Evidence map›Paper›PMID 16760352›Full record

ArticleJournal of neurophysiology2006

Creation and reduction of a morphologically detailed model of a leech heart interneuron.

Anne-Elise Tobin, Stephen D Van Hooser, Ronald L Calabrese

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Neuronal morphology enhances robustness to perturbations of channel densities.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  4. Article
  5. Article
  6. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Analogous synaptic plasticity profiles emerge from disparate channel combinations.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  12. Development of modified cable models to simulate accurate neuronal active behaviors.Journal of applied physiology (Bethesda, Md. : 1985) · 2014
    Article
  13. Article
  14. Article
  15. Article
  16. Article
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  18. Article
  19. Article
  20. Signal propagation in Drosophila central neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    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

3 authors at 1 institution in 1 country.

Anne-Elise TobinDepartment of Biology, Emory University, Atlanta, GA 30322, USA.
Stephen D Van Hooser
Ronald L Calabrese
Emory University · US

Funding

NEUROMODULATORY INFLUENCES ON MOTOR SYSTEMSR01NS024072 · NINDS · EMORY UNIVERSITY · PI CALABRESE, RONALD L · 1985 to 2011
$3.6M
Neuromodulatory Influences on Motor SystemsR56NS024072 · NINDS · EMORY UNIVERSITY · PI CALABRESE, RONALD L · 2013 to 2013
$386k
Neuromodulation of a Rhythmic NetworkF31NS042983 · NINDS · EMORY UNIVERSITY · PI TOBIN, ANNE-ELISE · 2002 to 2004
$76k
NINDS NIH HHS F31 NS042983NINDS NIH HHS NS-24072NINDS NIH HHS NS-42983NINDS NIH HHS R01 NS024072NINDS NIH HHS R56 NS024072
6 · The paper itself

Abstract

Conductance-based neuron models aid in understanding the role intrinsic and synaptic currents play in producing neuronal activity. Incorporating morphological detail into a model allows for additional analysis of nonhomogeneous distributions of active and synaptic conductances, as well as spatial segregation of electrical events. We developed a morphologically detailed "Full Model" of a leech heart interneuron that replicates reasonably well intracellular recordings from these interneurons. However, it constitutes hundreds of compartments, each increasing parameter space and simulation time. To reduce the number of compartments of the Full Model, while preserving conductance densities and distributions, its compartments were grouped into functional groups that each share identical conductance densities. Each functional group was sequentially reduced to one or two compartments, preserving surface area, conductance densities, and its contribution to input resistance. As a result, the input resistance and membrane time constant were preserved. The axial resistances of several compartments were rescaled to match the amplitude of synaptic currents and low-threshold calcium currents and the shape of action potentials to those in the Full Model. This reduced model, with intrinsic conductances, matched the activity of the Full Model for a variety of simulated current-clamp and voltage-clamp data. Because surface area and conductance distribution of the functional groups of the Full Model were maintained, parameter changes introduced into the reduced model can be directly translated to the Full Model. Thus our computationally efficient reduced morphology model can be used as a tool for exploring the parameter space of the Full Model and in network simulations.

Indexed as

Models, BiologicalModels, TheoreticalAction PotentialsAnimalsCalcium ChannelsElectrophysiologyHeartInterneuronsLeechesNeural ConductionPatch-Clamp TechniquesSynapsesCalcium Channels

Identifiers

PMID16760352
PMCPMC2897741
OpenAlexW2097105955

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.