Relationship between cerebral perfusion/neuronal activity and amyloid deposition
Project/Area Number |
23591809
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Radiation science
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Research Institution | National Institute of Radiological Sciences |
Principal Investigator |
SEKI Chie 独立行政法人放射線医学総合研究所, 分子イメージング研究センター, 研究員 (40443080)
|
Co-Investigator(Renkei-kenkyūsha) |
HIGUCHI Makoto 独立行政法人放射線医学総合研究所, 分子イメージング研究センター, チームリーダー (10373359)
|
Project Period (FY) |
2011 – 2013
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
|
Keywords | 放射線 / 脳神経疾患 / 痴呆 / 老化 |
Research Abstract |
It has been considered that decreased cerebral blood flow may accelerate Alzheimer's disease (AD) related pathologies. To investigate the impact of lowered regional cerebral blood flow (rCBF) on the formation of amyloid beta (Abeta) deposition, unilateral cerebral hypoperfusion model was made on amyloid precursor protein transgenic (APP Tg) mice by the ligation of the left common carotid artery. The progression of Abeta depositions and rCBF were quantitatively monitored with [11C]PIB-PET and MRI over months. The rCBF of ipsilaterel neocortex sustained up to 84% of that of contralateral neocortex. The Abeta deposition increased and expanded over time without laterality related to hypoperfusion. The current results indicate that chronic cerebral hypoperfusion is not considered to accelerate deposition of Abeta plaques. In vivo imaging technologies such as PET and MRI have advantageous to visualize alterations of Abeta depositions and rCBF in living model mouse brains longitudinally.
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Report
(4 results)
Research Products
(11 results)
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[Presentation] Chronic cerebral hypoperfusion did not accelerate [11C]PIB-reactive Abeta deposition in amyloid precursor protein transgenic mice2013
Author(s)
Seki C, Higuchi M, Tokunaga M, Maruyama M, Ono M, Jin B, Maeda J, Nitta N, Aoki I, Suhara T, Ito H
Organizer
XXVIth International Symposium on Cerebral Blood Flow, Metabolism and Function
Place of Presentation
Shanghai, China
Related Report
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[Presentation] Chronic cerebral hypoperfusion did not accelerate [11C]PIB-reactive Abeta deposition in amyloid precursor protein transgenic mice.2013
Author(s)
Seki C, Higuchi M, Tokunaga M, Maruyama M, Ono M, Jin B, Maeda J, Nitta N, Aoki I, Suhara T, Ito H
Organizer
XXVIth International Symposium on Cerebral Blood Flow, Metabolism and Function.
Place of Presentation
Shanghai International Convention Center, Shanghai, China
Related Report
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[Presentation] Relationship between kinetic parameters of [11C]PIB and amyloidβdeposition studied in amyloid precursor protein transgenic mouse brains2012
Author(s)
Seki C, Tokunaga M, Hattori S, Murayama M, Ono M, Ji B, Maeda J, Suhara T, Higuchi M, Ito H
Organizer
Neuroreceptor Mapping Congress
Place of Presentation
Johns Hopkins University, Baltimore, Maryland, U.S.A
Related Report
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[Presentation] Evaluation of regional cerebral blood flow using [^<11>C]PIB in unilateral cerebral hypoperfusion model mice2011
Author(s)
Seki C, Higuchi M, Saito S, Tokunaga M, Maruyama M, Okauchi T, Aoki I, Ito H, and Suhara T
Organizer
Annual Meeting of Society for Neuroscience 2011
Place of Presentation
Washington Covention Center, Washington, D.C., USA
Related Report
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[Presentation] Evaluation of regional cerebral blood flow using [11C]PIB in unilateral cerebral hypoperfusion model mice.2011
Author(s)
Seki C, Higuchi M, Saito S, Tokunaga M, Maruyama M, Okauchi T, Aoki I, Ito H, and Suhara T
Organizer
Annual Meeting of Society for Neuroscience 2011
Place of Presentation
Washington Covention Center, Washington, D.C., USA.
Related Report
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