Evidence map›Paper›PMID 32341097›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2020

Intracellular Calcium Responses Encode Action Potential Firing in Spinal Cord Lamina I Neurons.

Erika K Harding, Bruno Boivin, Michael W Salter

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Spike rate inference from mouse spinal cord calcium imaging data.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Excitatory and Inhibitory Neurons of the Spinal Cord Superficial Dorsal Horn Diverge in Their Somatosensory Responses and PlasticityThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  9. Article
  10. RyR-mediated CaProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Review
  12. Review
  13. 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 3 institutions in 2 countries.

Erika K HardingProgram in Neurosciences & Mental Health, The Hospital for Sick Children, Toronto, Ontario Canada M5G 0A4 michael.salter@sickkids.ca erika.harding@ucalgary.ca.
Bruno BoivinProgram in Neurosciences & Mental Health, The Hospital for Sick Children, Toronto, Ontario Canada M5G 0A4.
Michael W SalterProgram in Neurosciences & Mental Health, The Hospital for Sick Children, Toronto, Ontario Canada M5G 0A4 michael.salter@sickkids.ca erika.harding@ucalgary.ca.ORCID 0000-0001-6897-6585
Boston Children's Hospital · USUniversity of Calgary · CAUniversity of Toronto · CA

Funding

CIHR FDN-15433
6 · The paper itself

Abstract

Maladaptive plasticity of neurons in lamina I of the spinal cord is a lynchpin for the development of chronic pain, and is critically dependent on intracellular calcium signaling. However, the relationship between neuronal activity and intracellular calcium in these neurons is unknown. Here we combined two-photon calcium imaging with whole-cell electrophysiology to determine how action potential firing drives calcium responses within subcellular compartments of male rat spinal cord lamina I neurons. We found that single action potentials generated at the soma increase calcium concentration in the somatic cytosol and nucleus, and these calcium responses invade dendrites and dendritic spines by active backpropagation. Calcium responses in each compartment were dependent on voltage-gated calcium channels, and somatic and nuclear calcium responses were amplified by release of calcium from ryanodine-sensitive intracellular stores. Grouping single action potential-evoked calcium responses by neuron type demonstrated their presence in all defined types, as well as a high degree of similarity in calcium responses between neuron types. With bursts of action potentials, we found that calcium responses have the capacity to encode action potential frequency and number in all compartments, with action potential number being preferentially encoded. Together, these findings indicate that intracellular calcium serves as a readout of neuronal activity within lamina I neurons, providing a unifying mechanism through which activity may regulate plasticity, including that seen in chronic pain.

Indexed as

Action PotentialsAnimalsCalciumFemaleIntracellular FluidMaleMiceMice, Inbred C57BLNeuronsOrgan Culture TechniquesRatsRats, Sprague-DawleySpinal Cord Dorsal HornCalciumcalcium imagingdendritesdendritic spineslamina Inucleusspinal cord

Identifiers

PMID32341097
PMCPMC7275865
OpenAlexW3019169923

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.