Laboratory Animal and Comparative Medicine ›› 2016, Vol. 36 ›› Issue (3): 180-185.DOI: 10.3969/j.issn.1674-5817.2016.03.004

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Non-invasive Assessment of Fulminant Liver Injury with Contrast-Enhanced Micro CT in Mice Models

LI Da-wei1, HUA Xiang-wei1, ZHANG Jiang1, YAO Ju-fang2, DAI Hui-li2, Kong Xian-ming2   

  1. 1. Department of Transplantation and Hepatic Surgery, 2. Animal Facility, RenJi Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China
  • Received:2016-01-12 Online:2016-06-25 Published:2016-06-25

Abstract: Objective To explore the potential use and mechanism of MicroCT using ExiTron nano6000 in the assessment of fulminant liver injury in mouse models. Methods Five male C57BL/6 mice were subjected to administration of LPS/D-GalN to develop model of fulminant liver injury. The mice were scanned with MicroCT before the treatment and at 3 h and 6 h after the establishment of liver injury model. The average CT value of liver were analyzed with software for future study. Twenty male mice were divided into 4 groups, 5 mice in each group: Nano 6000 group, the mice were treated with Nano 6000; PBS group, treated with PBS as control; model 3 h group and 6 h group, injected with LPS/D-GalN and sacrificed at 3 h, 6 h after the injection. Pathological damage of the liver were observed by microscope and serum ALT and AST were detected. Results MicroCT with ExiTron nano6000 as contrast agent could provided specific and clear 2 dimensions and 3 dimensions structure of liver and spleen in mice. The average CT value of liver was significantly increased at 3 h after LPS/D-GalN treatment and drop to baseline level at 6 h. In vitro experiments showed that LPS stimulation could enhance the endocytotic ability of macrophages to uptake ExiTron nano6000. Conclusions The Micro CT provided a rapid noninvasive longitudinal monitoring of fulminant liver injury in mice models and may be had good application in future research.

Key words: Fulminant liver injury, Micro CT, ExiTron nano 6000, Macrophage, Mice

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