Evidence map›Paper›PMID 32847128›Full record

ArticleInternational journal of molecular sciences2020

Structural and Functional Maturation of Rat Primary Motor Cortex Layer V Neurons.

Bruno Benedetti, Dominik Dannehl, Jan Maximilian Janssen, Corinna Corcelli, Sébastien Couillard-Després, Maren Engelhardt

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Neuronal and Brain Maturation.International journal of molecular sciences · 2022
    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 2 countries.

Bruno BenedettiSpinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), 5020 Salzburg, Austria.ORCID 0000-0002-4286-5067
Dominik DannehlSpinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), 5020 Salzburg, Austria.
Jan Maximilian JanssenInstitute of Neuroanatomy, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.
Corinna CorcelliInstitute of Neuroanatomy, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.
Sébastien Couillard-DesprésSpinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), 5020 Salzburg, Austria.ORCID 0000-0002-8486-6412
Maren EngelhardtInstitute of Neuroanatomy, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.
Heidelberg University · DEParacelsus Medical University · AT

Funding

Austrian Agency for International Cooperation in Education and Research (OeAD-GmbH) HR02/2018Deutsche Forschungsgemeinschaft SFB 1134German National Academic Foundation 00Medical Faculty Mannheim MD FellowshipParacelsus Medical University Research Support Fund (PMU-FFF) R-16/04/084-BEN and R-20/02/130-BEN
6 · The paper itself

Abstract

Rodent neocortical neurons undergo prominent postnatal development and maturation. The process is associated with structural and functional maturation of the axon initial segment (AIS), the site of action potential initiation. In this regard, cell size and optimal AIS length are interconnected. In sensory cortices, developmental onset of sensory input and consequent changes in network activity cause phasic AIS plasticity that can also control functional output. In non-sensory cortices, network input driving phasic events should be less prominent. We, therefore, explored the relationship between postnatal functional maturation and AIS maturation in principal neurons of the primary motor cortex layer V (M1LV), a non-sensory area of the rat brain. We hypothesized that a rather continuous process of AIS maturation and elongation would reflect cell growth, accompanied by progressive refinement of functional output properties. We found that, in the first two postnatal weeks, cell growth prompted substantial decline of neuronal input resistance, such that older neurons needed larger input current to reach rheobase and fire action potentials. In the same period, we observed the most prominent AIS elongation and significant maturation of functional output properties. Alternating phases of AIS plasticity did not occur, and changes in functional output properties were largely justified by AIS elongation. From the third postnatal week up to five months of age, cell growth, AIS elongation, and functional output maturation were marginal. Thus, AIS maturation in M1LV is a continuous process that attunes the functional output of pyramidal neurons and associates with early postnatal development to counterbalance increasing electrical leakage due to cell growth.

Indexed as

Action PotentialsAge FactorsAnimalsAxon Initial SegmentCell DifferentiationCells, CulturedGrowthModels, NeurologicalMotor CortexMotor NeuronsNeurogenesisNeuronal PlasticityRatsaxon initial segment (AIS)developmentmaturationmotor cortexmotor neuronspatch clamp

Identifiers

PMID32847128
PMCPMC7503395
OpenAlexW3080167904

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.