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MULTIMODAL ASSESSMENT OF HEPATOCYTE GROWTH FACTOR ANGIOGENIC GENE THERAPY IN RAT MYOCARDIAL INFARCT MODEL. 

https://repo.qst.go.jp/records/70238
https://repo.qst.go.jp/records/70238
7afe14e4-a975-4141-9959-87aea4202156
Item type 会議発表用資料 / Presentation(1)
公開日 2010-09-14
タイトル
タイトル MULTIMODAL ASSESSMENT OF HEPATOCYTE GROWTH FACTOR ANGIOGENIC GENE THERAPY IN RAT MYOCARDIAL INFARCT MODEL. 
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 Nan, Jin Yong

× Nan, Jin Yong

WEKO 689691

Nan, Jin Yong

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Inubushi, Masayuki

× Inubushi, Masayuki

WEKO 689692

Inubushi, Masayuki

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Masamoto, Kazuto

× Masamoto, Kazuto

WEKO 689693

Masamoto, Kazuto

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Odaka, Kenichi

× Odaka, Kenichi

WEKO 689694

Odaka, Kenichi

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Aoki, Ichio

× Aoki, Ichio

WEKO 689695

Aoki, Ichio

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Tsuji, Atsushi

× Tsuji, Atsushi

WEKO 689696

Tsuji, Atsushi

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Sagara, Masashi

× Sagara, Masashi

WEKO 689697

Sagara, Masashi

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Koizumi, Mitsuru

× Koizumi, Mitsuru

WEKO 689698

Koizumi, Mitsuru

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 689699

Saga, Tsuneo

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金 永男

× 金 永男

WEKO 689700

en 金 永男

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犬伏 正幸

× 犬伏 正幸

WEKO 689701

en 犬伏 正幸

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正本 和人

× 正本 和人

WEKO 689702

en 正本 和人

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小高 謙一

× 小高 謙一

WEKO 689703

en 小高 謙一

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青木 伊知男

× 青木 伊知男

WEKO 689704

en 青木 伊知男

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辻 厚至

× 辻 厚至

WEKO 689705

en 辻 厚至

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相良 雅史

× 相良 雅史

WEKO 689706

en 相良 雅史

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小泉 満

× 小泉 満

WEKO 689707

en 小泉 満

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佐賀 恒夫

× 佐賀 恒夫

WEKO 689708

en 佐賀 恒夫

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抄録
内容記述タイプ Abstract
内容記述 Hepatocyte growth factor (HGF) has been shown to have a potent angiogenic activity in vitro, however, the in vivo therapeutic effects of angiogenic gene therapy using HGF gene in ischemic heart disease remains controversial. The aim of this study was to investigate the effects of HGF gene therapy in rat myocardial infarct model precisely with multimodal imaging including cine MRI, SPECT/CT, and two-photon excitation fluorescent microscopy (TPEFM).
Human sodium-iodide symporter (hNIS) gene was used as a radionuclide reporter gene. Recombinant adenoviruses expressing both HGF and hNIS genes comparably driven by dual constitutive cytomegalovirus promoters (Ad-CMV-HGF-CMV-hNIS; Treatment) and hNIS gene only (Ad-CMV-hNIS; Control) were constructed. Wister rats (10 week-old male) received permanent ligation of the left anterior descending artery, followed by injection of Treatment or Control vector into peri-infarct regions of the left ventricular myocardium. On Day 1, cine MRI was performed using a 7.0T MRI (Bruker Biospin BGA-1) to measure end-diastolic volume (EDV) and ejection fraction (EF). On Days 2 and 4, SPECT/CT images of therapeutic gene expression and myocardial perfusion were obtained with 99mTcO4- and 99mTc-tetrofosmin using a small animal SPECT/CT (Gamma Medica-Ideas FX). Nine (5 Treatment and 4 Control) rats showing similar infarct size and similar gene expression levels were followed for 10 weeks to repeat cine MRI and SPECT/CT. Afterwards, excised hearts were processed for immunohistochemistry with alpha-SMA and CD31 to measure small blood vessels and capillary density, and TPEFM to visualize the three-dimensional microvasculature.
The repeated cine MRI demonstrated significantly increased EDV in both Treatment and Control rats without significant difference between the groups. The infarct size was similar after follow-up. Capillary density defined by immunohistochemistry was significantly higher in Treatment rats, while small blood vessels were comparable between the groups. TPEFM revealed very thin (≈2µm) irregular vessels increased at peri-infarct regions of Treated hearts.
TPEFM provided direct evidence that sole HGF gene therapy could induce exclusively immature dysfunctional vessels, which explains other results that increased capillary density didn't lead to cardiac functional recovery. This may contribute to solve the gap between promising results from basic researches and lack in decisive therapeutic effects in clinical researches.
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 World Molecular Imaging Congress 2010
発表年月日
日付 2010-09-11
日付タイプ Issued
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