviews is dedicated, should have been at the forefront of research into the amiloride-sensitive sodium channel. The cloning of ENaC and subsequently the ASIC channels has revealed a far wider role for this channel family than was previously imagined. In this review, we will discuss the known and potential roles of ENaC and ASIC subunits in the wide variety of pathologies in which these channels have been implicated. Some of these, such as the role of ENaC in Liddle's syndrome are well established, others less so; however, all are related in that the fundamental defect is due to inappropriate channel activity.

Indexed as

Epithelial Sodium Channel AgonistsEpithelial Sodium Channel BlockersSodium Channel AgonistsAcid Sensing Ion ChannelsAnimalsCystic FibrosisEpithelial Sodium ChannelsHumansHypertensionMolecular Targeted TherapyNerve Tissue ProteinsSodium ChannelsAcid Sensing Ion ChannelsEpithelial Sodium Channel AgonistsEpithelial Sodium Channel BlockersEpithelial Sodium ChannelsNerve Tissue ProteinsSodium Channel AgonistsSodium Channels

Identifiers

PMID22277752
PMCPMC3330738
OpenAlexW2167396539

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.