Center for Translational Neuromedicine, University of Rochester Medical Center, Rochester, New York, USA.
Department of Neuroscience, University of Rochester Medical Center, Rochester, New York, USA.
Glia. 2024 May;72(5):982-998. doi: 10.1002/glia.24515. Epub 2024 Feb 16.
The glymphatic system transports cerebrospinal fluid (CSF) into the brain via arterial perivascular spaces and removes interstitial fluid from the brain along perivenous spaces and white matter tracts. This directional fluid flow supports the clearance of metabolic wastes produced by the brain. Glymphatic fluid transport is facilitated by aquaporin-4 (AQP4) water channels, which are enriched in the astrocytic vascular endfeet comprising the outer boundary of the perivascular space. Yet, prior studies of AQP4 function have relied on genetic models, or correlated altered AQP4 expression with glymphatic flow in disease states. Herein, we sought to pharmacologically manipulate AQP4 function with the inhibitor AER-271 to assess the contribution of AQP4 to glymphatic fluid transport in mouse brain. Administration of AER-271 inhibited glymphatic influx as measured by CSF tracer infused into the cisterna magna and inhibited increases in the interstitial fluid volume as measured by diffusion-weighted MRI. Furthermore, AER-271 inhibited glymphatic efflux as assessed by an in vivo clearance assay. Importantly, AER-271 did not affect AQP4 localization to the astrocytic endfeet, nor have any effect in AQP4 deficient mice. Since acute pharmacological inhibition of AQP4 directly decreased glymphatic flow in wild-type but not in AQP4 deficient mice, we foresee AER-271 as a new tool for manipulation of the glymphatic system in rodent brain.
水通道蛋白 4(AQP4)介导的脑内淋巴系统通过动脉周细胞间隙向脑内转运脑脊液,并沿血管周围间隙和白质纤维束从脑内清除细胞间液。这种定向的液体流动有助于清除大脑产生的代谢废物。AQP4 水通道丰富存在于星形胶质细胞血管足突中,这些足突构成了血管周围间隙的外边界,从而促进脑内淋巴系统的液体转运。然而,先前关于 AQP4 功能的研究依赖于基因模型,或者将 AQP4 表达的改变与疾病状态下的脑内淋巴系统液体流动相关联。在此,我们试图通过抑制剂 AER-271 来药理学干预 AQP4 功能,以评估 AQP4 对小鼠脑内淋巴系统液体转运的贡献。AER-271 的给药抑制了通过脑池内注入示踪剂测量的脑内淋巴系统的内流,并抑制了扩散加权 MRI 测量的细胞间液体积的增加。此外,通过体内清除测定评估了 AER-271 对脑内淋巴系统的外排的抑制作用。重要的是,AER-271 不影响 AQP4 向星形胶质细胞足突的定位,在 AQP4 缺陷型小鼠中也没有任何作用。由于急性药理学抑制 AQP4 直接降低了野生型小鼠但没有降低 AQP4 缺陷型小鼠的脑内淋巴系统液体流动,因此我们预计 AER-271 将成为操纵啮齿动物脑内淋巴系统的新工具。