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Persistent failure of neurovascular coupling induced by prolonged moderate hypoxia in the somatosensory cortex in mice

https://repo.qst.go.jp/records/70625
https://repo.qst.go.jp/records/70625
784e1b4d-c344-4ff5-ad15-1f596e4c6992
Item type 会議発表用資料 / Presentation(1)
公開日 2011-11-21
タイトル
タイトル Persistent failure of neurovascular coupling induced by prolonged moderate hypoxia in the somatosensory cortex in 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 Kanno, Iwao

× Kanno, Iwao

WEKO 693705

Kanno, Iwao

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Masamoto, Kazuto

× Masamoto, Kazuto

WEKO 693706

Masamoto, Kazuto

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Takuwa, Hiroyuki

× Takuwa, Hiroyuki

WEKO 693707

Takuwa, Hiroyuki

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Kawaguchi, Hiroshi

× Kawaguchi, Hiroshi

WEKO 693708

Kawaguchi, Hiroshi

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Taniguchi, Jyunko

× Taniguchi, Jyunko

WEKO 693709

Taniguchi, Jyunko

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Tomita, Yutaka

× Tomita, Yutaka

WEKO 693710

Tomita, Yutaka

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Suzuki, Norihiro

× Suzuki, Norihiro

WEKO 693711

Suzuki, Norihiro

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Ito, Hiroshi

× Ito, Hiroshi

WEKO 693712

Ito, Hiroshi

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菅野 巖

× 菅野 巖

WEKO 693713

en 菅野 巖

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正本 和人

× 正本 和人

WEKO 693714

en 正本 和人

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田桑 弘之

× 田桑 弘之

WEKO 693715

en 田桑 弘之

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川口 拓之

× 川口 拓之

WEKO 693716

en 川口 拓之

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谷口 順子

× 谷口 順子

WEKO 693717

en 谷口 順子

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冨田 裕

× 冨田 裕

WEKO 693718

en 冨田 裕

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伊藤 浩

× 伊藤 浩

WEKO 693719

en 伊藤 浩

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抄録
内容記述タイプ Abstract
内容記述 The effects of prolonged moderate hypoxia on the neurovascular coupling were examined in mice. One week before the experiments a cranial window was opened above the somatosensory cortex of C57BL/6J mice. The mice were slowly adapted (in 1.5 hours at first) into a hypoxia chamber (2.4 L) with two hypoxia levels (8% oxygen (n=6) and 10% oxygen (n=5)) for one month. Two of the 8% oxygen mice were further kept alive for another two months in room air. Cortical CBF responses to air puffs (10Hz for 20 sec) were weekly measured using LDF. All measurements were done in awake and the mice kept free motion on a floating ball. The cranial window was fixed to the stage of a two-photon microscope and 3D images with 0.5 micrometer x-y resolution were acquired individually at the same parenchymal location after intraperitoneal injection of sulforhodamine 101 as fluorescent dye. Hematocrit at week 1, 2 and one month was measured using separate mice of 8% oxygen. The 8% oxygen mice revealed a declined CBF responses week-by-week from 25% to < 5% in one month, though the 10% oxygen mice showed almost consistent CBF responses around 25% over one month. The two 8% oxygen mice kept alive for another two months in room air demonstrated sustained failure of CBF response. In 8% oxygen mice, the hematocrit was increased from 35 to 68 in one month. Since locomotion levels evoked by air-puffs were unchanged during the experiment period for both the 8% and 10% oxygen groups, it is plausible that the cortical neuronal function was intact during course of the experiment. Morphological change to the microvessels may not be a possible explanation for the decreased CBF response because the failure was sustained even when the microvessel diameter returned to the baseline level after the mice to room air for more than two months. However, the 8% oxygen mice demonstrated gradual increase in astroglia cell areas by 50%. Therefore, the failure of the neurovascular coupling might be caused by disruption of signal transmission between the neuron and the microvessel, e.g. malfunction in the pathways either from neuron to astroglia, from astroglia to the endothelium, or from endothelium to smooth muscle. Further experiments are necessary to confirm and clarify these questions, that is, measurements of cortical neuronal activity, and vascular responses to carbon dioxide (CO2) and/or to sodium nitroprusside (SNP; NO donor). In conclusion, circumstance to 8% oxygen for one month induced to fail the CBF response to somatosensory stimulation in mice. This could be used as a new model to study inhibition of the neurovascular coupling.
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 Neuroscience 2011
発表年月日
日付 2011-11-16
日付タイプ Issued
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