| Project/Area Number |
11694143
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Bioorganic chemistry
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| Research Institution | Gifu University |
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Principal Investigator |
SUZUKI Masaaki Gifu Univ., Faculty of Engineering, Professor, 工学部, 教授 (90093046)
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| Co-Investigator(Kenkyū-buntansha) |
HOSOYA Takamitsu Gifu Univ., Faculty of Engineering, Research Assistant, 工学部, 助手 (60273124)
WATANABE Yasuyoshi Osaka City Univ., Graduate School of Medicine, Professor, 大学院・医学研究科, 教授 (40144399)
NOYORI Ryoji Nagoya Univ., Graduate School of Science, Professor, 大学院・理学研究科, 教授 (50022554)
MATSUMURA Kiyashi Kyoto Univ., Graduate School of Informatics, Assistant Professor, 大学院・情報学研究科, 助教授 (10157349)
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| Project Period (FY) |
1999 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥12,300,000 (Direct Cost: ¥12,300,000)
Fiscal Year 2001: ¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 2000: ¥4,100,000 (Direct Cost: ¥4,100,000)
Fiscal Year 1999: ¥5,900,000 (Direct Cost: ¥5,900,000)
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| Keywords | PET / Prostacyclin / IP_2 / 15R-TIC / 15-deoxy-TIC / apoptosis / brain / アポトーシス / IP_2 / ^<11>C[CH_3] / 光親和性標識 / 神経突起伸展促進 / PET法 / in vivo / 制癌性PG |
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| Research Abstract |
An artificial prostaglandin, 15R-MTC, selectively binds to a novel prostacyclin receptor, IP_2, expressed in the central nervous system. In order to analyze function of IP_2 receptor by positron emission tomography ( PET ), design and synthesis of PET tracers and specific molecular probes based on 15R-T1C were conducted. First, rapid methylation reaction using a coordinatively unsaturated palladium ( O ) complex was elaborated for the synthesis of PET tracers with ^<11>C-CH3. This reaction was successfully applied to the synthesis of ^<11>C-labeled 15fl-TIC methyl ester with a synthetic apparatus at Uppsala University PET Centre. Specific location of the IP_2 in the brain of a living rhesus monkey was then clearly visualized by PET using the tracer. Furthermore, stepwise operation for the rapid methylation was developed, which allowed for the highly reproducible synthesis of ^<11>C-15R-TIC methyl ester with total radioactivity of ca. 2.5 GBq. This protocol enables to supply efficient radioactive PET tracers applicable to the study of human brains with volumes ten-times those of monkeys. Biological function of 15R-TIC was also investigated. Thus the compound was found to prevent the apoptotic cell death of hippocampal neurons induced under high oxygen atmosphere or serum deprivation in vitro, and in vivo, reduce the volume of brain damage in a rat model of focal cerebral ischemia. Additionally, 15-deoxy-TIC, a structurally simplified analog of 15R-TIC, was designed and synthesized. The binding affinity of 15-deoxy-TIC to IP_2 receptor was more than ten-times that of 15R-TIC, and the apoptotic death of hippocampal neurons was completely prevented by the low dose of the compound. The methyl ester of 15-deoxy-TIC could pass through the BBB to reach the brain efficiently, and revealed strong activity for brain protection in the rat model of ischemia. The synthesis of ^<11>C-labeled 15-deoxy-TIC methyl ester was also accomplished by the stepwise methylation protocol.
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