Direct in vivo visualization of human renal microcirculation using less-invasive intravital videomicroscopy. -vascular structure and renal blood flow-
Direct in vivo visualization of human renal microcirculation using less-invasive intravital videomicroscopy. -vascular structure and renal blood flow-
批准号:
12671569
负责人:
TANAKA Hiroyoshi
金额:
$2.5万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2001
中文摘要
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英文摘要
Several technical approaches for the evaluation of renal microcirculation have been developed Although each methodology possesses unique advantages, their common disadvantage is in the need for substantial manipulation on the kidney that might alter the renal microvascular responsiveness.To circumvent this drawback of previous approaches to renal microcirculation, we have developed a pencil-lens probe ($ 1mm, length : 25cm, weight 160g) with the charge-coupled divice (CCD) intravital videomicroscopic system (spatial resolution : 0.86um, time resolution : 30 frame/sec), which combines the characteristics ofmicroscopy and endoscopy. This system allowed us to perform less- invasive evaluation of both the renal structure and microcirculation approach to laparoscopic hole and open operation. Furthermore, real-time imaging of afferent and efferent arterioles, as well as glomeruli can be continuously assessed, thus permitting the functional characterization of microcirculation. A line segment was set along the glomerular capillaries and then a spatiotemporal image was constructed along the segment. The angle of stripped pattern in the spatiotempolar image, which is related to the erythrocyte velocity, was applied to compute erythrocyte velocity vectors as previously reported from Ogasawara et al group. Motion analysis of sequential images yields data on velocity of erythrocytes and leukocytes in glomeruli. In conclusion, this less-invasive technique will reveal as yet unknown field of renal microcirculation.
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Yamamoto T: "Direct In Vivo Visualization of Renal Microcirculation by Intravital CCD Videomicroscopy."Experimental Nephrology.. 9・2. 150-155 (2001)
Yamamoto T:“通过活体 CCD 视频显微镜直接体内观察肾脏微循环。”实验肾病学.. 9・2。
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Yamamoto, T.: "In vivo visualization of characteristics of renal microcirculation in hypertensive and diabetic rats"Am J Physiol Renal Physiol. 281. F571-F577 (2001)
Yamamoto, T.:“高血压和糖尿病大鼠肾脏微循环特征的体内可视化”Am J Physiol Renal Physiol。
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Yamamoto, T.: "In vivo visualization of angiotensin II-and tubuloglomerular feedback-mediated renal vasoconstriction"Kidney Int. 60・1. 364-369 (2001)
Yamamoto, T.:“血管紧张素 II 和肾小球反馈介导的肾血管收缩的体内可视化”Kidney Int. 60・1 (2001)。
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Yamamoto, T.: "Direct in vivo visualization of glomerular microcirculation by intravital pencil lens-probe CCD videomicroscopy"Clin Hemorheol Microcirc. 23・2-4. 103-108 (2000)
Yamamoto, T.:“通过活体铅笔透镜探针 CCD 视频显微镜直接体内观察肾小球微循环”Clin Hemorheol Microcirc。
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山本徳則: "糸球体微小循環の薬理的評価-新規in vivoバイオイメージング法を用いて-"日本薬理学会誌. 82・Suppl.I. 25 (2000)
Norinori Yamamoto:“肾小球微循环的药理学评价 - 使用新的体内生物成像方法 -”日本药理学会杂志 82・增刊 25(2000)。
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共 24 条
Frictional performance of mixed metal soap greases
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批准号:18560136
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.3万
-
财政年份:2006
-
负责人:TANAKA Hiroyoshi
-
依托单位:
In vivo vizualization of glomerular microcirculation microcirculation in AT1 a knock-out mice. -Role of anigiotensinII-
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批准号:10671506
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.66万
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财政年份:1998
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负责人:TANAKA Hiroyoshi
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依托单位:
In vivo observation of intrarenal microvessels and evaluation of the effect of exgenous high dose Angiotensin II forrenal microcirculation by a needle probe video microscope with a CCD camera.
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批准号:08671850
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.47万
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财政年份:1996
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负责人:TANAKA Hiroyoshi
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依托单位:
Newly development of CCD videomicroscope with a fine needle probe of side and straight angle mirror
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批准号:07557255
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$0.51万
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财政年份:1995
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负责人:TANAKA Hiroyoshi
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依托单位:
海外基金