| Project/Area Number |
23791945
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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 |
Otorhinolaryngology
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| Research Institution | St. Marianna University School of Medicine |
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Principal Investigator |
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| Project Period (FY) |
2011 – 2013
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| Project Status |
Completed (Fiscal Year 2013)
|
| Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Keywords | 前庭代償 / プロテオミクス / Nsf / 翻訳後修飾 / ニトロシル化修飾 / リン酸化修飾 / ニトロシル化 / リン酸化 / 小脳片葉 |
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| Research Abstract |
Unilateral labyrinthectomy (UL) in rats is used as a human vertigo model. In this model, spontaneous nystagmus and dysequilibrium caused by UL are ameliorated within 48-72 hours. This amelioration, named vestibular compensation (VC), is long lasting. Although cerebellar flocculi have been reported to be involved in VC, the molecular mechanism behind VC is still unknown. Here, we used 2D-DIGE to depict protein changes in flocculi that contribute to acute (48 hours) and chronic (1 week) stages of VC. As a result, we found that 99 out of 967 protein spots showed significant changes in their intensities. Using MALDI-TOF MS, we successfully identified 10 proteins, such as N-ethylmaleimide-sensitive fusion protein (Nsf). Among these, a possibility that posttranslational modification was participating in the acute stage of VC was suggested, and NSF was able to consider that phosphorylation of the posttranslational modification was carried out.
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