Institute of Neuroscience and Psychology, College of Medicine, Veterinary and Life Science, University of Glasgow, Glasgow, United Kingdom.
Radiological Sciences Department, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia.
PLoS One. 2023 Mar 15;18(3):e0282955. doi: 10.1371/journal.pone.0282955. eCollection 2023.
The glymphatic system is a low resistance pathway, by which cerebrospinal fluid enters the brain parenchyma along perivascular spaces via AQP4 channels. It is hypothesised that the resulting convective flow of the interstitial fluid provides an efficient mechanism for the removal of waste toxins from the brain. Therefore, enhancing AQP4 function might protect against neurodegenerative diseases such as Alzheimer's disease (AD), in which the accumulation of harmful proteins and solutes is a hallmark feature. Here, we test the effect of a putative AQP4 facilitator, TGN-073, on glymphatic transport in a normal rat brain by employing different MRI techniques. Surgical procedures were undertaken to catheterise the cisterna magna, thereby enabling infusion of the MRI tracer. Followed by the intraperitoneal injection of either TGN-073, or the vehicle. Using a paramagnetic contrast agent (Gd-DTPA) as the MRI tracer, dynamic 3D T1 weighted imaging of the glymphatic system was undertaken over two hours. Further, the apparent diffusion coefficient was measured in different brain regions using diffusion-weighted imaging (DWI). While physiological parameters and arterial blood gas analysis were monitored continuously. We found that rats treated with TGN-073 showed the distribution of Gd-DTPA was more extensive and parenchymal uptake was higher compared with the vehicle group. Water diffusivity was increased in the brain of TGN-073 treated group, which indicates greater water flux. Also, MRI showed the glymphatic transport and distribution in the brain is naturally heterogeneous, which is consistent with previous studies. Our results indicate that compounds such as TGN-073 can improve glymphatic function in the brain. Since glymphatic impairment due to AQP4 dysfunction is potentially associated with several neurological disorders such as AD, dementia and traumatic brain injury, enhancing AQP4 functionality might be a promising therapeutic target.
水通道蛋白 4(AQP4)通道介导的脑淋巴系统是一个低阻力通路,脑脊液通过该通路沿着血管周围间隙进入脑实质。据推测,这种间质液的对流有助于将脑内废物毒素有效清除。因此,增强 AQP4 功能可能有助于预防神经退行性疾病,如阿尔茨海默病(AD),其中有害蛋白和溶质的积累是一个标志性特征。在这里,我们通过使用不同的 MRI 技术来测试一种假定的 AQP4 促进剂 TGN-073 对正常大鼠脑内的神经淋巴系统的影响。通过对枕骨大孔进行手术置管,从而能够对 MRI 示踪剂进行输注。随后对大鼠进行腹腔内注射 TGN-073 或载体。使用顺磁性对比剂(Gd-DTPA)作为 MRI 示踪剂,对神经淋巴系统进行了两个小时的动态 3D T1 加权成像。此外,还使用弥散加权成像(DWI)测量了不同脑区的表观弥散系数。同时,连续监测生理参数和动脉血气分析。我们发现,与载体组相比,用 TGN-073 处理的大鼠显示 Gd-DTPA 的分布更广泛,实质摄取更高。TGN-073 处理组脑内水扩散系数增加,表明水通量更大。此外,MRI 显示脑内神经淋巴系统的转运和分布具有天然异质性,这与之前的研究一致。我们的结果表明,像 TGN-073 这样的化合物可以改善脑内神经淋巴系统的功能。由于 AQP4 功能障碍导致的神经淋巴系统功能障碍可能与 AD、痴呆和创伤性脑损伤等多种神经疾病有关,因此增强 AQP4 功能可能是一个有前途的治疗靶点。