Evidence map›Paper›PMID 31437161›Full record

ArticlePLoS computational biology2019

A computational model for gonadotropin releasing cells in the teleost fish medaka.

Geir Halnes, Simen Tennøe, Trude M Haug, Gaute T Einevoll, Finn-Arne Weltzien, Kjetil Hodne

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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 2 institutions in 1 country.

Geir HalnesFaculty for Science and Technology, Norwegian University of Life Sciences, Ås, Norway.ORCID 0000-0002-4721-1599
Simen TennøeCentre for Integrative Neuroplasticity, University of Oslo, Oslo, Norway.ORCID 0000-0002-0120-8992
Trude M HaugInstitute of Oral Biology, University of Oslo, Oslo, Norway.ORCID 0000-0003-3776-5077
Gaute T EinevollFaculty for Science and Technology, Norwegian University of Life Sciences, Ås, Norway.ORCID 0000-0002-5425-5012
Finn-Arne WeltzienDepartment of Basic Sciences and Aquatic Medicine, Norwegian University of Life Sciences, Campus Adamstuen, Oslo, Norway.ORCID 0000-0002-5111-1558
Kjetil HodneDepartment of Basic Sciences and Aquatic Medicine, Norwegian University of Life Sciences, Campus Adamstuen, Oslo, Norway.ORCID 0000-0001-8528-9728
University of Oslo · NONorwegian University of Life Sciences · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pituitary endocrine cells fire action potentials (APs) to regulate their cytosolic Ca2+ concentration and hormone secretion rate. Depending on animal species, cell type, and biological conditions, pituitary APs are generated either by TTX-sensitive Na+ currents (INa), high-voltage activated Ca2+ currents (ICa), or by a combination of the two. Previous computational models of pituitary cells have mainly been based on data from rats, where INa is largely inactivated at the resting potential, and spontaneous APs are predominantly mediated by ICa. Unlike in rats, spontaneous INa-mediated APs are consistently seen in pituitary cells of several other animal species, including several species of fish. In the current work we develop a computational model of gonadotropin releasing cells in the teleost fish medaka (Oryzias latipes). The model stands out from previous modeling efforts by being (1) the first model of a pituitary cell in teleosts, (2) the first pituitary cell model that fires sponateous APs that are predominantly mediated by INa, and (3) the first pituitary cell model where the kinetics of the depolarizing currents, INa and ICa, are directly fitted to voltage-clamp data. We explore the firing properties of the model, and compare it to the properties of previous models that fire ICa-based APs. We put a particular focus on how the big conductance K+ current (IBK) modulates the AP shape. Interestingly, we find that IBK can prolong AP duration in models that fire ICa-based APs, while it consistently shortens the duration of the predominantly INa-mediated APs in the medaka gonadotroph model. Although the model is constrained to experimental data from gonadotroph cells in medaka, it may likely provide insights also into other pituitary cell types that fire INa-mediated APs.

Indexed as

Models, BiologicalAction PotentialsAnimalsCalciumComputational BiologyComputer SimulationFemaleFish ProteinsGonadotrophsGonadotropins, PituitaryIon ChannelsKineticsLarge-Conductance Calcium-Activated Potassium ChannelsOryziasCalciumFish ProteinsGonadotropins, PituitaryIon ChannelsLarge-Conductance Calcium-Activated Potassium Channels

Identifiers

PMID31437161
PMCPMC6726249
OpenAlexW2969653066

What Socratic 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 Socratic graph.