Evidence map›Paper›PMID 42265526›Full record

ReviewNeuroscience bulletin2026

Targeting Spinal Dorsal Horn Sensitisation in Chronic Pain: Mechanisms and Translational Strategies.

Volodymyr Krotov, Olga Kopach

Abstract readReview
In one paragraph

Review in Neuroscience bulletin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Volodymyr KrotovBogomoletz Institute of Physiology, Kyiv, 01024, Ukraine. vkrotov@biph.kiev.ua.ORCID http://orcid.org/0000-0001-5737-3252
Olga KopachCity St. George's University of London, London, SW17 0RE, UK. o.kopach@ucl.ac.uk.ORCID http://orcid.org/0000-0002-3921-3674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic pain is a multidimensional, highly debilitating disease arising from diverse functional and structural impairments across the nervous system. Despite heterogeneous aetiologies, chronic pain states converge on shared pathophysiological mechanisms: peripheral and central sensitisation. These dysfunctions reflect long-term functional and structural plasticity within the peripheral and central nociceptive pathways, resulting in amplified signal transmission and pain chronification. Historically, research and drug development prioritised peripheral targets to suppress nociceptive inputs, often neglecting central sensitisation, a core mechanism of treatment-resistant pain. Sensitisation of dorsal horn (DH) circuits underlies network hyperexcitability associated with disrupted excitation-inhibition balance, synaptic potentiation, and circuit reorganisation. This review summarises recent advances in delineating synaptic, cellular, and DH network-level adaptations underlying chronic pain. We discuss emerging mechanism-based strategies to restore circuit balance by targeting cell-type-specific maladaptive plasticity rather than globally suppressing neural activity. Targeted approaches hold promise for improving the specificity, efficacy, and safety of next-generation chronic pain therapies.

Indexed as

Central Nervous System SensitizationChronic PainSpinal Cord Dorsal HornAnimalsHumansNeuronal PlasticityPosterior Horn CellsCentral sensitisationChronic painDorsal horn neuronsGene therapyMaladaptive plasticityNociceptive transmissionSpinal cordSynaptic excitation and inhibition

Identifiers

PMID42265526
PMCPMC13642862

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.