Zheng Shaokuan, Xia Yang
Department of Physics and Center for Biomedical Research, Oakland University, Rochester, MI 48309, USA.
J Magn Reson. 2009 Jun;198(2):188-96. doi: 10.1016/j.jmr.2009.02.005. Epub 2009 Feb 21.
The multi-components of T2 relaxation in cartilage and tendon were investigated by microscopic MRI (microMRI) at 13 and 26 microm transverse resolutions. Two imaging protocols were used to quantify T2 relaxation in the specimens, a 5-point sampling and a 60-point sampling. Both multi-exponential and non-negative-least-square (NNLS) fitting methods were used to analyze the microMRI signal. When the imaging voxel size was 6.76 x 10(-4)mm3 and within the limit of practical signal-to-noise ratio (SNR) in microscopic imaging experiments, we found that (1) canine tendon has multiple T2 components; (2) bovine nasal cartilage has a single T2 component; and (3) canine articular cartilage has a single T2 component. The T2 profiles from both 5-point and 60-point methods were found to be consistent in articular cartilage. In addition, the depletion of the glycosaminoglycan component in cartilage by the trypsin digestion method was found to result in a 9.81-20.52% increase in T2 relaxation in articular cartilage, depending upon the angle at which the tissue specimen was oriented in the magnetic field.
通过微观磁共振成像(microMRI)在13微米和26微米横向分辨率下研究了软骨和肌腱中T2弛豫的多组分。使用两种成像方案对标本中的T2弛豫进行定量,即五点采样和六十点采样。多指数拟合方法和非负最小二乘法(NNLS)均用于分析微观磁共振成像信号。当成像体素大小为6.76×10⁻⁴mm³且在微观成像实验的实际信噪比(SNR)范围内时,我们发现:(1)犬肌腱具有多个T2组分;(2)牛鼻软骨具有单个T2组分;(3)犬关节软骨具有单个T2组分。发现五点法和六十点法得到的关节软骨T2图谱是一致的。此外,发现通过胰蛋白酶消化法去除软骨中的糖胺聚糖成分会导致关节软骨中T2弛豫增加9.81% - 20.52%,这取决于组织标本在磁场中的取向角度。