2010 Fiscal Year Final Research Report
Can we prevent overactive bladder?
Project/Area Number |
20591880
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Urology
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Research Institution | Tottori University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
KINOSHITA Yukako 鳥取大学, 医学部, 助教 (50032214)
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Project Period (FY) |
2008 – 2010
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Keywords | 過活動膀胱 |
Research Abstract |
Bladder dysfunction in a rat model caused by acute urinary retention(AUR) needs more than two weeks of recovery period, and within two weeks of induction of AUR these rats may be used as a rat overactive bladder(OAB) model. A radical scavenger, edaravone reduces the oxidative stress and prevents the bladder dysfunction caused by AUR and subsequent catheterization. K_<ATP> channel openers, nicorandil and cromakalim prevent AUR-induced bladder dysfunction via activation of K_<ATP> channels with subsequent decrease in oxidative stress and decreased induction of apoptosis. Chronic administration of a K_<ATP> channel opener, nicorandil, anα_<1A>-blocker, silodosin, and a Rho kinase inhibitor, fasdil ameliorate hypertension-related bladder dysfunction in the SHR via improvement of bladder blood flow.
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