On the role of subtypes of muscarinic receptors in the inner ear
| Project/Area Number |
15591798
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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 |
Otorhinolaryngology
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| Research Institution | The University of Tokyo |
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Principal Investigator |
ITO Ken The University of Tokyo, Faculty of Medicine, Lecturer, 医学部附属病院, 講師 (50251286)
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| Co-Investigator(Kenkyū-buntansha) |
IWASAKI Shinichi The University of Tokyo, Faculty of Medicine, Assistant, 医学部附属病院, 助手 (10359606)
MATSUI Minoru The University of Tokyo, The Institute of Medical Science, Assistant, 医科学研究所, 助手 (50282611)
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2005: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2004: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2003: ¥2,200,000 (Direct Cost: ¥2,200,000)
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| Keywords | muscarinic receptor / subtype / knock-out mice / patch clamp / spiral ganglion / vestibular ganglion / dissociated cells / 聴性脳幹反応(ABR) / 内耳単離細胞 |
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| Research Abstract |
This year, we continued our research on the basis of what we have established during the past two years. However, we encountered two troubles at the beginning of the year. First, because of epidemic problems, supply of the knock-out animals was disconnected for about half a year. The stable supply was re-established in November and we resumed the experiments. Secondly, in the meantime, a competing laboratory in the States reported that their mice lacking muscarinic receptors (product independent of our knock-outs) had almost normal hearing and similar susceptibility to ototoxic agents (Maison SF, et al. 2005).
However, we made progress in two points. First, we revised the computer software to record OAEs, which was a pending problem from the last year, and enabled recording DPOAEs in animals as well as in humans. Secondly, considering the situation described above, we tried to shift the axis of our research in the inner ear from the auditory system to the vestibular system and finally w
… More
ere able to record action potentials of vestibular ganglion cells in rodents on the whole-cell patch clamp mode. We also revealed the expression of mRNAs for muscarinic receptors in vestibular ganglion cells by means of DNA arrays.
Planned studies in the near future :
1) We still continue the experiments on comparative studies on susceptibility to extraordinary noise and to ototoxic drugs using knock-out and wild-type mice. This is because the results may differ from those from the USA group, since the knock-out mice were independently produced.
2) Since the existence of muscarinic receptors on the vestibular ganglion cells in rodents was indicated, we plan first to investigate modulation of excitability of neurons by muscarinic receptors and then to reveal the difference of neuronal firing patterns between knock-out and wild-type mice. Moreover, by investigating the difference in contribution of ionic channels on action potential formation, the contribution of muscarinic receptors to developmental processes of vestibular ganglion cells will be deduced. Less
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Report
(4 results)
Research Products
(8 results)
