Sleep Restriction Impairs Blood–Brain Barrier Function

The blood–brain barrier (BBB) is a large regulatory and exchange interface between the brain and peripheral circulation. We propose that changes of the BBB contribute to many pathophysiological processes in the brain of subjects with chronic sleep restriction (CSR). To achieve CSR that mimics a comm...

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Published inThe Journal of neuroscience Vol. 34; no. 44; pp. 14697 - 14706
Main Authors He, Junyun, Hsuchou, Hung, He, Yi, Kastin, Abba J., Wang, Yuping, Pan, Weihong
Format Journal Article
LanguageEnglish
Published United States Society for Neuroscience 29.10.2014
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Summary:The blood–brain barrier (BBB) is a large regulatory and exchange interface between the brain and peripheral circulation. We propose that changes of the BBB contribute to many pathophysiological processes in the brain of subjects with chronic sleep restriction (CSR). To achieve CSR that mimics a common pattern of human sleep loss, we quantified a new procedure of sleep disruption in mice by a week of consecutive sleep recording. We then tested the hypothesis that CSR compromises microvascular function. CSR not only diminished endothelial and inducible nitric oxide synthase, endothelin1, and glucose transporter expression in cerebral microvessels of the BBB, but it also decreased 2-deoxy-glucose uptake by the brain. The expression of several tight junction proteins also was decreased, whereas the level of cyclooxygenase-2 increased. This coincided with an increase of paracellular permeability of the BBB to the small tracers sodium fluorescein and biotin. CSR for 6 d was sufficient to impair BBB structure and function, although the increase of paracellular permeability returned to baseline after 24 h of recovery sleep. This merits attention not only in neuroscience research but also in public health policy and clinical practice.
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Author contributions: W.P. designed research; J.H., H.H., Y.H., Y.W., and W.P. performed research; J.H., H.H., Y.H., and W.P. contributed unpublished reagents/analytic tools; J.H., H.H., A.J.K., and W.P. analyzed data; A.J.K. and W.P. wrote the paper.
ISSN:0270-6474
1529-2401
1529-2401
DOI:10.1523/JNEUROSCI.2111-14.2014