The elucidation of the intracerebral transporter control to lead the new cerebroprotection method
Project/Area Number |
20591818
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Anesthesiology/Resuscitation studies
|
Research Institution | Tokyo Medical University |
Principal Investigator |
MUROZONO Michihiro Tokyo Medical University, 医学部, 講師 (70276947)
|
Co-Investigator(Kenkyū-buntansha) |
岡田 真也 東京医科大学, 医学部, 講師 (20297279)
|
Project Period (FY) |
2008 – 2010
|
Project Status |
Completed (Fiscal Year 2010)
|
Budget Amount *help |
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2010: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2009: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2008: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
|
Keywords | 脳虚血 / mdr1a / 血液脳関門 / P-glycoprotein / サイトカイン / P-glucoprotein / ノックアウトマウス |
Research Abstract |
There is mdr1a intracranially, which blocks invasion of multi drug to brain. Mdr1 also influences displacement of endogenous substance. We made a focal cerebral ischemia model using mdr1a knockout mouse and measured blood cytokine and apoptosis-related substances such as Bcl-2 in brain. From the results, we suggest that mdr1a influences IL-6, Bcl-2 and Bax after cerebral ischemia and promotes the damage to brain.
|
Report
(4 results)
Research Products
(13 results)