| Project/Area Number |
01870098
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| Research Category |
Grant-in-Aid for Developmental Scientific Research
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| Allocation Type | Single-year Grants |
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| Research Field |
Biological pharmacy
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| Research Institution | Hokkaido University |
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Principal Investigator |
NOMURA Yasuyuki Hokkaido University・Fac. Pharmac. Sci. ・Professor, 薬学部, 教授 (00034041)
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| Co-Investigator(Kenkyū-buntansha) |
TOHDA Michihisa Hokkaido Univ. ・Fac. Pharmac. Sci. ・Assistant, 薬学部, 教務職員 (20207525)
KITAMURA Yoshihisa Hokkaido Univ. ・Fac. Pharmac. Sci. ・Assistant, 薬学部, 助手 (60195295)
TOKUMITU Yukiko Hokkaido Univ. ・Fac. Pharmac. Sci. ・Assistant professor, 薬学部, 助教授 (60001046)
TOMIMORI Tuyoshi Hokuriku Univ. ・School of Pharmacy・Professor, 薬学部, 教授 (30100506)
KIKUCHI Tohru Toyama Med. and Pharm. Univ. ・Inst. for WAKAN-YAKU・Professor, 和漢薬研究所, 教授 (40025680)
村山 俊彦 北海道大学, 薬学部, 助手 (90174317)
上田 亨 北海道大学, 薬学部, 教授 (00001032)
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| Project Period (FY) |
1989 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥12,900,000 (Direct Cost: ¥12,900,000)
Fiscal Year 1991: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 1990: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 1989: ¥7,700,000 (Direct Cost: ¥7,700,000)
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| Keywords | Senile dementia / Nootropic / Screening methods / alpha_2-receptor / Glutamate-receptor / Oriental medicines / Senescent accelerated mice / Second messengers / 神経細胞 / アデノシン受容体 / cyclic AMP |
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| Research Abstract |
We have been investigated the involvement of the second messenger systems in memory function in the brain. We found novel adenosine analogs strongly and selectively acting on adenosine receptors and flavonoids purified from oriental harbs acting on alpha_2-receptors. In this year, we studied on pharmacological actions of flavonoids, specially of eupafolin which most strongly inhibited the adenylate cyclase in NG108-15 cells. Eupafolin inhibited adenylate cyclase activity in both NG108-15 cells and primary cultured neurons form rat hipocampus, although it did not influence inositol phosphates formation and the cGMP content in NG108-15 and arachidonic acid release in cultured neurons. Administration of eupafolin into mice (i. p.) induced sedation and inhibition of spontaneous locomoter activities. These effects were blocked by yohimbine. Eupafolin also prolonged thiopental-induced loss of righting reflex. Furthermore, eupafolin selectively inhibited the high affinity binding site of [ ^3H]clonidine in rat brain synaptic membranes. These results suggest that eupafolin selectively stimulated alpha_2-receptors. Scince clonidine, and alpha_2-receptor agonist, has been shown to ameliorate memory function, eupafolin could be expected as a nootropic drug.
We also found abnormal age-related changes in 1) the content and release of glutamic acid, 2) NMDA-receptor/ion channels and 3) protein kinase C in senescence accelerated mice (SAM), suggesting that SAM seems to be 1) an excellent animal model of accelerating aging as well as of memory disfunction and 2) useful for screening of drugs acting on brain aging and memory.
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