| Project/Area Number |
14572163
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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 |
応用薬理学・医療系薬学
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| Research Institution | Kobe Gakuin University |
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Principal Investigator |
TOKUYAMA Shogo Kobe Gakuin University School of Phamacy, Clinical Phamacy, Professor, 薬学部, 教授 (70225358)
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| Project Period (FY) |
2002 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 2003: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2002: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | chronic pain / pain stimulation / morphine / tolerance / neuronal cell adhesion molecule / NCAM / PKC / 細胞内情報伝達 / κオピオイド受容体 / μオピオイド受容体 |
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| Research Abstract |
It has been reported that induction of m-opioid receptors is affected by neuronal cell adhesion molecule (NCAM) in the experiment used by P19 cell line, suggesting that morphine action might be modulated by NCAM. In the present study, involvement of NCAM in the development of tolerance to morphine analgesia was examined. The tolerance was easily developed by daily injection of 10 mg/kg morphine on mice for 5 days, as evaluated by tail-flick method. On the other hand, treatment of antisense oligodeoxynucleotides (AS-ODN) for NCAM significantly inhibited its tolerance development. Recently, desensitization of opioid receptor phosphorylated by protein kinase C (PKC) as one of the mechanisms of tolerance development has been focused. In fact, phosphorylation and expression of PKCα, one of the PKC isozymes, protein was increased in the midbrain region of morphine tolerant mice in the Western blot analysis. Furthermore, the change in PKCα protein caused by multiple treatment of morphine was also reversed by AS-ODN for NCAM. These results obtained in this study demonstrate that NCAM plays an important role in the development of tolerance to morphine mediated through the regulation of phosphorylation and expression of PKCα protein.
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