Evidence map›Paper›PMID 8394569›Full record

ArticlePflugers Archiv : European journal of physiology1993

Fast Na+ current in circular smooth muscle cells of the large intestine.

Z Xiong, N Sperelakis, A Noffsinger, C Fenoglio-Preiser

Abstract read
PubMed Publisher
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Irritable bowel syndrome patients have SCN5A channelopathies that lead to decreased NaAmerican journal of physiology. Gastrointestinal and liver physiology · 2018
    Article
  3. Modelling Human Colonic Smooth Muscle Cell Electrophysiology.Cellular and molecular bioengineering · 2017
    Article
  4. Article
  5. Ranolazine inhibits voltage-gated mechanosensitive sodium channels in human colon circular smooth muscle cells.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  6. Article
  7. Article
  8. Hydrogen sulfide is a partially redox-independent activator of the human jejunum Na+ channel, Nav1.5.American journal of physiology. Gastrointestinal and liver physiology · 2011
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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.

Z XiongDepartment of Physiology and Biophysics, University of Cincinnati College of Medicine, OH 45267-0576.
N Sperelakis
A Noffsinger
C Fenoglio-Preiser
University of Cincinnati Medical Center · US

Funding

REGULATION OF ION CHANNELS IN VASCULAR SMOOTH MUSCLER01HL040572 · NHLBI · UNIVERSITY OF CINCINNATI · PI SPERELAKIS, NICHOLAS · 1990 to 1997
–
NHLBI NIH HHS HL 40572
6 · The paper itself

Abstract

Whole-cell voltage clamp was carried out on freshly dispersed single smooth muscle cells from adult rat and human colons to investigate the regulation of the Ca2+ channels. In this study, we unexpectedly discovered the existence of a fast Na+ channel current. With normal physiological salt solution (PSS) plus 4-amino-pyridine (3 mM) in the bath and high-Cs+ solution in the pipette to inhibit outward K+ currents, an inward current possessing fast and slow components was observed when the cell membrane was depolarized to a value more positive than -20 mV from a holding potential of -100 mV. When Ca2+ ions were removed from the PSS, or when nifedipine (10 microM) and Ni2+ (30 microM) were simultaneously applied, the slow component disappeared and the fast component remained. The fast current component became almost completely inactivated within 10 ms. This fast component was dependent on extracellular Na+ concentration and was inhibited by tetrodotoxin (TTX) dose dependently (IC50 of 130 nM in rat and 14 nM in human). These results suggest that the slow component of inward current was a Ca2+ channel current, whereas the fast component was a TTX-sensitive fast Na+ channel current. The threshold voltage, the voltage for peak current, and the reversal potential for the fast Na+ current were, respectively, about -50, -20, and +50 mV in rats, and -40, 0, and +60 mV in humans. The incidence of cells possessing fast Na+ currents depended on the region of the colon.(ABSTRACT TRUNCATED AT 250 WORDS)

Indexed as

AnimalsCalciumCalcium ChannelsCell MembraneCholineColonElectrophysiologyHumansIn Vitro TechniquesManganeseMuscle, SmoothNickelNifedipineRatsRats, Sprague-DawleySodiumCalciumCalcium ChannelsCholineManganeseNickelNifedipineSodiumSodium ChannelsTetrodotoxin

Identifiers

PMID8394569
OpenAlexW2019463600

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.