Published online Jul 14, 2015. doi: 10.3748/wjg.v21.i26.8043
Peer-review started: November 23, 2014
First decision: January 22, 2015
Revised: February 13, 2015
Accepted: March 30, 2015
Article in press: March 31, 2015
Published online: July 14, 2015
Processing time: 234 Days and 12.6 Hours
AIM: To explore the potential of contrast-enhanced computed tomography (CECT) using ExiTron nano6000 for assessment of liver lesions in mouse models.
METHODS: Three mouse models of liver lesions were used: bile duct ligation (BDL), lipopolysaccharide (LPS)/D-galactosamine (D-GalN), and alcohol. After injection with the contrast agent ExiTron nano6000, the mice were scanned with micro-CT. Liver lesions were evaluated using CECT images, hematoxylin and eosin staining, and serum aminotransferase levels. Macrophage distribution in the injury models was shown by immunohistochemical staining of CD68. The in vitro studies measured the densities of RAW264.7 under different conditions by CECT.
RESULTS: In the in vitro studies, CECT provided specific and strong contrast enhancement of liver in mice. CECT could present heterogeneous images and densities of injured livers induced by BDL, LPS/D-GalN, and alcohol. The liver histology and immunochemistry of CD68 demonstrated that both dilated biliary tracts and necrosis in the injured livers could lead to the heterogeneous distribution of macrophages. The in vitro study showed that the RAW264.7 cell masses had higher densities after LPS activation.
CONCLUSION: Micro-CT with the contrast agent ExiTron nano6000 is feasible for detecting various liver lesions by emphasizing the heterogeneous textures and densities of CECT images.
Core tip: Noninvasive methods have been extensively studied for examining injuries in small animals in preclinical research. Contrast-enhanced computed tomography (CECT) with ExiTron nano6000 could detect various liver lesions by emphasizing the heterogeneous textures and densities of CECT images. The phenomenon is probably due to the changes in macrophage distribution, number, and function.