Evidence map›Paper›PMID 26621212›Full record

ArticleScientific reports2015

Optogenetics-enabled assessment of viral gene and cell therapy for restoration of cardiac excitability.

Christina M Ambrosi, Patrick M Boyle, Kay Chen, Natalia A Trayanova, Emilia Entcheva

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Cardiac optogenetics: shining light on signaling pathways.Pflugers Archiv : European journal of physiology · 2023
    Review
  3. Cardiac optogenetics: a decade of enlightenment.Nature reviews. Cardiology · 2021
    Review
  4. Article
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  9. Syncytium cell growth increases Kir2.1 contribution in human iPSC-cardiomyocytes.American journal of physiology. Heart and circulatory physiology · 2020
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Cardiac Optogenetics: 2018.JACC. Clinical electrophysiology · 2018
    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

5 authors at 2 institutions in 1 country.

Christina M AmbrosiDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, NY.
Patrick M BoyleInstitute for Computational Medicine and Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD.
Kay ChenDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, NY.
Natalia A TrayanovaInstitute for Computational Medicine and Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD.
Emilia EntchevaDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, NY.
Stony Brook University · USJohns Hopkins University · US

Funding

Virtual Electrophysiology LaboratoryDP1HL123271 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI TRAYANOVA, NATALIA A. · 2013 to 2017
$4.0M
THE BIOCHEMISTRY AND CELL BIOLOGY OF METABOLIC DISEASEST32DK007521 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI MALBON, CRAIG C · 1987 to 2012
$3.9M
Redox Modification of the Arrhythmic Substrate in Heart FailureR01HL105216 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI O'ROURKE, BRIAN, TRAYANOVA, NATALIA A. · 2011 to 2014
$3.0M
Cardiac Optogenetics: A Cell Delivery ApproachR01HL111649 · NHLBI · STATE UNIVERSITY NEW YORK STONY BROOK · PI ENTCHEVA, EMILIA · 2012 to 2016
$2.4M
Resynchronizing the Failing Heart: Insights from a Multiscale Cardiac ModelR01HL103428 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI TRAYANOVA, NATALIA A. · 2011 to 2014
$2.3M
NCCDPHP CDC HHS DP1 HL123271NHLBI NIH HHS DP1 HL123271NHLBI NIH HHS R01 HL103428NHLBI NIH HHS R01 HL105216NHLBI NIH HHS R01 HL111649NIDDK NIH HHS T32 DK007521NIDDK NIH HHS T32-DK07521
6 · The paper itself

Abstract

Multiple cardiac pathologies are accompanied by loss of tissue excitability, which leads to a range of heart rhythm disorders (arrhythmias). In addition to electronic device therapy (i.e. implantable pacemakers and cardioverter/defibrillators), biological approaches have recently been explored to restore pacemaking ability and to correct conduction slowing in the heart by delivering excitatory ion channels or ion channel agonists. Using optogenetics as a tool to selectively interrogate only cells transduced to produce an exogenous excitatory ion current, we experimentally and computationally quantify the efficiency of such biological approaches in rescuing cardiac excitability as a function of the mode of application (viral gene delivery or cell delivery) and the geometry of the transduced region (focal or spatially-distributed). We demonstrate that for each configuration (delivery mode and spatial pattern), the optical energy needed to excite can be used to predict therapeutic efficiency of excitability restoration. Taken directly, these results can help guide optogenetic interventions for light-based control of cardiac excitation. More generally, our findings can help optimize gene therapy for restoration of cardiac excitability.

Indexed as

AdenoviridaeHeart DiseasesAnimalsGenetic TherapyOptogeneticsRatsTransduction, Genetic

Identifiers

PMID26621212
PMCPMC4664892
OpenAlexW2303032511

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.