2021 Fiscal Year Final Research Report
Development of atopic dermatitis evaluation method using biometrically measured reactive oxygen species (ROS) as an index
Project/Area Number |
19K12758
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Review Section |
Basic Section 90110:Biomedical engineering-related
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Research Institution | Kyushu University |
Principal Investigator |
Eto Hinako 九州大学, 先端医療オープンイノベーションセンター, 特任助教 (30557632)
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Project Period (FY) |
2019-04-01 – 2022-03-31
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Keywords | DNP-MRI / ニトロキシルラジカル / ROS / レドックス / アトピ-性皮膚炎 / 窒素同位体 |
Outline of Final Research Achievements |
By analyzing the radical decay of the radical probe administered in vivo with a dynamic nuclear polarized magnetic resonance imaging (DNP-MRI) device, it was caused by reactive oxygen species(ROS) due to inflammation and the redox state (oxidation-reduction balance) causing by ROS. In this study, we established a method for simultaneous imaging analysis of two types of probes that react intracellularly or extracellularly in skin lesions of atopic dermatitis model mice. Using this method, it was possible to detect that even if the atopic dermatitis of the model mouse was visually mild such as scales (exfoliation of the stratum corneum), inflammation and thickening of the skin occurred . And,it was possible to grasp by the change in the radical decay rate of the radical probe, that the occurrence of ROS due to inflammatory cells may be the highest before the severity of the disease.
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Free Research Field |
物理系薬学
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Academic Significance and Societal Importance of the Research Achievements |
成人のアトピー性皮膚炎患者は社会的ストレスなど複雑な要因が相まって、炎症のコントロールが長期化、複雑化する。またステロイド忌避感情など慢性治療への足かせとなっている。治療継続の指標となる、『潜在的な炎症が残っている期間』を明確にする為にも、見えない皮膚炎を数値化できるバイオマーカーが必須である。本研究でのラジカルプロ-ブのラジカル減衰速度変化は、目視での軽度から中度の皮膚炎と相関した減衰速度の上昇として非侵襲に捉える事ができ、皮膚炎を数値化するバイオマ-カ-と成り得る可能性が示された。
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