Kornguth S, Anderson M, Markley J L, Shedlovsky A
Department of Neurology, University of Wisconsin, Madison 53705, USA.
Neuroimage. 1994 Jun;1(3):220-9. doi: 10.1006/nimg.1994.1007.
The near-microscopic resolution of the mouse brain, by magnetic resonance imaging (MRI) at 9.4 T, permits in situ examination of the entire brain and longitudinal studies of neural development. MRI can be utilized to reveal brain structure at a resolution of 100 microns in the X, Y, and Z planes of brain, to differentiate the gray from white (myelin-rich) matter, and to reveal the ventricular compartments. The present report describes the structure of normal BALB/c mouse brain as revealed by imaging at 9.4 T and by histological stains; the structure of normal brain is compared with that from a phenylalanine hydroxylase-deficient mouse mutant line (Pah(enu2)) and those from normal littermates. The brains of patients with phenylketonuria (PKU) were reported to have demyelination and other structural abnormalities revealed by magnetic resonance imaging (MRI). Therefore, high-resolution MRI was used to examine the brain of this mutant, an animal model for the study of human phenylketonuria. Our study revealed no evidence of demyelination or other abnormalities in the brains of Pah(enu2) mice. Histologically, the mutant and normal mouse brains appear similar. This is consistent with a recent study from our laboratory which demonstrated that the histology of the brain of an untreated male patient, who died with PKU at the age of 29, was similar to control brain with the exception of changes directly related to visual blindness and seizures experienced by the patient.
通过9.4 T的磁共振成像(MRI)对小鼠大脑进行近显微分辨率成像,可对整个大脑进行原位检查,并对神经发育进行纵向研究。MRI可用于在大脑的X、Y和Z平面以100微米的分辨率揭示脑结构,区分灰质和白质(富含髓磷脂),并揭示脑室腔。本报告描述了通过9.4 T成像和组织学染色所揭示的正常BALB/c小鼠大脑的结构;将正常大脑的结构与苯丙氨酸羟化酶缺陷型小鼠突变系(Pah(enu2))以及正常同窝小鼠的大脑结构进行了比较。据报道,苯丙酮尿症(PKU)患者的大脑通过磁共振成像(MRI)显示有脱髓鞘和其他结构异常。因此,使用高分辨率MRI对该突变体(一种用于研究人类苯丙酮尿症的动物模型)的大脑进行检查。我们的研究未发现Pah(enu2)小鼠大脑中有脱髓鞘或其他异常的证据。从组织学上看,突变小鼠和正常小鼠的大脑看起来相似。这与我们实验室最近的一项研究一致,该研究表明,一名29岁死于PKU的未经治疗男性患者的大脑组织学与对照大脑相似,只是与该患者经历的视力丧失和癫痫发作直接相关的变化除外。