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Hemodynamic changes in crossed cerebellar diaschisis measured by Laser-Doppler flowmetry in awake mice

https://repo.qst.go.jp/records/65019
https://repo.qst.go.jp/records/65019
5e1e5ded-70e1-4d29-afcf-e72009e3d19f
Item type 会議発表用資料 / Presentation(1)
公開日 2013-05-29
タイトル
タイトル Hemodynamic changes in crossed cerebellar diaschisis measured by Laser-Doppler flowmetry in awake mice
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 Takuwa, Hiroyuki

× Takuwa, Hiroyuki

WEKO 640683

Takuwa, Hiroyuki

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Tajima, Yousuke

× Tajima, Yousuke

WEKO 640684

Tajima, Yousuke

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Kawaguchi, Hiroshi

× Kawaguchi, Hiroshi

WEKO 640685

Kawaguchi, Hiroshi

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Taniguchi, Jyunko

× Taniguchi, Jyunko

WEKO 640686

Taniguchi, Jyunko

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Ikoma, Youko

× Ikoma, Youko

WEKO 640687

Ikoma, Youko

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Masamoto, Kazuto

× Masamoto, Kazuto

WEKO 640688

Masamoto, Kazuto

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Seki, Chie

× Seki, Chie

WEKO 640689

Seki, Chie

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Kanno, Iwao

× Kanno, Iwao

WEKO 640690

Kanno, Iwao

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Ito, Hiroshi

× Ito, Hiroshi

WEKO 640691

Ito, Hiroshi

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田桑 弘之

× 田桑 弘之

WEKO 640692

en 田桑 弘之

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田島 洋佑

× 田島 洋佑

WEKO 640693

en 田島 洋佑

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川口 拓之

× 川口 拓之

WEKO 640694

en 川口 拓之

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谷口 順子

× 谷口 順子

WEKO 640695

en 谷口 順子

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生駒 洋子

× 生駒 洋子

WEKO 640696

en 生駒 洋子

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正本 和人

× 正本 和人

WEKO 640697

en 正本 和人

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関 千江

× 関 千江

WEKO 640698

en 関 千江

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菅野 巖

× 菅野 巖

WEKO 640699

en 菅野 巖

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伊藤 浩

× 伊藤 浩

WEKO 640700

en 伊藤 浩

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抄録
内容記述タイプ Abstract
内容記述 Objectives: Neural activation has been reported to cause larger increase in cerebral blood flow (CBF) than cerebral blood volume (CBV) in humans using PET [1] and has been reported to cause larger increases in red blood cell RBC velocity than RBC concentration in mice using Laser-Doppler flowmetry (LDF) [2]. Crossed cerebellar diaschisis (CCD) caused by contralateral supratentorial lesions can be considered as a condition of neural deactivation, and hemodynamic changes in CCD measured with positron emission tomography (PET) in humans have been reported to show almost the same degree of decrease in CBF and CBV [3]. In the present study, we developed a new mouse model of CCD and measured the change in RBC velocity and concentration due to CCD using LDF.
Methods: RBC velocity and concentration were measured with LDF through a chronic cranial window at the cerebellum in awake mice (C57BL/6J mice, 27-30g, N=6) riding our custom-made apparatus [4]. This apparatus consisted of a head holder and styrofoam ball float on a jet of air under the mice. This allows the mice to walk freely on the ball during LDF measurement. RBC velocity and concentration in bilateral cerebellum were measured at baseline and one day after permanent occlusion of contralateral middle cerebral artery (MCAO) which can cause CCD. The ratio of CCD side to unaffected side in cerebellum for measures by LDF was calculated.
Results: The ratio of CCD side to unaffected side in cerebellum for CBF corresponding to RBC velocity multiplied by RBC concentration after MCAO was decreased by -18% as compared to that of baseline. The ratio of CCD side to unaffected side in cerebellum for RBC concentration after MCAO was decreased by -23% as compared to that of baseline. However, no significant changes in the ratio of CCD side to unaffected side in cerebellum were observed for RBC velocity.
Discussion: The present results indicate that reduction of CBF induced by neural deactivation was mainly caused by the decrease in RBC concentration. The relationship between changes in RBC velocity and concentration due to a neural deactivation is opposite to those due to a neural activation [3]. If RBC concentration can be used as an indicator of CBV, hemodynamic changes due to neural activation and deactivation measured by LDF might be in good agreement with PET measurement in humans previously reported [1,3]. It is likely that our newly established mouse model of CCD will be useful for investigation of the effects of neural deactivation on cerebral microcirculation using two-photon laser microscope and animal PET.
References:
[1] Ito H, et al. J Cereb Blood Flow Metab 2005; 25: 371-377.
[2] Takuwa H, et al. Brain Res. 2012; 1472; 107-112
[3] Ito H, et al. Ann Nucl Med 2002; 16: 249-254.
[4] Takuwa H, et al. Brain Res. 2011; 1369; 103-111
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 Brain & Brain PET 2013
発表年月日
日付 2013-05-23
日付タイプ Issued
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