| Project/Area Number |
15K10568
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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 | University of Occupational and Environmental Health, Japan |
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Principal Investigator |
HARA Koji 産業医科大学, 大学病院, 准教授 (20331001)
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| Co-Investigator(Kenkyū-buntansha) |
原西 保典 産業医科大学, 医学部, 非常勤医師 (90449942)
佐多 竹良 産業医科大学, 名誉教授、学長等, 名誉教授 (60128030)
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| Project Period (FY) |
2015-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | 神経障害性痛 / アンギオテンシン受容体 / 中枢作用 / 鎮痛作用 / 抗不安作用 / 抗うつ作用 / 神経障害性疼痛 |
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| Outline of Final Research Achievements |
Central effects of angiotensin receptor subtypes on hyperalgesia, anxiety, and depression were examined in rat neuropathic pain models. In chronic constriction injury (CCI) model and diabetic polyneuropathy model, AT1/AT2 receptor agonist angiotensin II and a selective AT2 receptor agonist CGA42112A inhibited cold and mechanical hyperalgesia. In contrast, an AT1 receptor antagonist losartan exacerbated cold and mechanical hyperalgesia. In the CCI model, angiotensin II and CGA42112A decreased percent of the time spent in the central area and total moving distance in the open field test. They decreased time spent in the open arms in the elevated plus maze. They also decreased swimming time and increased immobility time in the forced swim test. These results indicate that AT1 and AT2 receptors in the brain modulate nociceptive transmission and are involved in anxiety and depression in the neuropathic pain models.
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