Zhang Yu, Song Jian, He Xu-Zhong, Xiong Jian, Xue Rong, Ge Jia-Hao, Lu Shi-Yu, Hu Die, Zhang Guo-Xing, Xu Guang-Yin, Wang Lin-Hui
Department of Physiology and Neurobiology, Medical College of Soochow University, Suzhou, 215123, China.
Institute of Medical Biotechnology, Suzhou Vocational Health College, Suzhou, 215009, China.
Neurosci Bull. 2020 Dec;36(12):1524-1537. doi: 10.1007/s12264-020-00548-w. Epub 2020 Jul 25.
Following intrathecal injection of fluorescent tracers, ex vivo imaging of brain vibratome slices has been widely used to study the glymphatic system in the rodent brain. Tracer penetration into the brain is usually quantified by image-processing, even though this approach requires much time and manual operation. Here, we illustrate a simple protocol for the quantitative determination of glymphatic activity using spectrophotofluorometry. At specific time-points following intracisternal or intrastriatal injection of fluorescent tracers, certain brain regions and the spinal cord were harvested and tracers were extracted from the tissue. The intensity of tracers was analyzed spectrophotometrically and their concentrations were quantified from standard curves. Using this approach, the regional and dynamic delivery of subarachnoid CSF tracers into the brain parenchyma was assessed, and the clearance of tracers from the brain was also determined. Furthermore, the impairment of glymphatic influx in the brains of old mice was confirmed using our approach. Our method is more accurate and efficient than the imaging approach in terms of the quantitative determination of glymphatic activity, and this will be useful in preclinical studies.
鞘内注射荧光示踪剂后,脑振动切片的离体成像已被广泛用于研究啮齿动物大脑中的类淋巴系统。尽管这种方法需要大量时间和人工操作,但示踪剂在大脑中的渗透通常通过图像处理来量化。在这里,我们阐述了一种使用分光荧光测定法定量测定类淋巴活性的简单方案。在脑池内或纹状体内注射荧光示踪剂后的特定时间点,采集特定脑区和脊髓,从组织中提取示踪剂。用分光光度法分析示踪剂的强度,并根据标准曲线对其浓度进行定量。使用这种方法,评估了蛛网膜下腔脑脊液示踪剂向脑实质的区域和动态输送,并确定了示踪剂从脑中的清除情况。此外,使用我们的方法证实了老年小鼠大脑中类淋巴流入的受损情况。在类淋巴活性的定量测定方面,我们的方法比成像方法更准确、更有效,这将在临床前研究中有用。