Department of Anesthesiology, Yale School of Medicine, New Haven, CT, USA.
Center for Translational Neuromedicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, 2200, Denmark; Center for Translational Neuromedicine, University of Rochester Medical Center, Rochester, NY, 14642, USA.
Curr Opin Neurobiol. 2022 Feb;72:15-21. doi: 10.1016/j.conb.2021.07.006. Epub 2021 Aug 15.
Small vessel disease (SVD) is a common instigator of dementia in the aging population. The hallmarks of SVD are enlargement of the perivascular spaces and white matter hyperintensities. The latter represents local fluid accumulation in white matter that either subsides or develops into lacunar infarcts. We here propose that failure of brain fluid transport-via the glymphatic system-plays a key role in initiation and progression of SVD. Our major case for this concept is that perivascular spaces are utilized as waterways for influx of cerebrospinal fluid. Stagnation of glymphatic transport may drive loss of brain fluid homeostasis leading to transient white matter edema, perivascular dilation, and ultimately demyelination. This review will discuss how glymphatic rodent studies of hypertension and diabetes have provided new insight into the pathogenesis of SVD.
小血管疾病(SVD)是老年人群中痴呆的常见诱因。SVD 的特征是血管周围间隙扩大和脑白质高信号。后者代表脑白质中局部液体的积聚,可消退或发展为腔隙性梗死。我们在此提出,脑内液体运输的失败——通过神经胶质淋巴系统——在 SVD 的发生和进展中起着关键作用。我们支持这一概念的主要依据是,血管周围间隙被用作脑脊髓液流入的水道。神经胶质淋巴系统运输的停滞可能导致脑内液体动态平衡的丧失,导致短暂性脑白质水肿、血管周围扩张,并最终导致脱髓鞘。这篇综述将讨论高血压和糖尿病的神经胶质淋巴系统啮齿动物研究如何为 SVD 的发病机制提供新的见解。