Curriculum Vitaes
Profile Information
- Affiliation
- Professor, Department of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University School of Medical Sciences, Fujita Health University
- Degree
- 博士(薬学)
- Researcher number
- 70850551
- ORCID ID
https://orcid.org/0000-0002-2889-9586- J-GLOBAL ID
- 202001007661048523
- researchmap Member ID
- R000007329
Research Interests
5Research Areas
1Research History
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Jun, 2025 - Present
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Apr, 2016 - Present
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Oct, 2023 - May, 2025
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Jul, 2019 - Sep, 2023
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Apr, 2013 - Mar, 2016
Awards
5Papers
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Fujita medical journal, 11(3) 129-134, Aug, 2025OBJECTIVES: Sivelestat sodium hydrate (SSH) may be effective in the early stage of acute respiratory distress syndrome (ARDS) before the neutrophil extracellular trap scaffold structure is complete. Therefore, patients with suppression of fibrinolysis (SF) before the secondary fibrinolytic process might benefit from SSH administration. The primary aim of this study was to determine the effect of the SF state and combination therapy on the effect of SSH administration. METHODS: We retrospectively reviewed the data of patients diagnosed with ARDS at Fujita Health University Hospital between July 2005 and December 2016. Patients with ARDS were stratified into the SF and hyperfibrinolysis (HF) groups. Using the fibrin degradation product (FDP)/D-dimer ratio, cut-off values were set as follows: FDP/D-dimer >2 for the HF group and FDP/D-dimer ≤2 for the SF group. The 28-day mortality was the primary endpoint. RESULTS: In total, 168 patients (71 in the HF group and 97 in the SF group) were included in the analysis. The mortality within 28 days was not different based on SSH administration in either group (HF group: p=0.956, SF group: p=0.957). In the SF group, the mortality rate within 28 days in SSH-treated patients who received antithrombotic drugs was significantly higher than that in patients who received SSH only (p<0.05). However, this finding was not present in the HF group (p=0.786). CONCLUSIONS: Concomitant use of SSH and antithrombotic drugs might worsen the treatment outcome of patients with ADRS in the SF state.
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Journal of pharmaceutical health care and sciences, 11(1) 54-54, Jul 1, 2025 Lead authorCorresponding author
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In Vivo, 39(3) 1647-1653, Apr 28, 2025
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Clinical Drug Investigation, Mar 13, 2025
Misc.
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日本アルコール・薬物医学会雑誌, 45(3) 147-56, 2010A major clinical problem in treating drug abusers or addicts is the high rate of relapse to abuse even long after abstinence. In drug dependence research, drug self-administration displays excellent face validity, good construct validity, and appealing predictive validity with respect to drug consumption in humans. Because of the technical feasibility of intravenous drug self-administration, it is limited in mice relative to larger animals. Nevertheless, technical innovations made in the last 10 years have vastly improved the feasibility of long-term studies in mice. In addition, mice with targeted gene mutations, such as transgenic and knockout mice, provide a powerful tool for investigating candidate genes that may be involved in abuse of drugs in humans. Therefore, it is essential for researchers to extend the extinction-reinstatement procedure in mice. However, there are few reports that proven the relationship between genetic factor and relapsing behavior using drug self-administration procedure in mice. Based on recent documented information and our own experiences, in the present review, we described some procedural considerations for the successful establishment of drug self-administration procedure in mice, and then summarized some behavioral characteristics of genetic mouse models under the drug self-administration, and reinstatement procedure.
Professional Memberships
6Research Projects
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科学研究費助成事業, 日本学術振興会, Apr, 2023 - Mar, 2026
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臨床研究・治験推進研究事業, 日本医療研究開発機構, Apr, 2024 - Mar, 2026
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科学研究費助成事業, 日本学術振興会, Apr, 2023 - Mar, 2026
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ワクチン開発推進事業, 日本医療研究開発機構, Sep, 2020 - Mar, 2022