Department of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, USA.
Phys Med Biol. 2010 Jun 21;55(12):3451-65. doi: 10.1088/0031-9155/55/12/012. Epub 2010 May 28.
A common approach to quantify gadolinium (Gd) contrast agents involves measuring the post-contrast change in T1 rate and then using the constant T1 relaxivity R to determine the contrast agent concentration. Because this method is fast and non-invasive, it could be potentially valuable in many areas of brain research. However, to accurately measure contrast agent concentrations in the brain, the T1 relaxivity R of the specific agent must be accurately known. Furthermore, the macromolecular content and compartmentalization of the brain extracellular space (ECS) are expected to significantly alter R from values measured in aqueous solutions. In this study, the T1 relaxivity R of gadolinium-diethylene-triamine penta-acetic acid (Gd-DTPA) was measured following direct interstitial infusions of three different contrast agent concentrations to the parenchyma of rat brains. Changes in magnetic resonance (MR) T1 values were compared to brain slice concentrations determined with inductively coupled plasma atomic emission spectroscopy (ICP-AES) to determine R in 15 rats. Additionally, samples of cerebrospinal fluid, blood and urine were analyzed to evaluate possible Gd-DTPA clearance from the brain. The T1 relaxivity R of Gd-DTPA in the brain ECS was measured to be 5.35 (mM s)(-1) in a 2.4 T field. This value is considerably higher than estimations used in studies by other groups. Measurements of brain Gd-DTPA tissue concentrations using MRI and ICP-AES demonstrated a high degree of coincidence. Clearance of Gd-DTPA was minimal at the time point immediately after infusion. These results suggest that the environment of the brain does in fact significantly affect Gd T1 relaxivity, and that MRI can accurately measure contrast agent concentrations when this relaxivity is well characterized.
一种常见的定量钆(Gd)对比剂的方法涉及测量对比后 T1 率的变化,然后使用常数 T1 弛豫率 R 来确定对比剂浓度。由于这种方法快速且非侵入性,因此它在许多脑研究领域可能具有潜在价值。然而,为了准确测量脑内对比剂浓度,必须准确知道特定对比剂的 T1 弛豫率 R。此外,脑细胞外空间(ECS)的大分子含量和区室化预计会显著改变在水溶液中测量的值 R。在这项研究中,通过直接向大鼠脑实质内注入三种不同浓度的对比剂,测量了钆二乙三胺五乙酸(Gd-DTPA)的 T1 弛豫率 R。将磁共振(MR)T1 值的变化与通过电感耦合等离子体原子发射光谱法(ICP-AES)确定的脑切片浓度进行比较,以确定 15 只大鼠中的 R。此外,还分析了脑脊液、血液和尿液样本,以评估 Gd-DTPA 从大脑清除的可能性。在 2.4 T 场中,Gd-DTPA 在脑 ECS 中的 T1 弛豫率 R 测量值为 5.35(mM s)(-1)。这个值比其他研究小组使用的估计值高得多。使用 MRI 和 ICP-AES 测量脑 Gd-DTPA 组织浓度显示出高度一致性。在输注后立即的时间点,Gd-DTPA 的清除率非常低。这些结果表明,脑的环境确实会显著影响 Gd T1 弛豫率,并且当这种弛豫率得到很好地描述时,MRI 可以准确测量对比剂浓度。