Evidence map›Paper›PMID 22773861›Full record

ArticleJournal of the mechanics and physics of solids2012

Computational Optogenetics: A Novel Continuum Framework for the Photoelectrochemistry of Living Systems.

Jonathan Wong, Oscar J Abilez, Ellen Kuhl

Abstract read
In one paragraph

Article in Journal of the mechanics and physics of solids, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Cardiac optogenetics: a decade of enlightenment.Nature reviews. Cardiology · 2021
    Review
  3. Review
  4. Predicting the cardiac toxicity of drugs using a novel multiscale exposure-response simulator.Computer methods in biomechanics and biomedical engineering · 2018
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Cardiac applications of optogenetics.Progress in biophysics and molecular biology · 2014
    Review
  12. Review
  13. Article
  14. Generating fibre orientation maps in human heart models using Poisson interpolation.Computer methods in biomechanics and biomedical engineering · 2014
    Article
  15. Computational modeling of chemo-electro-mechanical coupling: a novel implicit monolithic finite element approach.International journal for numerical methods in biomedical engineering · 2013
    Article
  16. Article
  17. Advances in modeling ventricular arrhythmias: from mechanisms to the clinic.Wiley interdisciplinary reviews. Systems biology and medicine
    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.

Jonathan WongDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA, jonjwong@stanford.edu.
Oscar J Abilez
Ellen Kuhl
Stanford University · US

Funding

Physics-based Simulation of Biological Structures(RMI)U54GM072970 · NIGMS · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2004 to 2013
$33.5M
Predoctoral Training Bioinformatics/Computational Biol.T32GM063495 · NIGMS · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2001 to 2009
$1.7M
NIGMS NIH HHS T32 GM063495NIGMS NIH HHS U54 GM072970
6 · The paper itself

Abstract

Electrical stimulation is currently the gold standard treatment for heart rhythm disorders. However, electrical pacing is associated with technical limitations and unavoidable potential complications. Recent developments now enable the stimulation of mammalian cells with light using a novel technology known as optogenetics. The optical stimulation of genetically engineered cells has significantly changed our understanding of electrically excitable tissues, paving the way towards controlling heart rhythm disorders by means of photostimulation. Controlling these disorders, in turn, restores coordinated force generation to avoid sudden cardiac death. Here, we report a novel continuum framework for the photoelectrochemistry of living systems that allows us to decipher the mechanisms by which this technology regulates the electrical and mechanical function of the heart. Using a modular multiscale approach, we introduce a non-selective cation channel, channelrhodopsin-2, into a conventional cardiac muscle cell model via an additional photocurrent governed by a light-sensitive gating variable. Upon optical stimulation, this channel opens and allows sodium ions to enter the cell, inducing electrical activation. In side-by-side comparisons with conventional heart muscle cells, we show that photostimulation directly increases the sodium concentration, which indirectly decreases the potassium concentration in the cell, while all other characteristics of the cell remain virtually unchanged. We integrate our model cells into a continuum model for excitable tissue using a nonlinear parabolic second order partial differential equation, which we discretize in time using finite differences and in space using finite elements. To illustrate the potential of this computational model, we virtually inject our photosensitive cells into different locations of a human heart, and explore its activation sequences upon photostimulation. Our computational optogenetics tool box allows us to virtually probe landscapes of process parameters, and to identify optimal photostimulation sequences with the goal to pace human hearts with light and, ultimately, to restore mechanical function.

Identifiers

PMID22773861
PMCPMC3388516
OpenAlexW2140332303

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.