首页> 外文期刊>Microscopy and microanalysis: The official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada >Three-Dimensional Microvasculature in Rat and Human Hearts Using a Non-injection Ca~(2+) -ATPase Method on Thick and Ultra-Thick Sections
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Three-Dimensional Microvasculature in Rat and Human Hearts Using a Non-injection Ca~(2+) -ATPase Method on Thick and Ultra-Thick Sections

机译:使用非注射Ca〜(2 +)-ATPase方法在大鼠和人心脏上的三维微脉管系统的厚和超厚切片

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摘要

Currently there are no methods available for staining rat and human myocardial microvasculature on thick sections that would allow for specific staining and differentiation of arterioles, venules, and capillaries. A non-injection technique is described that allows for labeling of the microvascular bed (MVB) in formalin-fixed pieces of the myocardium from humans and the white rat Rattus norvegicus, as well as human full-mount pericardium. Vessel staining is based on the activity of phosphatases (ATPases) and the precipitation of the released phosphate with calcium ions at high pH (pH 10.5–11.5). The resulting precipitate subsequently is converted to black or brown lead sulfide. The specificity of this reaction to vessels of the MVB allows arterioles, venules, capillaries, and pre- and postcapillaries to be clearly visualized in thick (60–100 μm) and ultra-thick (300–500 μm) sections against an unstained background of muscle and connective tissue. In addition, smooth muscle cells of arterioles are also stained allowing for differentiation between arteriolar and venular beds. These observations have not been reported in rat or human myocardium using other methods. This procedure should benefit studies of coronary microcirculation in experimental and pathological conditions, as well as in pharmacological investigations.
机译:当前,尚无可用于在厚切片上对大鼠和人的心肌微血管进行染色的方法,这些方法无法对小动脉,小静脉和毛细血管进行特定的染色和分化。描述了一种非注射技术,该技术可以标记人和白鼠褐家鼠以及人类全心包的心包福尔马林固定的心肌中微血管床(MVB)。血管染色是基于磷酸酶(ATPases)的活性以及在高pH(pH 10.5-11.5)下钙离子释放的磷酸盐的沉淀。随后将所得沉淀物转化为黑色或棕色硫化铅。该反应对MVB血管的特异性使小动脉,小静脉,毛细血管以及毛细血管前和毛细血管形成清晰可见,厚膜片(60–100μm)和超厚膜片(300–500μm),未染色的背景肌肉和结缔组织。另外,小动脉的平滑肌细胞也被染色,以允许区分小动脉和静脉床。使用其他方法尚未在大鼠或人类心肌中报告这些观察结果。该程序应有益于在实验和病理条件下进行冠状动脉微循环的研究以及药理研究。

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