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In vivo imaging of increased oxidative stress in the liver by electron spin resonance-computed tomography.

机译:电子自旋共振计算机体层摄影术在肝脏中体内氧化应激增加的体内成像。

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The aim of this study was to investigate whether increased hepatic oxidative stress could be visualised in living animals before the onset of obvious liver injury. Acute hepatic injury was induced in mice by priming with heat-killed Corynebacterium parvum followed by injection of a low dose of lipopolysaccharide (LPS). Low frequency band electron spin resonance-computed tomography (ESR-CT) with 3-carbamoyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl (carbamoyl-PROXYL) was used to visualize hepatic oxidative stress. Biochemical and histological investigations performed 3 h after injection of LPS revealed no obvious injury to the liver. Conversely, significant hepatic oxidative stress could be detected at this time. Nitroxides such as carbamoyl-PROXYL are rapidly reduced to the corresponding hydroxylamine in vivo. resulting in the disappearance of their ESR signals. The kinetic clearance of carbamoyl-PROXYL after intravenous administration was delayed significantly in mice that had received LPS, due to impairment of the reduction system by hepatic oxidative stress. ESR-CT of the murine abdomen revealed a high intensity area of carbamoyl-PROXYL which consisted mainly of the liver and enlarged spleen. Time-course observations with ESR-CT using carbamoyl-PROXYL showed that the high intensity area in the liver disappeared rapidly due to reduction of carbamoyl-PROXYL. Three hours after LPS injection into the same mouse, ESR-CT images were obtained again by intravenous injection of carbamoyl-PROXYL. The ESR-CT images of the mouse with hepatic oxidative stress clearly showed that the high intensity area of carbamoyl-PROXYL in the liver persisted for a long period of time. This study is the first report to describe the use of in vivo ESR-CT for visualizing the state of increased oxidative stress in the liver before the onset of obvious hepatic injury.
机译:这项研究的目的是调查在明显的肝损伤发作之前是否可以在活体动物中观察到肝氧化应激的增加。先用热杀死的小棒杆菌引发,然后注射低剂量的脂多糖(LPS),在小鼠中诱发急性肝损伤。使用3-氨基甲酰基-2,2,5,5-四甲基吡咯烷-1-氧基(氨基甲酰基-PROXYL)的低频带电子自旋共振计算机断层扫描(ESR-CT)可视化肝脏的氧化应激。注射LPS后3小时进行的生化和组织学研究显示,肝脏未见明显损伤。相反,此时可以检测到明显的肝氧化应激。诸如氨基甲酰基-PROXYL的一氧化氮在体内迅速还原为相应的羟胺。导致其ESR信号消失。由于肝氧化应激对还原系统的损害,静脉内给药后氨基甲酰基-PROXYL的动力学清除明显延迟。小鼠腹部的ESR-CT显示出高强度的氨基甲酰基-PROXYL区域,主要由肝脏和脾脏肿大组成。使用氨基甲酰基-PROXYL的ESR-CT随时间变化的观察表明,由于氨基甲酰基-PROXYL的减少,肝脏中的高强度区域迅速消失。在将LPS注射到同一只小鼠中三小时后,通过静脉内注射氨基甲酰基-PROXYL再次获得ESR-CT图像。具有肝氧化应激的小鼠的ESR-CT图像清楚地表明,肝脏中氨基甲酰-PROXYL的高强度区域持续了很长时间。这项研究是第一个描述体内ESR-CT显像在明显肝损伤发生之前肝脏中氧化应激增加状态的报告。

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