Dong Yanchao, Yuan Yi, Fang Yuan, Zheng Tao, Du Dan, Gao Dawei, Du Juan, Liu Lanxiang, He Qingyuan
Department of Interventional Therapy, Qinhuangdao Municipal No. 1 Hospital, Qinhuangdao, China.
College of Electrical Engineering, Yanshan University, Qinhuangdao, China.
Int J Neurosci. 2021 Jul;131(7):666-673. doi: 10.1080/00207454.2020.1753727. Epub 2020 May 13.
Recent studies indicated that aquaporin 4 (AQP4), as the main water channel in the central nervous system (CNS), participated in the onset and progression of Parkinson's disease (PD). But how the AQP4 influenced the exacerbation of PD has not been described in detail. In this study, the effect of the AQP4 protein overexpression in nigrostriatal system that include substantia nigra (SN) and striatum (CPu) on the development of PD was investigated.
Forty male Sprague Dawley rats were equally divided into two groups at random: PD group and control group, PD group undergoing surgery and receiving 6-hydroxydopamine (6-OHDA). Using MRI tracer-based method, extracellular space (ECS) diffusion parameters of nigrostriatal system for all rats were measured, including the clearance coefficient (k') and the half-life (t). Immunohistochemistry of AQP4 was performed for 20 rats.
The area of dark-stained AQP4 immunoreactivity increased markedly in SN of PD rats, there were significant differences between two groups (SN: = 5.809, < 0.0001; CPu: = 5.943, < 0.0001). And the diffusion parameters were significantly greater in PD group than that of control group, including k' (SN: = 5.519, < 0.0001; CPu: = 2.149, = 0.045) and t (SN: = 6.131, < 0.0001; CPu: = 6.708, < 0.0001). There was a significant positive correlation between the AQP4 expression level and the k' values (SN: = 0.827, = 0.0031; CPu: = 0.641, = 0.0046), and a significant negative correlation between AQP4 and the t values (SN: r=-0.654, = 0.0403; CPu: r=-0.664, = 0.0362).
The results indicated that AQP4 expression was increased in nigrostriatal system of PD rats, therefore, the overexpression of AQP4 led to acceleration of the diffusion and drainage process of drugs in ECS, reduced the effect of drugs for the treatment of PD, inhibited the development of PD.
近期研究表明,水通道蛋白4(AQP4)作为中枢神经系统(CNS)中的主要水通道,参与了帕金森病(PD)的发生和发展。但AQP4如何影响PD的病情加重尚未详细描述。在本研究中,研究了黑质纹状体系统(包括黑质(SN)和纹状体(CPu))中AQP4蛋白过表达对PD发展的影响。
40只雄性Sprague Dawley大鼠随机等分为两组:PD组和对照组,PD组接受手术并注射6-羟基多巴胺(6-OHDA)。采用基于MRI示踪剂的方法,测量所有大鼠黑质纹状体系统的细胞外间隙(ECS)扩散参数,包括清除系数(k')和半衰期(t)。对20只大鼠进行AQP4免疫组织化学检测。
PD大鼠SN中AQP4免疫反应性深染面积明显增加,两组间差异有统计学意义(SN: = 5.809, < 0.0001;CPu: = 5.943, < 0.0001)。且PD组的扩散参数明显大于对照组,包括k'(SN: = 5.519, < 0.0001;CPu: = 2.149, = 0.045)和t(SN: = 6.131, < 0.0001;CPu: = 6.708, < 0.0001)。AQP4表达水平与k'值之间存在显著正相关(SN: = 0.827, = 0.0031;CPu: = 0.641, = 0.0046),AQP4与t值之间存在显著负相关(SN:r = -0.654, = 0.0403;CPu:r = -0.664, = 0.0362)。
结果表明,PD大鼠黑质纹状体系统中AQP4表达增加,因此,AQP4过表达导致药物在ECS中的扩散和排泄过程加速,降低了药物治疗PD的效果,抑制了PD的发展。