Evidence map›Paper›PMID 40650301›Full record

ArticleInternational journal of molecular sciences2025

Mapping Morphine's Antinociceptive Impact on the Ventral Tegmental Area During Nociceptive Stimulation: A Novel Microimaging Approach in a Neuropathic Pain Model.

Austin Ganaway, Airi Kamata, Dunyan Yao, Kazuto Sakoori, Ryoma Okada, Ting Chen, Yasumi Ohta, Jun Ohta, Masahiro Ohsawa, Metin Akay and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. An Implanted Tooth That Can Feel.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    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

11 authors.

Austin GanawayBiomedical Engineering Department, University of Houston, 3517 Cullen Blvd, Houston, TX 77204, USA.ORCID 0000-0003-1413-5742
Airi KamataLaboratory of Systems Pharmacology, Faculty of Pharmaceutical Sciences, Teikyo University, Tokyo 173-8605, Japan.
Dunyan YaoBiomedical Engineering Department, University of Houston, 3517 Cullen Blvd, Houston, TX 77204, USA.ORCID 0009-0009-8549-5068
Kazuto SakooriLaboratory of Systems Pharmacology, Faculty of Pharmaceutical Sciences, Teikyo University, Tokyo 173-8605, Japan.
Ryoma OkadaDivision of Materials Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma 630-0101, Japan.ORCID 0000-0002-3496-919X
Ting ChenBiomedical Engineering Department, University of Houston, 3517 Cullen Blvd, Houston, TX 77204, USA.
Yasumi OhtaDivision of Materials Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma 630-0101, Japan.ORCID 0000-0002-0333-4626
Jun OhtaDivision of Materials Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma 630-0101, Japan.ORCID 0000-0001-8194-9020
Masahiro OhsawaLaboratory of Systems Pharmacology, Faculty of Pharmaceutical Sciences, Teikyo University, Tokyo 173-8605, Japan.
Metin AkayBiomedical Engineering Department, University of Houston, 3517 Cullen Blvd, Houston, TX 77204, USA.ORCID 0000-0002-2988-4669
Yasemin M AkayBiomedical Engineering Department, University of Houston, 3517 Cullen Blvd, Houston, TX 77204, USA.ORCID 0000-0003-1753-6293

Funding

Fostering Joint International Research 22KK0180Japan Society for the Promotion of Science 23H05450Japan Society for the Promotion of Science 24K02786
6 · The paper itself

Abstract

The neurobiology of chronic pain is complex and multifaceted, intertwining with the mesocorticolimbic system to regulate the behavioral and perceptional response to adverse stimuli. Specifically, the ventral tegmental area (VTA), the dopaminergic hub of the reward pathways located deep within the midbrain, is crucial for regulating the release of dopamine (DA) throughout the central nervous system (CNS). To better understand the nuances among chronic pain, VTA response, and therapeutics, implementing progressive approaches for mapping and visualizing the deep brain in real time during nociceptive stimulation is crucial. In this study, we utilize a fluorescence imaging platform with a genetically encoded calcium indicator (GCaMP6s) to directly visualize activity in the VTA during acute nociceptive stimulation in both healthy adult mice and adult mice with partial nerve ligation (PNL)-induced neuropathic pain. We also investigate the visualization of the analgesic properties of morphine. Deep brain imaging using our self-fabricated µ-complementary metal-oxide-semiconductor (CMOS) imaging device allows the tracking of the VTA's response to adverse stimuli. Our findings show that nociceptive stimulation is associated with a reduction in VTA fluorescence activity, supporting the potential of this platform for visualizing pain-related responses in the central nervous system. Additionally, treatment with morphine significantly reduces the neuronal response caused by mechanical stimuli and is observable using the CMOS imaging platform, demonstrating a novel way to potentially assess and treat neuropathic pain.

Indexed as

MorphineNeuralgiaNociceptionVentral Tegmental AreaAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLMorphinechronic painCMOS imagingdopaminefluorescence imagingGABAGCaMP6morphineneuropathic painpartial nerve ligation modelVTA

Identifiers

PMID40650301
PMCPMC12250161

What OpenQuestion holds

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Registered trials

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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.