Evidence map›Paper›PMID 31152125›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

Is Optogenetic Activation of Vglut1-Positive Aβ Low-Threshold Mechanoreceptors Sufficient to Induce Tactile Allodynia in Mice after Nerve Injury?

Alexander Chamessian, Megumi Matsuda, Michael Young, Michelle Wang, Zhi-Jun Zhang, Di Liu, Brielle Tobin, Zhen-Zhong Xu, Thomas Van de Ven, Ru-Rong Ji

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Spinal Processing of Spatiotemporally Diverse Tactile Stimuli: Computational Insights into Allodynia and Spinal Cord Stimulation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. Gene therapy for chronic pain management.Cell reports. Medicine · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 2 institutions in 2 countries.

Alexander ChamessianDepartment of Anesthesiology, alexander.chamessian@duke.edu.ORCID 0000-0002-7775-2062
Megumi MatsudaDepartment of Anesthesiology.
Michael YoungDepartment of Neurobiology, and.
Michelle WangDepartment of Anesthesiology.
Zhi-Jun ZhangDepartment of Anesthesiology.ORCID 0000-0001-6996-8683
Di LiuDepartment of Anesthesiology.
Brielle TobinDepartment of Anesthesiology.
Zhen-Zhong XuDepartment of Anesthesiology.
Thomas Van de VenDepartment of Anesthesiology.
Ru-Rong JiDepartment of Anesthesiology.
Institute of Neurobiology · BGDuke University · US

Funding

Neuronal and glial interactions of neuropathic painR01DE017794 · NIDCR · DUKE UNIVERSITY · PI BUCHHEIT, THOMAS · 2006 to 2021
$6.6M
Resolution pathway of painR01NS087988 · NINDS · DUKE UNIVERSITY · PI JI, RU-RONG · 2014 to 2018
$1.7M
NIDCR NIH HHS R01 DE017794NINDS NIH HHS R01 NS087988
6 · The paper itself

Abstract

Mechanical allodynia is a cardinal feature of pathological pain. Recent work has demonstrated the necessity of Aβ-low-threshold mechanoreceptors (Aβ-LTMRs) for mechanical allodynia-like behaviors in mice, but it remains unclear whether these neurons are sufficient to produce pain under pathological conditions. We generated a transgenic mouse in which channelrhodopsin-2 (ChR2) is conditionally expressed in vesicular glutamate transporter 1 (Vglut1) sensory neurons (Vglut1-ChR2), which is a heterogeneous population of large-sized sensory neurons with features consistent with Aβ-LTMRs. In naive male Vglut1-ChR2 mice, transdermal hindpaw photostimulation evoked withdrawal behaviors in an intensity- and frequency-dependent manner, which were abolished by local anesthetic and selective A-fiber blockade. Surprisingly, male Vglut1-ChR2 mice did not show significant differences in light-evoked behaviors or real-time aversion after nerve injury despite marked hypersensitivity to punctate mechanical stimuli. We conclude that optogenetic activation of cutaneous Vglut1-ChR2 neurons alone is not sufficient to produce pain-like behaviors in neuropathic mice.

Indexed as

AnimalsFemaleHyperalgesiaMaleMechanoreceptorsMiceMice, TransgenicNeuralgiaOptogeneticsPeripheral Nerve InjuriesSensory Receptor CellsVesicular Glutamate Transport Protein 1Vesicular Glutamate Transport Protein 1allodynianeuropathicoptogeneticspain

Identifiers

PMID31152125
PMCPMC6668198
OpenAlexW2947551934

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.