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Test of the glymphatic hypothesis demonstrates diffusive and aquaporin-4-independent solute transport in rodent brain parenchyma

机译:对淋巴假说的检验表明在啮齿动物的脑实质中存在弥散性和不依赖水通道蛋白4的溶质转运

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摘要

Transport of solutes through brain involves diffusion and convection. The importance of convective flow in the subarachnoid and paravascular spaces has long been recognized; a recently proposed ‘glymphatic’ clearance mechanism additionally suggests that aquaporin-4 (AQP4) water channels facilitate convective transport through brain parenchyma. Here, the major experimental underpinnings of the glymphatic mechanism were re-examined by measurements of solute movement in mouse brain following intracisternal or intraparenchymal solute injection. We found that: (i) transport of fluorescent dextrans in brain parenchyma depended on dextran size in a manner consistent with diffusive rather than convective transport; (ii) transport of dextrans in the parenchymal extracellular space, measured by 2-photon fluorescence recovery after photobleaching, was not affected just after cardiorespiratory arrest; and (iii) Aqp4 gene deletion did not impair transport of fluorescent solutes from sub-arachnoid space to brain in mice or rats. Our results do not support the proposed glymphatic mechanism of convective solute transport in brain parenchyma.
机译:溶质通过大脑的运输涉及扩散和对流。长期以来,人们认识到在蛛网膜下腔和血管旁空间中对流的重要性。最近提出的“淋巴”清除机制还表明,aquaporin-4(AQP4)水通道有助于通过脑实质进行对流运输。在这里,通过测量脑池内或实质内溶质注射后小鼠脑中溶质运动的测量,重新检查了淋巴机制的主要实验基础。我们发现:(i)荧光葡聚糖在脑实质中的运输取决于葡聚糖的大小,其方式与扩散而非对流运输一致; (ii)右心室骤停后,不影响右旋糖酐在实质细胞外空间中的运输,通过光漂白后的2-光子荧光恢复来测量; (iii)Aqp4基因缺失不会损害荧光溶质从蛛网膜下腔向小鼠或大鼠的脑内转运。我们的结果不支持脑实质中对流溶质运输的拟议的淋巴机制。

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