Zhang Wenzhong, Zhang Li, Liu Limin, Wang Xiaomin
Department of Neurobiology, Capital Medical University, Beijing 100069, PR China; Key Laboratory for Neurodegenerative Disorders of the Ministry of Education, Beijing 100069, PR China.
Department of Physiology, Capital Medical University, Beijing 100069, PR China; Key Laboratory for Neurodegenerative Disorders of the Ministry of Education, Beijing 100069, PR China.
Behav Brain Res. 2017 Jun 15;328:130-137. doi: 10.1016/j.bbr.2017.03.046. Epub 2017 Apr 5.
Diffusion tensor imaging (DTI) is a non-invasive magnetic resonance imaging technique that can be used to assess microstructural changes in a brain disease such as Parkinson's disease (PD). Fractional anisotropy (FA) is a commonly used parameter in DTI analysis, although properties of DTI/FA in analyzing brain modifications in PD have been poorly profiled. This study was thus designed to characterize the detailed time course of FA in the substantia nigra (SN). A rat model of PD was induced by microinfusion of 6-OHDA into the right medial forebrain bundle. DTI was performed before and 3, 7, 14, and 28days after 6-OHDA lesions. Locomotor behavior and apomorphine-induced rotational behavior were tested the next day after DTI except for the day 3 after lesions. Immunohistochemistry was performed to confirm the loss of tyrosine hydroxylase positive neurons and gliosis. A time-dependent and V-shape change in FA values in the SN was observed in PD rats. Following 6-OHDA lesions, FA values were initially decreased and then recovered. A maximal reduction of FA values was reached at 7days after lesions. At the same time point, a significant linear correlation between reduced FA values and impaired motor activity was observed. Our results establish the temporal property of DTI and suggest that DTI is a useful tool in evaluating the dopamine lesion in the SN in the early phase of PD. The use of DTI may thus facilitate the early diagnosis of PD in clinical practice.
扩散张量成像(DTI)是一种非侵入性磁共振成像技术,可用于评估帕金森病(PD)等脑部疾病中的微观结构变化。分数各向异性(FA)是DTI分析中常用的参数,尽管DTI/FA在分析PD脑部改变方面的特性尚未得到充分描述。因此,本研究旨在描述黑质(SN)中FA的详细时间进程。通过向右侧内侧前脑束微量注射6-羟基多巴胺(6-OHDA)诱导建立大鼠PD模型。在6-OHDA损伤前以及损伤后3、7、14和28天进行DTI检查。除损伤后第3天外,在DTI检查后的第二天测试运动行为和阿扑吗啡诱导的旋转行为。进行免疫组织化学以确认酪氨酸羟化酶阳性神经元的丧失和胶质增生。在PD大鼠中观察到SN中FA值呈时间依赖性的V形变化。6-OHDA损伤后,FA值最初下降,然后恢复。损伤后7天达到FA值的最大降低。在同一时间点,观察到FA值降低与运动活动受损之间存在显著的线性相关性。我们的结果确立了DTI的时间特性,并表明DTI是评估PD早期SN中多巴胺损伤的有用工具。因此,DTI的应用可能有助于临床实践中PD的早期诊断。