Molecular mechanisms for the development of morphine tolerance.
| Project/Area Number |
20390413
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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 |
Anesthesiology/Resuscitation studies
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| Research Institution | Chiba University |
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Principal Investigator |
AOE Tomohiko Chiba University, 大学院・医学研究院, 准教授 (90311612)
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| Project Period (FY) |
2008 – 2010
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| Project Status |
Completed (Fiscal Year 2010)
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| Budget Amount *help |
¥19,630,000 (Direct Cost: ¥15,100,000、Indirect Cost: ¥4,530,000)
Fiscal Year 2010: ¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2009: ¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2008: ¥10,270,000 (Direct Cost: ¥7,900,000、Indirect Cost: ¥2,370,000)
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| Keywords | 小胞体 / シャペロン / ストレス / 疾患 / マウス / オピオイド / 耐姓 / muオピオイド受容体 / オピオイド耐性 |
|---|
| Research Abstract |
Morphine is a potent analgesic, but the molecular mechanism for tolerance formation after repeated use is not fully understood. Binding immunoglobulin protein (BiP) is an endoplasmic reticulum (ER) chaperone that is central to ER function. We examined knock-in mice expressing a mutant BiP with the retrieval sequence deleted in order to elucidate physiological processes that are sensitive to BiP functions.
Repeated morphine administration caused the development of morphine tolerance in the wild-type mice. The activation of glycogen synthase kinase 3beta (GSK-3beta) was associated with morphine tolerance, because an inhibitor of GSK-3beta prevented it. On the other hand, the mutant BiP mice showed less morphine tolerance, and the activation of GSK-3beta was suppressed in their brain. These results suggest that BiP may play an important role in the development of morphine tolerance.
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Report
(4 results)
Research Products
(32 results)
