Henkelman R M, Stanisz G J, Menezes N, Burstein D
Department of Medical Biophysics, University of Toronto, Toronto, Canada.
Magn Reson Med. 2002 Dec;48(6):1081-4. doi: 10.1002/mrm.10322.
Magnetization transfer (MT) and T(1) and T(2) relaxation of normal, trypsinized, and interleukin-1beta (IL-1beta)-treated cartilage were measured in the absence and presence of Gd-DTPA(2-). Without the addition of Gd-DTPA(2-), neither T(1) nor T(2) showed any significant change with cartilage damage. However, with Gd-DTPA(2-), trypsinized cartilage exhibited substantially shorter T(1) than normal cartilage, as expected due to the glycosaminoglycan (GAG) loss in these samples, and associated increased Gd-DTPA(2-) concentration. The T(2) results were similar, but less dramatic. The MT pseudo first-order exchange rate, RM(0B), did not depend on the contrast agent concentration, as expected, and was significantly faster for trypsinized and slower for IL-1beta-treated cartilage. In both cases, the MT fraction of the macromolecular pool M(0B) decreased while only trypsinized cartilage showed an increase in MT exchange rate R. The MT ratio (MTR) decreased with increasing Gd-DTPA(2-) concentration. However, interpretation of the MTR results in the presence of Gd-DTPA(2-) was complicated due to competing effects of increased longitudinal relaxivity and MT exchange. Therefore, in a cartilage sample with an unknown degree of GAG depletion and some collagen damage, a full MT analysis might be used to probe the molecular state of cartilage, but it would not be possible to use a simple MTR measurement after the administration of Gd-DTPA(2-) to differentially determine the amount of cartilage degradation in the sample.
在不存在和存在钆二乙烯三胺五乙酸(Gd-DTPA²⁻)的情况下,测量了正常、经胰蛋白酶处理和白细胞介素-1β(IL-1β)处理的软骨的磁化传递(MT)以及T(1)和T(2)弛豫。在不添加Gd-DTPA²⁻时,T(1)和T(2)均未因软骨损伤而表现出任何显著变化。然而,在添加Gd-DTPA²⁻后,如预期的那样,由于这些样品中糖胺聚糖(GAG)的损失以及相关的Gd-DTPA²⁻浓度增加,经胰蛋白酶处理的软骨表现出比正常软骨明显更短的T(1)。T(2)的结果相似,但变化较小。MT伪一级交换率RM(0B)如预期的那样不依赖于造影剂浓度,并且经胰蛋白酶处理的软骨的RM(0B)明显更快,而经IL-1β处理的软骨的RM(0B)则较慢。在这两种情况下,大分子池M(0B)的MT分数均降低,而只有经胰蛋白酶处理的软骨显示出MT交换率R增加。MT比率(MTR)随着Gd-DTPA²⁻浓度的增加而降低。然而,在存在Gd-DTPA²⁻的情况下,由于纵向弛豫率增加和MT交换的竞争效应,对MTR结果的解释变得复杂。因此,在一个GAG消耗程度未知且存在一些胶原损伤的软骨样品中,完整的MT分析可能用于探究软骨的分子状态,但在给予Gd-DTPA²⁻后,不可能通过简单的MTR测量来差异确定样品中软骨降解的量。