The regulation of immune response by haloperidol via the effects on the redox equibrium in dendritic cells
| Project/Area Number |
25462433
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Anesthesiology
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| Research Institution | Osaka University |
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Principal Investigator |
Kashiwa Yozo 大阪大学, 医学(系)研究科(研究院), 助教 (90647471)
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| Co-Investigator(Kenkyū-buntansha) |
FUJINO YUJI 大阪大学, 大学院医学系研究科, 教授 (50252672)
OHTA NORIYUKI 大阪大学, 医学部附属病院, 助教 (60379162)
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| Project Period (FY) |
2013-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | 樹状細胞 / ハロペリドール / ドーパミン / D2様受容体 / インターロイキン12 / ドーパミンD2受容体 / 一酸化炭素 / インターロイキン６ / 接触過敏症 / T細胞 |
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| Outline of Final Research Achievements |
We analyzed the effects of haloperidol on dendritic cell (DC) and DC-mediated immune response. haloperidol suppressed the maturation of immature DCs induced by LPS. Furthermore, we analyzed the effect of haloperidol on DC-mediated immune response by the use of contact hypersensitivity model of mouse. Haloperidol-treated DC suppressed the development of contact hypersensitivity in mouse. This model is assumed to be developed by typical Th1 immune response. Out results strongly suggest that haloperidol suppress the maturation of immature DCs and the development of Th1 type immune response. In addition, the inhibitory effect was mediated by dopamine D2-like receptor via the inhibition of NF-κB in immune cells such as macrophages and DCs.
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Report
(3 results)
Research Products
(5 results)
