| Project/Area Number |
15591266
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Radiation science
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| Research Institution | Mie University |
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Principal Investigator |
MAEDA Masayuki Mie University, School of Medicine, Assistant Professor, 医学部附属病院, 講師 (70219278)
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| Co-Investigator(Kenkyū-buntansha) |
SAKUMA Hajime Mie University, School of Medicine, Associated Professor, 医学部附属病院, 助教授 (60205797)
KAN Takeda Mie University, School of Medicine, Professor, 大学院医学系研究科, 教授 (70106988)
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| Project Period (FY) |
2003 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2006: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2005: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2004: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2003: ¥1,400,000 (Direct Cost: ¥1,400,000)
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| Keywords | Cerebral Ischemia / Hyperglycemia / Free radical inhibitor / Diffusion-weighted MRI / 脳虚血 / 拡散MRI |
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| Research Abstract |
In this study, we investigated the effect of administration time of N-nitro-L-arginine methyl ester (L-NAME), an NO-synthase inhibitor, in hyperglycemic rats of transient focal cerebral ischemia (1 h occlusion of the middle cerebral artery and reperfusion). Rats received single intraperitoneal administration of L-NAME 3 mg/kg, given immediately, 30 min, or 1 h after ischemia onset. The ischemic volume of the brain was measured using diffusion-weighted MRI (b=2000 s/mm^2) at 2h, 6 h, and 24 h after ischemia. L-NAME reduced the infarct volume by 32% at 2 h (p< 0.05), 21% at 6 h (p<0.05), and 12% at 24 h (p>0.05) compared to placebo (saline) administration when given immediately after ischemia, but it had no neuroprotective activity when given 30 min and 1 h after ischemia. L-NAME might be neuroprotective in a hyperglycemic model of transient ischemia
when given immediately after ischemia.
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