Cerebral Arterial Pulsation Drives Paravascular CSF-Interstitial Fluid Exchange in the Murine Brain

被引:864
作者
Iliff, Jeffrey J. [1 ,2 ]
Wang, Minghuan [1 ,3 ]
Zeppenfeld, Douglas M. [1 ,2 ]
Venkataraman, Arun [1 ]
Plog, Benjamin A. [1 ]
Liao, Yonghong [1 ]
Deane, Rashid [1 ]
Nedergaard, Maiken [1 ]
机构
[1] Univ Rochester, Med Ctr, Ctr Translat Neuromed, Dept Neurosurg, Rochester, NY 14642 USA
[2] Oregon Hlth & Sci Univ, Dept Anesthesiol & Perioperat Med, Portland, OR 97239 USA
[3] Huazhong Univ Sci & Technol, Tongii Hosp, Tongii Med Coll, Dept Neurol, Wuhan 430030, Peoples R China
基金
美国国家卫生研究院;
关键词
CEREBROSPINAL-FLUID; AMYLOID ANGIOPATHY; WILLIS ATHEROSCLEROSIS; BULK FLOW; CLEARANCE; HYPOPERFUSION; PATHOLOGY; PATHWAY; CIRCLE; BLOOD;
D O I
10.1523/JNEUROSCI.1592-13.2013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
CSF from the subarachnoid space moves rapidly into the brain along paravascular routes surrounding penetrating cerebral arteries, exchanging with brain interstitial fluid (ISF) and facilitating the clearance of interstitial solutes, such as amyloid beta, in a pathway that we have termed the "glymphatic" system. Prior reports have suggested that paravascular bulk flow of CSF or ISF may be driven by arterial pulsation. However, cerebral arterial pulsation could not be directly assessed. In the present study, we use in vivo two-photon microscopy in mice to visualize vascular wall pulsatility in penetrating intracortical arteries. We observed that unilateral ligation of the internal carotid artery significantly reduced arterial pulsatility by similar to 50%, while systemic administration of the adrenergic agonist dobutamine increased pulsatility of penetrating arteries by similar to 60%. When paravascular CSF-ISF exchange was evaluated in real time using in vivo two-photon and ex vivo fluorescence imaging, we observed that internal carotid artery ligation slowed the rate of paravascular CSF-ISF exchange, while dobutamine increased the rate of paravascular CSF-ISF exchange. These findings demonstrate that cerebral arterial pulsatility is a key driver of paravascular CSF influx into and through the brain parenchyma, and suggest that changes in arterial pulsatility may contribute to accumulation and deposition of toxic solutes, including amyloid beta, in the aging brain.
引用
收藏
页码:18190 / 18199
页数:10
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