Dept. of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Am J Physiol Lung Cell Mol Physiol. 2013 Jan 15;304(2):L86-91. doi: 10.1152/ajplung.00178.2012. Epub 2012 Nov 16.
Intravital microscopy of the pulmonary microcirculation in research animals is of great scientific interest for its utility in identifying regional changes in pulmonary microcirculatory blood flow. Although feasibility studies have been reported, the pulmonary window can be further refined into a practical tool for pharmaceutical research and drug development. We have established a method to visualize and quantify dynamic changes in three key features of lung function: microvascular red blood cell velocity, flow direction, and hemoglobin saturation. These physiological parameters were measured in an acute closed-chest pulmonary window, which allows real-time images to be captured by fluorescence and multispectral absorption microscopy; images were subsequently quantified using computerized analysis. We validated the model by quantifying changes in microcirculatory blood flow and hemoglobin saturation in two ways: 1) after changes in inspired oxygen content and 2) after pharmacological reduction of pulmonary blood flow via treatment with the β1 adrenergic receptor blocker metoprolol. This robust and relatively simple system facilitates pulmonary intravital microscopy in laboratory rats for pharmacological and physiological research.
在研究动物的肺微循环的活体显微镜检查具有很大的科学意义,因为它可用于识别肺微循环血流的区域性变化。虽然已经有可行性研究的报道,但肺窗可以进一步细化为用于药物研究和药物开发的实用工具。我们已经建立了一种方法来可视化和量化肺功能的三个关键特征的动态变化:微血管红细胞速度、流动方向和血红蛋白饱和度。这些生理参数是在急性闭胸肺窗中测量的,允许通过荧光和多光谱吸收显微镜实时捕获图像;随后使用计算机分析对图像进行量化。我们通过两种方式验证了模型:1)改变吸入氧气含量后,2)通过β1 肾上腺素能受体阻滞剂美托洛尔治疗降低肺血流量后。这个强大且相对简单的系统促进了实验室大鼠的肺活体显微镜检查,用于药理学和生理学研究。