Evidence map›Paper›PMID 25974163›Full record

ArticlePain2015

Electrical stimulation of low-threshold afferent fibers induces a prolonged synaptic depression in lamina II dorsal horn neurons to high-threshold afferent inputs in mice.

Andrei D Sdrulla, Qian Xu, Shao-Qiu He, Vinod Tiwari, Fei Yang, Chen Zhang, Bin Shu, Ronen Shechter, Srinivasa N Raja, Yun Wang and 2 more

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Pain, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 9% 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.

NCT04475133 nacompletednot on this mapstarted 2020, after this paper: background citation

Effects of Percutaneous Neuromodulation on Plasticity in the Somatosensory System

TypeinterventionalSponsorClinica Francisco Ortega Rehabilitacion Avanzada SLRan2020 to 2020Enrolled29ConditionsHealthyArmsUltrasound guided percutaneous neuromodulation
NCT05390359 nacompletednot on this mapstarted 2022, after this paper: background citation

Characterization of the Effects on Bioimpedance and the Sensorimotor System After the Application of Percutaneous Electrolysis Protocols on the Patellar Tendon.

TypeinterventionalSponsorClinica Francisco Ortega Rehabilitacion Avanzada SLRan2022 to 2023Enrolled50ConditionsHealthyArmsHigh-intensity and short-duration, Low-intensity and long-duration, High-intensity, short-duration and 20 Hz, Sham electrolysis
3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Electrophysiologic Characteristics of Epidural Spinal Signals in Preclinical Models of Spinal Cord Stimulation.Neuromodulation : journal of the International Neuromodulation Society · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Peripheral and central pathogenesis of postherpetic neuralgia.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Review
  14. Review
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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

12 authors at 4 institutions in 2 countries.

Andrei D SdrullaDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD, USA The Solomon H. Snyder Department of Neuroscience, Center for Sensory Biology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA Howard Hughes Medical Institute, Johns Hopkins University, School of Medicine, Baltimore, MD, USA Department of Anesthesiology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Qian Xu
Shao-Qiu He
Vinod Tiwari
Fei Yang
Chen Zhang
Bin Shu
Ronen Shechter
Srinivasa N Raja
Yun Wang
Xinzhong Dong
Yun Guan
Johns Hopkins University · USJohns Hopkins Medicine · USCapital Medical University · CNHoward Hughes Medical Institute · US

Funding

INJURY-INDUCES PAIN-- CHEMICAL MODULATION OF NOCICEPTORSR01NS026363 · NINDS · JOHNS HOPKINS UNIVERSITY · PI RAJA, SRINIVASA N. · 1989 to 2021
$6.8M
Functional analysis of the Mrg receptor family in pain sensationR01NS054791 · NINDS · JOHNS HOPKINS UNIVERSITY · PI DONG, XINZHONG · 2007 to 2020
$5.0M
Mrgs as New Target for the Treatment of Neuropathic PainR01NS070814 · NINDS · JOHNS HOPKINS UNIVERSITY · PI GUAN, YUN · 2011 to 2020
$3.2M
Functional Analysis of Mrgpr Family in itch sensationR37NS054791 · NINDS · JOHNS HOPKINS UNIVERSITY · PI Xinzhong Dong · 2022 to 2026
$2.9M
Howard Hughes Medical InstituteNINDS NIH HHS NS26363NINDS NIH HHS NS54791NINDS NIH HHS NS70814NINDS NIH HHS R01 NS026363NINDS NIH HHS R01 NS054791NINDS NIH HHS R01 NS070814NINDS NIH HHS R37 NS054791
6 · The paper itself

Abstract

Electrical stimulation of low-threshold Aβ-fibers (Aβ-ES) is used clinically to treat neuropathic pain conditions that are refractory to pharmacotherapy. However, it is unclear how Aβ-ES modulates synaptic responses to high-threshold afferent inputs (C-, Aδ-fibers) in superficial dorsal horn. Substantia gelatinosa (SG) (lamina II) neurons are important for relaying and modulating converging spinal nociceptive inputs. We recorded C-fiber-evoked excitatory postsynaptic currents (eEPSCs) in spinal cord slices in response to paired-pulse test stimulation (500 μA, 0.1 millisecond, 400 milliseconds apart). We showed that 50-Hz and 1000-Hz, but not 4-Hz, Aβ-ES (10 μA, 0.1 millisecond, 5 minutes) induced prolonged inhibition of C-fiber eEPSCs in SG neurons in naive mice. Furthermore, 50-Hz Aβ-ES inhibited both monosynaptic and polysynaptic forms of C-fiber eEPSC in naive mice and mice that had undergone spinal nerve ligation (SNL). The paired-pulse ratio (amplitude second eEPSC/first eEPSC) increased only in naive mice after 50-Hz Aβ-ES, suggesting that Aβ-ES may inhibit SG neurons by different mechanisms under naive and nerve-injured conditions. Finally, 50-Hz Aβ-ES inhibited both glutamatergic excitatory and GABAergic inhibitory interneurons, which were identified by fluorescence in vGlut2-Td and glutamic acid decarboxylase-green fluorescent protein transgenic mice after SNL. These findings show that activities in Aβ-fibers lead to frequency-dependent depression of synaptic transmission in SG neurons in response to peripheral noxious inputs. However, 50-Hz Aβ-ES failed to induce cell-type-selective inhibition in SG neurons. The physiologic implication of this novel form of synaptic depression for pain modulation by Aβ-ES warrants further investigation.

Indexed as

Action PotentialsAnimalsBicucullineDisease Models, AnimalElectric StimulationExcitatory Amino Acid AgentsGABA-A Receptor AntagonistsGlutamate DecarboxylaseGlycine AgentsGreen Fluorescent ProteinsLong-Term Synaptic DepressionLuminescent ProteinsMiceMice, Inbred C57BLMice, TransgenicNerve FibersBicucullineExcitatory Amino Acid AgentsGABA-A Receptor AntagonistsGlutamate DecarboxylaseGlycine AgentsGreen Fluorescent ProteinsLuminescent ProteinsRed Fluorescent ProteinSlc17a6 protein, mouseVesicular Glutamate Transport Protein 2

Identifiers

PMID25974163
PMCPMC4437220
OpenAlexW2056547337

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.