Cochran Blake J, Ryder William J, Parmar Arvind, Klaeser Kerstin, Reilhac Anthonin, Angelis Georgios I, Meikle Steven R, Barter Philip J, Rye Kerry-Anne
School of Medical Sciences, Faculty of Medicine, UNSW Australia;
Department of Nuclear Medicine, Concord Hospital; National Imaging Facility, University of Sydney; Brain and Mind Centre, University of Sydney; Faculty of Health Sciences, University of Sydney.
J Vis Exp. 2017 May 2(123):55184. doi: 10.3791/55184.
This paper describes the use of F-FDG and micro-PET/CT imaging to determine in vivo glucose metabolism kinetics in mice (and is transferable to rats). Impaired uptake and metabolism of glucose in multiple organ systems due to insulin resistance is a hallmark of type 2 diabetes. The ability of this technique to extract an image-derived input function from the vena cava using an iterative deconvolution method eliminates the requirement of the collection of arterial blood samples. Fitting of tissue and vena cava time activity curves to a two-tissue, three compartment model permits the estimation of kinetic micro-parameters related to the F-FDG uptake from the plasma to the intracellular space, the rate of transport from intracellular space to plasma and the rate of F-FDG phosphorylation. This methodology allows for multiple measures of glucose uptake and metabolism kinetics in the context of longitudinal studies and also provides insights into the efficacy of therapeutic interventions.
本文描述了使用F-FDG和微型PET/CT成像来测定小鼠体内葡萄糖代谢动力学(该方法也可应用于大鼠)。胰岛素抵抗导致多器官系统中葡萄糖摄取和代谢受损是2型糖尿病的一个标志。该技术利用迭代反卷积方法从腔静脉提取图像衍生输入函数的能力,消除了采集动脉血样的需求。将组织和腔静脉时间-活性曲线拟合到双组织三室模型,能够估计与F-FDG从血浆摄取到细胞内空间、从细胞内空间转运到血浆的速率以及F-FDG磷酸化速率相关的动力学微观参数。这种方法允许在纵向研究中对葡萄糖摄取和代谢动力学进行多次测量,还能深入了解治疗干预的效果。