The investigation into the molecular and electrophysiological properties of overactive bladder and the research for the novel consequent treatment
| Project/Area Number |
20599012
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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 |
Urology
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| Research Institution | Kyushu University |
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Principal Investigator |
KAJIOKA Shunichi Kyushu University, 医学研究院・泌尿器科学 (90274472)
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| Co-Investigator(Kenkyū-buntansha) |
SEKI Narihito 九州大学, 大学院・医学研究院, 准教授 (90294941)
NAKAYAMA Shinsuke 名古屋大学, 大学院・医学研究科, 准教授 (30192230)
ITO Shinichi 九州大学, 大学院・歯学研究院, 助教 (00315095)
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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 |
¥3,940,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥540,000)
Fiscal Year 2010: ¥520,000 (Direct Cost: ¥400,000、Indirect Cost: ¥120,000)
Fiscal Year 2009: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2008: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | 膀胱排尿筋 / 過活動膀胱 / イオンチャネル / 特殊間質性細胞 / カルシウムオシレーション / 特殊間質性細 |
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| Research Abstract |
The molecular and electrophysiological properties of ATP-sensitive K+ channel were clarified in pig detrusor smooth muscle (Kajioka et al. J Pharmacol Exp Ther 2008). Also in human detrusor smooth muscle, the single channel current of ATP-sensitive K+channel were successfully recorded and this channel was activated by β-nicotinamide adenine dinucleotide (βNAD) (Kajioka et al. J Urol 2011 in press).
Western Blotting and immunohistochemical staining failed to reveal the significant predominant increase of ckit-positive interstitial cell or gap junction in the outlet obstruction bladder of guinea pig. However, immunohistochemical staining demonstrated that the expression of both M2 and M3 muscarinic receptor subtypes were increased by the obstruction. As for Ca2+ sensitization in human detrusor, we concluded that M3 receptor had a predominant role and comparable contribution to ROK and PKC pathways while it M2 receptor mediated ROK pathway via the down regulation of cAMP.
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Report
(4 results)
Research Products
(37 results)
