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Dynamical O-17 imaging in tumor bearing mice at 7T

https://repo.qst.go.jp/records/62126
https://repo.qst.go.jp/records/62126
7b4441e2-47e7-4a9f-8f93-53d9c7d21892
Item type 会議発表用資料 / Presentation(1)
公開日 2007-06-20
タイトル
タイトル Dynamical O-17 imaging in tumor bearing mice at 7T
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Narazaki, Michiko

× Narazaki, Michiko

WEKO 614442

Narazaki, Michiko

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Kanazawa, Yoko

× Kanazawa, Yoko

WEKO 614443

Kanazawa, Yoko

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Koike, Sachiko

× Koike, Sachiko

WEKO 614444

Koike, Sachiko

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Ando, Koichi

× Ando, Koichi

WEKO 614445

Ando, Koichi

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Ikehira, Hiroo

× Ikehira, Hiroo

WEKO 614446

Ikehira, Hiroo

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楢崎 美智子

× 楢崎 美智子

WEKO 614447

en 楢崎 美智子

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金沢 洋子

× 金沢 洋子

WEKO 614448

en 金沢 洋子

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小池 幸子

× 小池 幸子

WEKO 614449

en 小池 幸子

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安藤 興一

× 安藤 興一

WEKO 614450

en 安藤 興一

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池平 博夫

× 池平 博夫

WEKO 614451

en 池平 博夫

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抄録
内容記述タイプ Abstract
内容記述 Introduction: Oxygen consumption rate and blood flow are important parameters for the physiological and pathological evaluation of brain,
myocardium and tumors1,2, where 15O PET has been utilized.
17O MRI will be another tool for the direct observation of tumor oxygenation.
Measurements of the blood flow and oxygen consumption rate by in vivo
17O NMR has been reported recently3,4. We have developed 17O
imaging by FISP and succeeded in the visualization of natural abundance H217O distribution in the mouse with 10 min data acquisition5. In this
study, we will report the dynamical study of 17O imaging using 17O enriched saline in the tumor bearing mice. Phantom experiments
demonstrated the feature of 17O in vivo NMR signals.
Methods: MRS/MRI was performed on 7T/400mm/SS system (NIRS/KOBELCO/Bruker) with 40 mm 1H/17O Litz coil (Doty Scientific Inc.).
Water, ethanol or 25-100 % ethyleneglycol -water was used in phantom experiments.
17O images of healthy and tumor bearing C3H/He mice
(20 . 25 g) were obtained under Ketamine:Xylazine anesthesia by true FISP with a TR/TE = 4.3/2.15 ms.
A saline (0.5ml) containing 5% 17O
prepared from 10% 17O water (Cambridge Isotope Laboratories, Inc) was i.v. injected to tumor bearing mice.
After imaging experiment, organs
were excised for 17O spectral measurements.
Results: Phantom studies: The 17O signal of ethyleneglycol or water in 25% ethyleneglycol-water phantom was detected by fid acquisition
mode but not by echo mode within our experimental condition.
Animal studies: The S/N in the 17O images of a mouse obtained by FISP with
10 min data acquisition was dramatically improved from 3.8 to 13.4 after the injection of a saline containing 5% 17O. The result of 10 sec
dynamical imaging of H217O with under the spatial resolution of 2.5 mm without slicing was shown in Fig.1. The process of initial
accumulation of the injected H217O in the heart and re-distribution to whole body was demonstrated.
Spatial resolution of 1.25 mm was attained
with the 10 min data acquisition.
Discussion: The dynamical study of H217O was achieved in the tumor bearing mice with a temporal resolution of 10 sec.
The temporal and
spatial resolutions attained in this study will lead this imaging method to the evaluation of blood flow or oxygen consumption rate using 17O gas
and water. FISP is shown to be an effective method for imaging in vivo
17O signals from free water. The phantom experiments with
ethyleneglycol-water strongly suggest that the in vivo 17O images obtained here is from the mobile H217O and not from other molecular species or
immobilized water. The echo image of 17O detecting solely the signal from free water, not from the body constituents contributing as
background should have an advantage over the other NMR method with FID detection in the 17O2 gas study.
Reference:
(1) Secomb TW. et al, 34 :313 (1995), (2) Ando K, et al, Int J Radiat Biol 75 :505 (1999), (3) Zhu XH. et al, MRM 45:543 (2001), (4) Fiat D. et al,
Neurol Res 26:803 (2004), (5) Narazaki M. et al, 14th ISMRM 3113 (2006)
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 Joint Annual Meeting ISMRM-ESMRMB 2007
発表年月日
日付 2007-05-25
日付タイプ Issued
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