| Literature DB >> 27481936 |
Iben Lundgaard1, Minh Lon Lu1,2, Ezra Yang1, Weiguo Peng1, Humberto Mestre1, Emi Hitomi1, Rashid Deane1, Maiken Nedergaard1,3.
Abstract
Brain lactate concentration is higher during wakefulness than in sleep. However, it is unknown why arousal is linked to an increase in brain lactate and why lactate declines within minutes of sleep. Here, we show that the glymphatic system is responsible for state-dependent changes in brain lactate concentration. Suppression of glymphatic function via acetazolamide treatment, cisterna magna puncture, aquaporin 4 deletion, or changes in body position reduced the decline in brain lactate normally observed when awake mice transition into sleep or anesthesia. Concurrently, the same manipulations diminished accumulation of lactate in cervical, but not in inguinal lymph nodes when mice were anesthetized. Thus, our study suggests that brain lactate is an excellent biomarker of the sleep-wake cycle and increases further during sleep deprivation, because brain lactate is inversely correlated with glymphatic-lymphatic clearance. This analysis provides fundamental new insight into brain energy metabolism by demonstrating that glucose that is not fully oxidized can be exported as lactate via glymphatic-lymphatic fluid transport.Entities:
Keywords: Metabolism; astrocytes; cerebrospinal fluid; glymphatic system; lactate; stroke
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Year: 2016 PMID: 27481936 PMCID: PMC5464705 DOI: 10.1177/0271678X16661202
Source DB: PubMed Journal: J Cereb Blood Flow Metab ISSN: 0271-678X Impact factor: 6.200