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Observation of bi-exponential T 1ρ relaxation of in-vivo rat muscles at 3T

机译:3T时体内大鼠肌肉的双指数T1ρ松弛观察

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Background: Spin-lattice relaxation in the rotating frame, or T 1ρ relaxation, is normally described by a monoexponential decay model. However, compartmentation of tissues and microscopic molecular exchange may lead to bi-exponential or multi-exponential T 1ρ relaxation behavior in certain tissues under the application of spin lock pulse field strength. Purpose: To investigate the presence of bi-exponential T 1ρ relaxations in in-vivo rat head tissues of brain and muscle. Material and Methods: Five Sprague-Dawley rats underwent T 1ρ imaging at 3T. A B 1-insensitive rotary echo spin lock pulse was used for T 1ρ preparation with a spin lock frequency of 500Hz. Twenty-five T 1ρ-weighted images with spin lock times ranging from 1 to 60 ms were acquired using a 3D spoiled gradient echo sequence. Image intensities over different spin lock times were fitted using mono-exponential as well as biexponential models both on region-of-interest basis and pixel-by-pixel basis. F-test with a significance level P value of 0.01 was used to evaluate whether bi-exponential model gave a better fitting than monoexponential model. Results: In rat brains, only mono-exponential but no apparent bi-exponential T 1ρ relaxation (~70-71 ms) was found. In contrast, bi-exponential T 1ρ relaxation was observed in muscles of all five rats (P 10 -4). A longer and a shorter T 1ρ relaxation component were extracted to be ~37- ~ 41 ms (a fraction of ~80- ~88%) and ~9- ~11 ms (~12-20%), compared to the normal single T 1ρ relaxation of ~30- ~ 33 ms. Conclusion: Bi-exponential relaxation components were detected in rat muscles. The long and the short T 1ρ relaxation component are thought to correspond to the restricted intracellular water population and the hydrogen exchange between amine and hydroxyl groups, respectively.
机译:背景:旋转框架中的自旋晶格弛豫或T1ρ弛豫通常由单指数衰减模型描述。然而,在自旋锁定脉冲场强度的作用下,组织的分隔和微观分子交换可能导致某些组织中的双指数或多指数的T1ρ弛豫行为。目的:研究在体内大脑和肌肉的大鼠头部组织中双指数T1ρ弛豫的存在。材料和方法:五只Sprague-Dawley大鼠在3T接受了T1ρ成像。 B 1不敏感的旋转回波自旋锁定脉冲用于T1ρ制备,自旋锁定频率为500Hz。使用3D变差梯度回波序列获取了25个自旋锁定时间为1至60 ms的T1ρ加权图像。使用单指数和双指数模型,分别在关注区域和逐像素的基础上拟合了不同自旋锁定时间上的图像强度。显着性水平P值为0.01的F检验用于评估双指数模型是否比单指数模型具有更好的拟合度。结果:在大鼠大脑中,仅发现单指数的T1ρ松弛(〜70-71 ms),而没有明显的双指数的T1ρ松弛。相反,在所有五只大鼠的肌肉中均观察到双指数的T1ρ松弛(P <10 -4)。与正常单峰相比,提取的T1ρ弛豫分量的长短分别为〜37-〜41 ms(分数为〜80-〜88%)和〜9-〜11 ms(〜12-20%)。 T1ρ〜30-〜33 ms的弛豫。结论:在大鼠肌肉中检测到双指数松弛成分。长和短的T1ρ弛豫分量被认为分别对应于受限的细胞内水种群以及胺和羟基之间的氢交换。

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