Evidence map›Paper›PMID 19217879›Full record

ArticleBiophysical journal2009

Cardiac myocyte excitation by ultrashort high-field pulses.

Sufen Wang, Jiexiao Chen, Meng-Tse Chen, P Thomas Vernier, Martin A Gundersen, Miguel Valderrábano

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 79 citations in OpenAlex.

  1. Precise mimicry of physiological CaBioengineering & translational medicine · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Excitation and electroporation by MHz bursts of nanosecond stimuli.Biochemical and biophysical research communications · 2019
    Article
  18. Article
  19. Ultrashort nanosecond electric pulses evoke heterogeneous patterns of CaBiochimica et biophysica acta. Biomembranes · 2019
    Article
  20. Excitation of murine cardiac myocytes by nanosecond pulsed electric field.Journal of cardiovascular electrophysiology · 2019
    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

6 authors at 3 institutions in 1 country.

Sufen WangDivision of Cardiac Electrophysiology, Department of Cardiology, The Methodist Hospital, Houston, Texas, USA.
Jiexiao Chen
Meng-Tse Chen
P Thomas Vernier
Martin A Gundersen
Miguel Valderrábano
University of Southern California · USMethodist Hospital · USHouston Methodist · US

Funding

Nanosecond megavolt pulse technology for cardiac stimulation and defibrillationR21HL085215 · NHLBI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI VALDERRABANO, MIGUEL · 2006 to 2007
$448k
NHLBI NIH HHS R21 HL085215NHLBI NIH HHS R21HL085215
6 · The paper itself

Abstract

In unexcitable, noncardiac cells, ultrashort (nanosecond) high-voltage (megavolt-per-meter) pulsed electrical fields (nsPEF) can mobilize intracellular Ca2+ and create transient nanopores in the plasmalemma. We studied Ca2+ responses to nsPEF in cardiac cells. Fluorescent Ca2+ or voltage signals were recorded from isolated adult rat ventricular myocytes deposited in an electrode microchamber and stimulated with conventional pulses (CPs; 0.5-2.4 kV/cm, 1 ms) or nsPEF (10-80 kV/cm, 4 ns). nsPEF induced Ca2+ transients in 68/104 cells. Repeating nsPEF increased the likelihood of Ca2+ transient induction (61.8% for <10 nsPEF vs. 80.6% for > or =10 nsPEF). Repetitive Ca2+ waves arising at the anodal side and Ca2+ destabilization occurred after repeated nsPEF (12/29) or during steady-state single nsPEF delivery at 2 Hz. Removing extracellular Ca2+ abolished responses to nsPEF. Verapamil did not affect nsPEF-induced Ca2+ transients, but decreased responses to CP. Tetrodotoxin and KB-R7943 increased the repetition threshold in response to nsPEF: 1-20 nsPEF caused local anodal Ca2+ waves without Ca2+ transients, and > or =20 nsPEF caused normal transients. Ryanodine-thapsigargin and caffeine protected against nsPEF-induced Ca2+ waves and showed less recovery of diastolic Ca2+ levels than CP. Voltage recordings demonstrated action potentials triggered by nsPEF, even in the presence of tetrodotoxin. nsPEF can mobilize intracellular Ca2+ in cardiac myocytes by inducing action potentials. Anodal Ca2+ waves and resistance to Na+ and Ca2+ channel blockade suggest nonselective ion channel transport via sarcolemmal nanopores as a triggering mechanism.

Indexed as

AnimalsCaffeineCalciumCalcium Channel BlockersCalcium SignalingCells, CulturedElectric StimulationExtracellular SpaceMembrane PotentialsMyocytes, CardiacRatsRats, Sprague-DawleyRyanodineSodium Channel BlockersTetrodotoxinThapsigargin2-(2-(4-(4-nitrobenzyloxy)phenyl)ethyl)isothiourea methanesulfonateCaffeineCalciumCalcium Channel BlockersRyanodineSodium Channel BlockersTetrodotoxinThapsigarginThioureaVerapamil

Identifiers

PMID19217879
PMCPMC2717245
OpenAlexW2005743052

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.