Evidence map›Paper›PMID 41457102›Full record

ArticleScientific reports2025

Optogenetic stimulation attenuates central post-stroke pain via BDNF/TrkB signaling pathway modulation in the ascending pain modulation system.

Ya-Juan Gu, Jing Chang, Fei Deng, Chao Deng

Abstract read
In one paragraph

Article in Scientific reports, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ya-Juan Gu *Department of Obstetrics, First Affiliated Hospital, Shihezi University, Shihezi, China.
Jing Chang *Department of Obstetrics, First Affiliated Hospital, Shihezi University, Shihezi, China.
Fei DengDepartment of Rehabilitation, Geriatric Rehabilitation Hospital, Urumqi City, China.
Chao DengDepartment of Anesthesiology, First Affiliated Hospital, Shihezi University, Shihezi, China. 1452793572@qq.com.

Funding

Young and Middle-aged Medical Talent Program TSYC202401B194
6 · The paper itself

Abstract

To investigate the role of BDNF/TrkB signaling in Central Post-Stroke Pain (CPSP) and to investigate whether this signaling is related to the analgesic effect of optogenetics. This study was conducted in two parts. First, 40 rats were acquired and randomly divided into four groups: Sham, CPSP, CPSP + ANA-12 (inhibitor of the BDNF/TrkB signaling pathway), and CPSP + 1% DMSO. The Sham group received a saline injection into the Ventral Posterolateral Nucleus of the Thalamus (VPL), whereas the other three groups were injected with type IV collagenase. Additionally, the two groups of CPSP rats were separately injected with ANA-12 or 1% DMSO in the VPL. Second, 50 rats were acquired and randomly divided into five groups: Sham, CPSP, CPSP + NpHR, CPSP + NpHR + BDNF, and CPSP + NpHR + PBS. From day 3 after collagenase injection, rats in the three NpHR groups received yellow laser stimulation at a wavelength of 589 nm six times a day for 12 consecutive days. Subsequently, two groups of stimulated rats were separately injected with BDNF or PBS in the VPL. Optogenetic therapy effectiveness and potential mechanisms were evaluated using pain threshold tests and molecular biology, among other methods. According to the pain threshold test results, optogenetic therapy and ANA-12 injection reversed aberrant CPSP while downregulating BDNF and TrkB. Conversely, exogenous BDNF injection reversed the therapeutic effect of optogenetics on pain. The BDNF/TrkB signaling pathway in the ascending pain modulation system may crucially modulate CPSP in rats. Furthermore, optogenetic therapy could suppress BDNF/TrkB signaling in the ascending pain modulation system, potentially alleviating thalamic hemorrhage-induced Neuropathic Pain (NP).

Indexed as

Brain-Derived Neurotrophic FactorPainReceptor, trkBStrokeAnimalsAzepinesBenzamidesMalePain ManagementRandom AllocationRatsRats, Sprague-DawleySignal TransductionANA 12 compoundAzepinesBdnf protein, ratBenzamidesBrain-Derived Neurotrophic FactorNtrk2 protein, ratReceptor, trkBBDNF/TrkBCentral post-stroke painOptogenetic techniquesPrimary motor cortexVentral posterior lateral nucleus of the thalamus

Identifiers

PMID41457102
PMCPMC12855997

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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.