Morrissey S P, Stodal H, Zettl U, Simonis C, Jung S, Kiefer R, Lassmann H, Hartung H P, Haase A, Toyka K V
Department of Neurology, Julius- Maximilians-University, Würzburg, Germany.
Brain. 1996 Feb;119 ( Pt 1):239-48. doi: 10.1093/brain/119.1.239.
In vivo proton MRI was carried out on a 7 Tesla system at 2-3 day intervals over 10 days in rats with adoptive transfer experimental allergic encephalomyelitis (AT-EAE), an animal model of some aspects of multiple sclerosis. In order to assess the integrity of the blood-brain barrier (BBB), MRI was performed by acquiring quantitative MR-relaxation time T1 images of the AT-EAE rat brain before and after i.v. injection gadolinium-diethylene triaminepentaacetic acid (Gd-DTPA) using an ultrafast MRI technique. The MRI findings were compared with the immunohistochemical stain of T cells, macrophages and albumin and, in addition, apoptosis of T cells was assessed using in situ nick translation (ISNT). Prior to injection of Gd-DTPA, an increase of T1 times in the brain of the AT-EAE rats was observed, which paralleled the time course of albumin in histological sections. These were MRI findings observed well before the onset of major cellular infiltration and before the onset of clinical signs. After i.v. injection of Gd-DTPA the observed decrease of T1 times paralleled macrophage activation, and less closely T-cell infiltration. Our results provide evidence that using MRI, it is possible to assess quantitatively the breach of the BBB and to distinguish in vivo between two components of the early phase of the lesion, inflammatory infiltrates and vasogenic oedema.
在过继转移实验性自身免疫性脑脊髓炎(AT-EAE,多发性硬化某些方面的动物模型)大鼠中,于7特斯拉系统上每隔2 - 3天进行一次体内质子磁共振成像(MRI),持续10天。为评估血脑屏障(BBB)的完整性,采用超快MRI技术,在静脉注射钆 - 二乙烯三胺五乙酸(Gd-DTPA)前后,对AT-EAE大鼠脑进行定量MR弛豫时间T1图像的MRI检查。将MRI结果与T细胞、巨噬细胞和白蛋白的免疫组织化学染色结果进行比较,此外,使用原位缺口平移法(ISNT)评估T细胞的凋亡情况。在注射Gd-DTPA之前,观察到AT-EAE大鼠脑内T1时间增加,这与组织学切片中白蛋白的时间进程平行。这些MRI结果在主要细胞浸润开始之前以及临床症状出现之前就已观察到。静脉注射Gd-DTPA后,观察到的T1时间减少与巨噬细胞活化平行,与T细胞浸润的相关性稍弱。我们的结果表明,利用MRI能够定量评估血脑屏障的破坏情况,并在体内区分病变早期的两种成分,即炎性浸润和血管源性水肿。