Wostyn Peter, Van Dam Debby, Audenaert Kurt, Killer Hanspeter Esriel, De Deyn Peter Paul, De Groot Veva
Department of Psychiatry, PC Sint-Amandus, Reigerlostraat 10, 8730, Beernem, Belgium.
Department of Biomedical Sciences, Laboratory of Neurochemistry and Behavior, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.
Fluids Barriers CNS. 2015 Jun 29;12:16. doi: 10.1186/s12987-015-0012-z.
In a recent review article titled "A new look at cerebrospinal fluid circulation", Brinker et al. comprehensively described novel insights from molecular and cellular biology as well as neuroimaging research, which indicate that cerebrospinal fluid (CSF) physiology is much more complex than previously believed. The glymphatic system is a recently defined brain-wide paravascular pathway for CSF and interstitial fluid exchange that facilitates efficient clearance of interstitial solutes, including amyloid-β, from the brain. Although further studies are needed to substantiate the functional significance of the glymphatic concept, one implication is that glymphatic pathway dysfunction may contribute to the deficient amyloid-β clearance in Alzheimer's disease. In this paper, we review several lines of evidence suggesting that the glymphatic system may also have potential clinical relevance for the understanding of glaucoma. As a clinically acceptable MRI-based approach to evaluate glymphatic pathway function in humans has recently been developed, a unique opportunity now exists to investigate whether suppression of the glymphatic system contributes to the development of glaucoma. The observation of a dysfunctional glymphatic system in patients with glaucoma would provide support for the hypothesis recently proposed by our group that CSF circulatory dysfunction may play a contributory role in the pathogenesis of glaucomatous damage. This would suggest a new hypothesis for glaucoma, which, just like Alzheimer's disease, might be considered then as an imbalance between production and clearance of neurotoxins, including amyloid-β.
在最近一篇题为《脑脊液循环的新视角》的综述文章中,布林克等人全面描述了分子和细胞生物学以及神经影像学研究的新见解,这些见解表明脑脊液(CSF)生理学比以前认为的要复杂得多。类淋巴系统是最近定义的一种全脑范围的血管周围途径,用于脑脊液和间质液的交换,有助于从大脑中有效清除间质溶质,包括淀粉样β蛋白。尽管需要进一步研究来证实类淋巴概念的功能意义,但一个暗示是类淋巴途径功能障碍可能导致阿尔茨海默病中淀粉样β蛋白清除不足。在本文中,我们综述了几条证据,表明类淋巴系统可能在青光眼的理解方面也具有潜在的临床相关性。由于最近已经开发出一种基于MRI的临床上可接受的方法来评估人类类淋巴途径功能,现在存在一个独特的机会来研究类淋巴系统的抑制是否有助于青光眼的发展。在青光眼患者中观察到类淋巴系统功能障碍将为我们小组最近提出的假设提供支持,即脑脊液循环功能障碍可能在青光眼性损伤的发病机制中起作用。这将为青光眼提出一个新的假设,就像阿尔茨海默病一样,青光眼随后可能被认为是包括淀粉样β蛋白在内的神经毒素产生与清除之间的失衡。