Evidence map›Paper›PMID 27605532›Full record

ArticleJournal of neurophysiology2016

Dynamic balance of excitation and inhibition rapidly modulates spike probability and precision in feed-forward hippocampal circuits.

Sarah Wahlstrom-Helgren, Vitaly A Klyachko

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Channelopathies in fragile X syndrome.Nature reviews. Neuroscience · 2021
    Review
  3. Hyperexcitability and Homeostasis in Fragile X Syndrome.Frontiers in molecular neuroscience · 2021
    Article
  4. Article
  5. 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

2 authors.

Sarah Wahlstrom-HelgrenDepartments of Cell Biology & Physiology and Biomedical Engineering, Center for the Investigation of Membrane Excitable Diseases, Washington University School of Medicine, St. Louis, Missouri.
Vitaly A KlyachkoDepartments of Cell Biology & Physiology and Biomedical Engineering, Center for the Investigation of Membrane Excitable Diseases, Washington University School of Medicine, St. Louis, Missouri klyachko@wustl.edu.

Funding

MULTIPLE ROLES OF FMRP IN SYNAPTIC FUNCTION AND PLASTICITYR01NS081972 · NINDS · WASHINGTON UNIVERSITY · PI KLYACHKO, VITALY A · 2012 to 2016
$1.7M
NINDS NIH HHS R01 NS081972
6 · The paper itself

Abstract

Feed-forward inhibitory (FFI) circuits are important for many information-processing functions. FFI circuit operations critically depend on the balance and timing between the excitatory and inhibitory components, which undergo rapid dynamic changes during neural activity due to short-term plasticity (STP) of both components. How dynamic changes in excitation/inhibition (E/I) balance during spike trains influence FFI circuit operations remains poorly understood. In the current study we examined the role of STP in the FFI circuit functions in the mouse hippocampus. Using a coincidence detection paradigm with simultaneous activation of two Schaffer collateral inputs, we found that the spiking probability in the target CA1 neuron was increased while spike precision concomitantly decreased during high-frequency bursts compared with a single spike. Blocking inhibitory synaptic transmission revealed that dynamics of inhibition predominately modulates the spike precision but not the changes in spiking probability, whereas the latter is modulated by the dynamics of excitation. Further analyses combining whole cell recordings and simulations of the FFI circuit suggested that dynamics of the inhibitory circuit component may influence spiking behavior during bursts by broadening the width of excitatory postsynaptic responses and that the strength of this modulation depends on the basal E/I ratio. We verified these predictions using a mouse model of fragile X syndrome, which has an elevated E/I ratio, and found a strongly reduced modulation of postsynaptic response width during bursts. Our results suggest that changes in the dynamics of excitatory and inhibitory circuit components due to STP play important yet distinct roles in modulating the properties of FFI circuits.

Indexed as

Action PotentialsAnimalsElectric StimulationExcitatory Amino Acid AntagonistsFemaleFragile X Messenger Ribonucleoprotein 1HippocampusIn Vitro TechniquesMaleMiceMice, Inbred C57BLMice, TransgenicModels, NeurologicalNerve NetNeural InhibitionNeurons2-amino-5-phosphopentanoic acidExcitatory Amino Acid AntagonistsFG 9041Fmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1QuinoxalinesValinefeed-forward inhibitionshort-term plasticitysynaptic dynamics

Identifiers

PMID27605532
PMCPMC5133295

What OpenQuestion holds

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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.