Evidence map›Paper›PMID 38829509›Full record

ArticleMolecular neurobiology2025

Ido2 Deficiency Exacerbates Motor Impairment and Reduces Aryl Hydrocarbon Receptor Activity through Decreased Kynurenine in a Chronic Demyelinating Mouse Model.

Kazuo Kunisawa, Mitsuki Hara, Koyo Yoshidomi, Yuki Kon, Yasuko Yamamoto, Suwako Fujigaki, Bolati Wulaer, Aika Kosuge, Moeka Tanabe, Sei Saitoh and 4 more

Abstract read
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Article in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

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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

2 citing papers in PubMed.

  1. Review
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4 · The record

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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

14 authors.

Kazuo KunisawaDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan. kunisawa@fujita-hu.ac.jp.
Mitsuki HaraDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan.
Koyo YoshidomiDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan.
Yuki KonDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan.
Yasuko YamamotoDepartment of Advanced Diagnostic System Development, Fujita Health University Graduate School of Health Sciences, Aichi, Japan.
Suwako FujigakiDepartment of Advanced Diagnostic System Development, Fujita Health University Graduate School of Health Sciences, Aichi, Japan.
Bolati WulaerDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan.
Aika KosugeDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan.
Moeka TanabeDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan.
Sei SaitohDepartment of Biomedical Molecular Sciences, Fujita Health University School of Medicine, Aichi, Japan.
Kazuo TakahashiDepartment of Biomedical Molecular Sciences, Fujita Health University School of Medicine, Aichi, Japan.
Kuniaki SaitoDepartment of Advanced Diagnostic System Development, Fujita Health University Graduate School of Health Sciences, Aichi, Japan.
Toshitaka NabeshimaLaboratory of Health and Medical Science Innovation, Fujita Health University Graduate School of Health Science, Aichi, Japan.
Akihiro MouriDepartment of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University Graduate School of Health Science, Aichi, 470-1192, Japan. mouri@fujita-hu.ac.jp.

Funding

Japan Science and Technology Agency JPMJFR215HJapan Society for the Promotion of Science 20K07931Japan Society for the Promotion of Science 22J15573Japan Society for the Promotion of Science 22K07606Japan Society for the Promotion of Science 22K11891Japan Society for the Promotion of Science 23H02843
6 · The paper itself

Abstract

Demyelinating diseases including multiple sclerosis (MS) are chronic inflammatory diseases of the central nervous system. Indoleamine 2,3-dioxygenase 2 (Ido2) is a recently identified as catalytic enzyme involved in the rate-limiting step of the tryptophan-kynurenine pathway that influences susceptibility to inflammatory diseases. However, the pathological role of Ido2 in demyelination remains unclear. In this study, we investigated whether Ido2 deficiency influences the pathogenesis of proteolipid protein transgenic (Plp tg) mice, an animal model of chronic demyelination. Ido2 deficiency exacerbates impairments of motor function in the locomotor activity test, wire hanging test, and rotarod test. Ido2 deficiency caused severe demyelination associated with CD68-positive microglial activation in Plp tg mice. In the cerebellum of Plp tg mice, Ido2 deficiency significantly increased the expression of Tnfα. Ido2 deficiency reduced tryptophan metabolite kynurenine (KYN) levels and subsequent aryl hydrocarbon receptor (AhR) activity, which play an important role in anti-inflammatory response. These results suggest that Ido2 has an important role in preventing demyelination through AhR. Taken together, Ido2 could be a potential therapeutic target for demyelinating diseases.

Indexed as

Demyelinating DiseasesDisease Models, AnimalIndoleamine-Pyrrole 2,3,-DioxygenaseKynurenineReceptors, Aryl HydrocarbonAnimalsChronic DiseaseMiceMice, Inbred C57BLMice, TransgenicMicrogliaMotor ActivityMotor DisordersIDO2 protein, mouseIndoleamine-Pyrrole 2,3,-DioxygenaseKynurenineReceptors, Aryl HydrocarbonDemyelinationIdo2Kynurenine pathwayMicrogliaMultiple sclerosis

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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.