正常小鼠肝胆解剖功能显微成像X射线断层扫描和狭缝平面闪烁照相

C. Goetz , P. Choquet , L. Monassier , E. Breton , L. Elfertak , A. Constantinesco
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引用次数: 2

摘要

目的建立正常小鼠肝胆功能显像的数据采集和处理方法。材料与方法采用小型动物专用伽玛相机对11只雌性成年CD1小鼠进行了麻醉后的显像研究。注射Tc-99m甲溴非宁后获得40帧动态序列,每帧1分钟。两个个体使用x射线微型ct和注射造影剂进行断层密度形态学采集,并有助于选择感兴趣的扫描区域。四种分析模型:校正和反卷积肝图(A)、双室室模型(B)、快速动力学室室模型(C)和析因分析(D)应用于从感兴趣区域开始的以心腔和肝脏为中心的星图数据。结果甲溴非宁的最大tmax时间为4.5 ~ 4.6 min,重心tcdg时间为6.2 ~ 7.0 min,指数衰减半衰期t1/2decr为5.4 ~ 6.8 min,肝萃取率为100%。双室模型的摄取和排泄半衰期分别为2.3和5.8 min,快速动力学室模型的半衰期分别为3.2和3.3 min。比较没有发现左右肝之间、模型A、B、C和D之间摄取时间常数以及模型A、B和D之间排泄时间常数的显著差异。结论采用不同的室室模型,获得了正常CD1小鼠肝胆功能的参考值。
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Micro-imagerie anatomofonctionelle hépatobiliaire de la souris normale par tomodensitométrie X et scintigraphie planaire sténopée

Objective

Develop the methodology of data acquisition and processing for functional hepatobiliary scintigraphic imaging in normal mice.

Material and methods

The scintigraphic study was done on 11 female adult CD1 mice under gazeous anaesthesia using a small animal dedicated gamma-camera. A dynamic serie of 40 frames with 1 minute per frame was acquired after injection of Tc-99m mebrofenin. Two individuals were used for tomodensitometric morphological acquisitions using an X-ray micro-CT and the injection of a contrast agent and contributed to the choice of the scintigraphic regions of interest. Four analytical models: corrected and deconvolved hepatogram (A), bi-compartmental model (B), fast kinetics compartmental model (C) and factorial analysis (D) were applied to the scintigraphic data starting from areas of interest centered to the cardiac cavities and the liver.

Results

The mebrofenin kinetics is characterized by a time of the maximum tmax ranging between 4.5 and 4.6 min, a time of the center of gravity tcdg from 6.2 to 7.0 min, a half-life of exponential decay t1/2decr from 5.4 to 6.8 min, a fraction of hepatic extraction of 100%. Uptake and excretion half-lives are 2.3 and 5.8 min for the bicompratmental model and are 3.2 and 3.3 min for the fast kinetics compartmental model. Comparisons do not find significant differences between the right and left livers nor between models A, B, C and D for uptake time constants nor between models A, B and D for excretion time constants.

Conclusion

Reference values of hepatobiliary function in normal CD1 mice were obtained using different compartmental models.

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