| Project/Area Number |
24791593
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Anesthesiology/Resuscitation studies
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| Research Institution | Shimane University |
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Principal Investigator |
ISHIDA RYOSUKE 島根大学, 医学部, 特別協力研究員 (50508934)
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| Research Collaborator |
TSUMORI Toshiko 県立広島大学, 保健福祉学部, 教授 (30217377)
TAKAHASHI Mai 島根大学, 医学部, 技術職員
KATSUBE Yukiko 島根大学, 医学部, 事務補佐員
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| Project Period (FY) |
2012-04-01 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
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| Keywords | μオピオイド受容体 / 内在化 / Gタンパク質共役受容体 / オピオイド耐性 / オピオイド受容体 / 電子顕微鏡 |
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| Outline of Final Research Achievements |
Both fentanyl and DAMGO induced rapid receptor endocytosis into endosome, after just 5 min of exposure. Receptor recycling to cell membrane was almost complete within 60 min after fentanyl exposure; however, 60 min after DAMGO exposure, approximately 30% of MOR immunoreactivity was detected in the endosome, indicating slower recycling. In the early stage of internalization (5 min of exposure), MOR immunoreactivity was detected adjacent to coated vesicles near the cell membrane. In the late phase (15 and 30 min of exposures), MOR immunoreactivity was observed near lysosomes and multivesicular bodies as well as in Golgi cisterns and sacs, indicating possible degradation and de novo synthesis of MORs.
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