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In-vivo Visualisation of glomerular filtration by two-photon microscopy in a rat

机译:在大鼠中通过双光子显微镜对肾小球滤过的体内可视化

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The purpose of this study was to visualise and evaluate glomerular filtration quantitatively under physiological conditions in a rat.We used normal Wistar rats. Various sizes of dextran (3k, 10k, 40k and 70kDa) conjugated with Texas Red in 0.5 ml were administered intravenously by bolus shot and for the next 80 seconds glomerular filtration was observed by two-photon microscopy (Leica TCS SP2). In this way, glomerular filtration was visualised. FITC conjugated 500kDa dextran was administered to dye intravascular area prior to experiment. The time course of Texas Red intensity in Bowman's space was measured off-line later. Intensity peak values were normalised for comparison by the peak value of 3 k Da as sieving coefficients.Filtration of the smaller dextrans (MW 3k and l0kDa) was clearly visualized by two-photon microscopy in rats. Filtration of the larger dextrans (MW 40k and 70kDa) was also found indicating leakage of the size of albumin molecule even in a normal rat.Glomerular filtration in a rat was clearly visualised by two-photon microscopy and leakage of larger particles of 70kDa dextran was found even in a normal rat. Two-photon laser microscopy is a powerful tool to investigate renal glomerular functions quantitatively.
机译:这项研究的目的是可视化和评估大鼠在生理条件下的肾小球滤过。 我们使用了普通的Wistar大鼠。通过推注静脉内注射0.5 ml与德克萨斯红共轭的各种大小的右旋糖酐(3k,10k,40k和70kDa),并在接下来的80秒内通过双光子显微镜(Leica TCS SP2)观察肾小球滤过。这样,肾小球滤过被可视化。在实验之前,将FITC缀合的500kDa葡聚糖施用至染色血管内区域。后来离线测量了鲍曼空间中德克萨斯红强度的时程。通过3 k Da的峰值作为筛分系数对强度峰值进行标准化以进行比较。 通过双光子显微镜在大鼠中清楚地观察到较小的葡聚糖(MW 3k和10kDa)的过滤。还发现较大的葡聚糖(分子量为40k和70kDa)的过滤表明即使在正常大鼠中白蛋白分子的大小也会泄漏。 通过双光子显微镜清楚地观察了大鼠的肾小球滤过,甚至在正常大鼠中也发现了较大的70kDa葡聚糖颗粒泄漏。双光子激光显微镜是定量研究肾小球功能的有力工具。

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