Evidence map›Paper›PMID 40816765›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Peripheral Gating of Nociception Investigated with a Decerebrate, Arterially Perfused Preparation of the Rat.

Varinder K Lall, Pierce Mullen, Stephen W Milne, Hao Han, Xiaona Du, Nikita Gamper

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Varinder K LallFaculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom v.k.lall@leeds.ac.uk.
Pierce MullenFaculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.
Stephen W MilneFaculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.
Hao HanDepartment of Pharmacology, Hebei Medical University, Shijiazhuang 050011, China.
Xiaona DuDepartment of Pharmacology, Hebei Medical University, Shijiazhuang 050011, China.
Nikita GamperFaculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.ORCID 0000-0001-5806-0207

Funding

Wellcome Trust
6 · The paper itself

Abstract

There is growing evidence that sensory neurons within the dorsal root ganglia (DRGs) are equipped with mechanisms for "gating" nociceptive information before it enters the central nervous system. However, direct in vivo evidence remains limited due to the anatomical inaccessibility of the DRG. Here, we developed a decerebrate, arterially perfused preparation of the rat (of either sex) that allows simultaneous recordings from the C8 spinal nerve (SN) and dorsal root (DR), with full access to the corresponding DRG in the absence of anesthesia. The C8 segment contributes to the median nerve supplying the forepaw, which was used for sensory stimulation. Spikes in DR were recorded and temporally matched to their origin spikes in the SN. Noxious mechanical stimulation to the forepaw increased firing in both the SN and the DR, and application of GABA (200 µM) or the GABA reuptake inhibitor, NO-711 (200 µM), directly into the DRG significantly reduced firing frequency only in the DR without affecting SN activity. Spike sorting revealed that this reduction in the spike rate from SN to DR, a phenomenon we term here as "filtering," was greater for C-fiber spikes compared with A-fiber spikes. Innocuous stimuli (brush/cotton bud strokes and proprioceptive stimulation) also increased firing in both SN and DR, but GABA application into the DRG failed to reduce DR firing rates. Taken together, our findings lend direct support to the hypothesis of peripheral gating of the nociceptive signaling at the DRG and highlight the therapeutic potential of these peripheral structures.

Indexed as

Decerebrate StateGanglia, SpinalNociceptionAction PotentialsAnimalsFemaleMalePerfusionPhysical StimulationRatsRats, Sprague-DawleySpinal Nerve Rootsdorsal root ganglionGABAnociceptorpainperipheral gatesomatosensory system

Identifiers

PMID40816765
PMCPMC12444853

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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.