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Changes in effective diffusivity for oxygen during neural activation and deactivation estimated from capillary diameter measured by two-photon laser microscope

https://repo.qst.go.jp/records/71123
https://repo.qst.go.jp/records/71123
e806f06a-f0e8-4fd4-93fc-a04b3fda06fc
Item type 会議発表用資料 / Presentation(1)
公開日 2013-05-31
タイトル
タイトル Changes in effective diffusivity for oxygen during neural activation and deactivation estimated from capillary diameter measured by two-photon laser microscope
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 Ito, Hiroshi

× Ito, Hiroshi

WEKO 699147

Ito, Hiroshi

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Takuwa, Hiroyuki

× Takuwa, Hiroyuki

WEKO 699148

Takuwa, Hiroyuki

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Tajima, Yousuke

× Tajima, Yousuke

WEKO 699149

Tajima, Yousuke

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Kawaguchi, Hiroshi

× Kawaguchi, Hiroshi

WEKO 699150

Kawaguchi, Hiroshi

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Masamoto, Kazuto

× Masamoto, Kazuto

WEKO 699151

Masamoto, Kazuto

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Taniguchi, Jyunko

× Taniguchi, Jyunko

WEKO 699152

Taniguchi, Jyunko

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Ikoma, Youko

× Ikoma, Youko

WEKO 699153

Ikoma, Youko

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Seki, Chie

× Seki, Chie

WEKO 699154

Seki, Chie

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Masanobu, Ibaraki

× Masanobu, Ibaraki

WEKO 699155

Masanobu, Ibaraki

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Kanno, Iwao

× Kanno, Iwao

WEKO 699156

Kanno, Iwao

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伊藤 浩

× 伊藤 浩

WEKO 699157

en 伊藤 浩

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田桑 弘之

× 田桑 弘之

WEKO 699158

en 田桑 弘之

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田島 洋佑

× 田島 洋佑

WEKO 699159

en 田島 洋佑

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川口 拓之

× 川口 拓之

WEKO 699160

en 川口 拓之

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正本 和人

× 正本 和人

WEKO 699161

en 正本 和人

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谷口 順子

× 谷口 順子

WEKO 699162

en 谷口 順子

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生駒 洋子

× 生駒 洋子

WEKO 699163

en 生駒 洋子

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関 千江

× 関 千江

WEKO 699164

en 関 千江

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茨木 正信

× 茨木 正信

WEKO 699165

en 茨木 正信

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菅野 巖

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WEKO 699166

en 菅野 巖

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抄録
内容記述タイプ Abstract
内容記述 Objectives: According to a model for the regulation of cerebral oxygen delivery proposed by Hyder et al. [1], the relation between cerebral blood flow (CBF) and cerebral oxygen extraction fraction (OEF) can be expressed using the effective diffusivity for oxygen in the capillary bed (D) as OEF=1-exp(-D/CBF). The D value is proportional to capillary blood volume, and therefore changes in D can be estimated from changes in capillary diameter. The discrepancy between the increases in CBF and cerebral metabolic rate of oxygen (CMRO2) during neural activation and deactivation observed in crossed cerebellar diaschisis (CCD) caused by contralateral supratentorial lesions has been reported to causes a significant decrease and increase in OEF using positron emission tomography (PET) in humans, respectively [2, 3]. In the present study, changes in D during neural activation and deactivation were estimated from changes in capillary diameter measured by in vivo two-photon laser microscopic imaging in mice, and compared with those calculated from measures by PET in humans reported previously.
Methods: The cortical vasculature was imaged with two-photon laser microscope through a chronic cranial window at the somatosensory cortex and cerebellum in awake mice (C57BL/6J mice, N=4) after intraperitoneal administration of sulforhodamine 101 (10 mM, 8 muL/g) for labelling blood plasma. First, capillary vessels diameter in the somatosensory cortex was measured at baseline and during sensory stimulation (Whisker stimulation: 10Hz). Second, capillary vessels diameter in the cerebellum was measured at baseline and one day after permanent occlusion of contralateral middle cerebral artery which could cause CCD. Changes in capillary diameter during neural activation and deactivation were calculated, and then changes in D were estimated. Changes in D during neural activation and deactivation caused by motor task and CCD, respectively, were also calculated as OEF=1-exp(-D/CBF) from measures by PET in humans previously reported [2, 3].
Results: Changes in capillary diameter were 6 +- 2% and -10 +- 3%, and changes in D were 13 +- 5% and -20 +- 6% during neural activation (somatosensory cortex) and deactivation (cerebellum) in mice, respectively. Changes in CBF, CMRO2, and OEF during neural activation by motor task reported in humans were 47%, 11%, and -24%, respectively, in the primary motor cortex, and therefore change in D calculated was 7% [2]. Changes in CBF, CMRO2, and OEF during neural deactivation by CCD reported in humans were -20%, -12%, and 8%, respectively, and therefore change in D calculated was -11% [3].
Conclusions: The degree of changes in D during both neural activation and deactivation were larger in mice than in humans, however the degree of changes in D during neural activation were smaller than during neural deactivation for both mice and humans. This might indicate the validity of a model for the regulation of cerebral oxygen delivery proposed by Hyder et al. [1].
References:
[1] Hyder F, et al. J Appl Physiol 1998; 85: 554-564.
[2] Ito H, et al. J Cereb Blood Flow Metab 2005; 25: 371-377.
[3] Ito H, et al. Ann Nucl Med 2002; 16: 249-254.
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 & BrainPET 2013
発表年月日
日付 2013-05-23
日付タイプ Issued
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