Evidence map›Paper›PMID 42396643›Full record

ReviewInternational journal of molecular medicine2026

TRPV1‑mediated central sensitisation: Core mechanisms of migraine chronification and novel targeted therapeutic strategies (Review).

Mingxia Zhang, Yuting Pu, Yujie Zhang, Jia Hu, Shuangyang Li, Hongmei Tang, Bangjiang Fang, Xue Bai

Abstract readReview
In one paragraph

Review in International journal of molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Mingxia Zhang *Department of Neurology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.
Yuting Pu *Department of Neurology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.
Yujie Zhang *Department of Neurology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.
Jia HuDepartment of Neurology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.
Shuangyang LiDepartment of Neurology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.
Hongmei TangDepartment of Neurology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.
Bangjiang FangCollege of Integrated Traditional and Western Medicine, Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.
Xue BaiDepartment of Neurology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646600, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Migraines are highly prevalent and disabling neurological disorders. Central sensitisation constitutes the core pathophysiological basis for its recurrent and chronic nature. Transient receptor potential vanilloid 1 (TRPV1), a key molecule in pain signalling, is not only involved in peripheral nociception, but is also highly expressed in central pain‑processing regions. TRPV1 directly contributes to the initiation and maintenance of central sensitisation, positioning it as a promising therapeutic target for migraine management. The present review systematically summarised the biological characteristics of TRPV1 and its associations with central sensitisation and migraines. The molecular mechanisms through which TRPV1 mediates central sensitisation are elaborated upon, including the regulation of neurotransmitter release, activation of glial cells, involvement in inflammatory responses and modulation of synaptic plasticity. Furthermore, the research progress and clinical challenges of TRPV1‑targeted strategies are discussed, including antagonists, agonists and genetic regulation. Lastly, the present study proposes future research directions at both basic and clinical levels, providing a novel molecular perspective on migraine pathogenesis and establishing a theoretical foundation for the development of targeted clinical therapies.

Indexed as

Central Nervous System SensitizationMigraine DisordersTRPV Cation ChannelsAnimalsHumansMolecular Targeted TherapyNeuronal PlasticitySignal TransductionTRPV1 protein, humanTRPV Cation Channelscentral sensitisationglial cellsmigraineneurotransmitterssynaptic plasticitytargeted therapytransient receptor potential vanilloid 1

Identifiers

PMID42396643
PMCPMC13354327

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.